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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Medical academic journal</journal-id><journal-title-group><journal-title xml:lang="en">Medical academic journal</journal-title><trans-title-group xml:lang="ru"><trans-title>Медицинский академический журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1608-4101</issn><issn publication-format="electronic">2687-1378</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">83594</article-id><article-id pub-id-type="doi">10.17816/MAJ83594</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Analytical reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Аналитические обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Molecular mechanisms of drug resistance of glial tumor of brain. Part 2: Proliferation, angiogenesis, metastasis and recurrency</article-title><trans-title-group xml:lang="ru"><trans-title>Молекулярные механизмы лекарственной устойчивости глиальных опухолей мозга. Часть 2. Пролиферация, ангиогенез, метастазирование и рецидивирование</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2464-7370</contrib-id><name-alternatives><name xml:lang="en"><surname>Chernov</surname><given-names>Alexander N.</given-names></name><name xml:lang="ru"><surname>Чернов</surname><given-names>Александр Николаевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, Cand. Sci. (Biol.), Research Associate, Department of General Pathology and Pathological Physiology</p></bio><bio xml:lang="ru"><p>канд. биол. наук, научный сотрудник отдела общей патологии и патологической физиологии</p></bio><email>al.chernov@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8773-0932</contrib-id><contrib-id contrib-id-type="scopus">24331659400</contrib-id><name-alternatives><name xml:lang="en"><surname>Galimova</surname><given-names>Elvira S.</given-names></name><name xml:lang="ru"><surname>Галимова</surname><given-names>Эльвира Сафуановна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>PhD, Cand. Sci. (Biol.), Senior Researcher; Senior Researcher</p></bio><bio xml:lang="ru"><p>канд. биол. наук, старший научный сотрудник; старший научный сотрудник</p></bio><email>elya-4@yandex.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5168-2801</contrib-id><contrib-id contrib-id-type="scopus">6603643804</contrib-id><contrib-id contrib-id-type="researcherid">F-6743-2013</contrib-id><name-alternatives><name xml:lang="en"><surname>Shamova</surname><given-names>Olga V.</given-names></name><name xml:lang="ru"><surname>Шамова</surname><given-names>Ольга Валерьевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Dr. Sci. (Biol.), Assistant Professor, Corresponding Member of the Russian Academy of Sciences, Head of the Department of General Pathology and Pathological Physiology; Professor of the Department of Biochemistry</p></bio><bio xml:lang="ru"><p>д-р биол. наук, доцент, член-корреспондент РАН, заведующий отделом общей патологии и патологической физиологии; профессор кафедры биохимии</p></bio><email>oshamova@yandex.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Institute of Experimental Medicine</institution></aff><aff><institution xml:lang="ru">Институт экспериментальной медицины</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Sechenov Institute of Evolutionary Physiology and Biochemistry Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Институт эволюционной физиологии и биохимии им. И.М. Сеченова РАН</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Saint Petersburg State University</institution></aff><aff><institution xml:lang="ru">Санкт-Петербургский государственный университет</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2022-06-28" publication-format="electronic"><day>28</day><month>06</month><year>2022</year></pub-date><pub-date date-type="pub" iso-8601-date="2022-07-19" publication-format="electronic"><day>19</day><month>07</month><year>2022</year></pub-date><volume>22</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>89</fpage><lpage>117</lpage><history><date date-type="received" iso-8601-date="2021-10-23"><day>23</day><month>10</month><year>2021</year></date><date date-type="accepted" iso-8601-date="2022-05-29"><day>29</day><month>05</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Chernov A.N., Galimova E.S., Shamova O.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Чернов А.Н., Галимова Э.С., Шамова О.В.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Chernov A.N., Galimova E.S., Shamova O.V.</copyright-holder><copyright-holder xml:lang="ru">Чернов А.Н., Галимова Э.С., Шамова О.В.</copyright-holder><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc-nd/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://journals.eco-vector.com/MAJ/article/view/83594">https://journals.eco-vector.com/MAJ/article/view/83594</self-uri><abstract xml:lang="en"><p>The main reason for the low efficiency of glioblastoma therapy is its resistance to therapeutic procedures. The development of multidrug resistance occurs as a result of the selection of tumor clones during therapy. The resistant cell clones to radiotherapy and chemotherapy can proliferate, leading to tumor growth, in which its own vascular network is formed (angiogenesis), which promotes cell migration, invasion and the appearance of metastases and recurrent glioblastoma. The review examines the relationship at the molecular level of multidrug resistance with proliferation, angiogenesis, migration, metastasis, and the formation of glioblastoma relapses, with an emphasis on identifying new targets among proteins, microRNAs, signal transduction kinases, transcription factors, tumor-supressor genes and oncogenes.</p></abstract><trans-abstract xml:lang="ru"><p>Главная причина низкой эффективности лечения глиобластомы — ее устойчивость к терапевтическим процедурам. Развитие множественной лекарственной устойчивости происходит в результате отбора опухолевых клонов во время терапии. Резистентные к радиотерапии или химиотерапии клоны клеток могут пролиферировать, приводя к росту опухоли, в которой образуется собственная сеть сосудов (ангиогенез), способствующая миграции и инвазии клеток, и, как следствие, появлению метастазов и рецидивов глиобластомы. В обзоре рассмотрена взаимосвязь на молекулярном уровне множественной лекарственной устойчивости с пролиферацией, ангиогенезом, миграцией, метастазированием и образованием рецидивов глиобластомы с акцентом на выявлении новых мишеней среди белков, микроРНК, киназ сигнальной трансдукции, транскрипционных факторов, генов-супрессоров и онкогенов.</p></trans-abstract><kwd-group xml:lang="en"><kwd>glioblastoma</kwd><kwd>multidrug resistance</kwd><kwd>chemotherapy drugs</kwd><kwd>proliferation</kwd><kwd>angiogenesis</kwd><kwd>metastasis</kwd><kwd>recurrence</kwd><kwd>growth factors</kwd><kwd>their receptors</kwd><kwd>signal transduction kinases</kwd><kwd>microRNA</kwd><kwd>transcription factors</kwd><kwd>oncogenes</kwd><kwd>suppressor genes</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>глиобластома</kwd><kwd>множественная лекарственная устойчивость</kwd><kwd>химиопрепараты</kwd><kwd>пролиферация</kwd><kwd>ангиогенез</kwd><kwd>метастазирование</kwd><kwd>рецидивирование</kwd><kwd>ростовые факторы и рецепторы</kwd><kwd>киназы сигнальной трансдукции</kwd><kwd>микроРНК</kwd><kwd>транскрипционные факторы</kwd><kwd>онкогены</kwd><kwd>гены-супрессоры опухолей</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Griffin M, Khan R, Basu S, et al. Ion channels as therapeutic targets in high grade gliomas. Cancers (Basel). 2020;12(10):3068. DOI: 10.3390/cancers12103068</mixed-citation><mixed-citation xml:lang="ru">Griffin M., Khan R., Basu S. et al. Ion channels as therapeutic targets in high grade gliomas // Cancers (Basel). 2020. Vol. 12, No. 10. P. 3068. DOI: 10.3390/cancers12103068</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Sottoriva A, Spiteri I, Piccirillo SG, et al. Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics. Proc Natl Acad Sci USA. 2013;110(10):4009–4014. DOI: 10.1073/pnas.1219747110</mixed-citation><mixed-citation xml:lang="ru">Sottoriva A., Spiteri I., Piccirillo S.G. et al. Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics // Proc. Natl. Acad. Sci. USA. 2013. Vol. 110, No. 10. P. 4009–4014. DOI: 10.1073/pnas.1219747110</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Verhaak RGW, Hoadley KA, Purdom E, et al. Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. Cancer Cell. 2010;17:98–110. DOI: 10.1016/j.ccr.2009.12.020</mixed-citation><mixed-citation xml:lang="ru">Verhaak R.G.W., Hoadley K.A., Purdom E. et al. Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1 // Cancer Cell. 2010. Vol. 17. P. 98–110. DOI: 10.1016/j.ccr.2009.12.020</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Wang Z, Zhang H, Xu S, et al. The adaptive transition of glioblastoma stem cells and its implications on treatments. Signal Transduc Target Ther. 2021;6(1):124. DOI: 10.1038/s41392-021-00491-w</mixed-citation><mixed-citation xml:lang="ru">Wang Z., Zhang H., Xu S. et al. The adaptive transition of glioblastoma stem cells and its implications on treatments // Signal Transduc. Target. Ther. 2021. Vol. 6, No. 1. P. 124. DOI: 10.1038/s41392-021-00491-w</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Mesrati MH, Behrooz B, Abuhamad AY, Syahir A. Understanding glioblastoma biomarkers: knocking a mountain with a hammer. Cells. 2020;9(5):1236. DOI: 10.3390/cells9051236</mixed-citation><mixed-citation xml:lang="ru">Mesrati M.H., Behrooz A.B., Abuhamad A.Y., Syahir A. Understanding glioblastoma biomarkers: knocking a mountain with a hammer // Cells. 2020. Vol. 9, No. 5. P. 1236. DOI: 10.3390/cells9051236</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Suvà ML, Tirosh I. The Glioma stem cell model in the era of single-cell genomics. Cancer Cell. 2020;37(5):630–636. DOI: 10.1016/j.ccell.2020.04.001</mixed-citation><mixed-citation xml:lang="ru">Suvà M.L., Tirosh I. The Glioma stem cell model in the era of single-cell genomics // Cancer Cell. 2020. Vol. 37, No. 5. P. 630–636. DOI: 10.1016/j.ccell.2020.04.001</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Park JC, Chang IB, Ahn JH, et al. Nerve growth factor stimulates glioblastoma proliferation through notch1 receptor signaling. J Korean Neurosurg Soc. 2018;61(4):441–449. DOI: 10.3340/jkns.2017.0219</mixed-citation><mixed-citation xml:lang="ru">Park J.C., Chang I.B., Ahn J.H. et al. Nerve growth factor stimulates glioblastoma proliferation through notch1 receptor signaling // J. Korean Neurosurg. Soc. 2018. Vol. 61, No. 4. P. 441–449. DOI: 10.3340/jkns.2017.0219</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Watanabe T, Katayama Y, Kimura S, Yoshino A. Control of proliferation and survival of C6 glioma cells with modification of the nerve growth factor autocrine system. J Neurooncol. 1999;41(2):121–128. DOI: 10.1023/a:1006127624487</mixed-citation><mixed-citation xml:lang="ru">Watanabe T., Katayama Y., Kimura S., Yoshino A. Control of proliferation and survival of C6 glioma cells with modification of the nerve growth factor autocrine system // J. Neurooncol. 1999. Vol. 41, No. 2. P. 121–128. DOI: 10.1023/a:1006127624487</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Garofalo S, Porzia A, Mainiero F, et al. Environmental stimuli shape microglial plasticity in glioma. Elife. 2017;6:e33415. DOI: 10.7554/eLife.33415</mixed-citation><mixed-citation xml:lang="ru">Garofalo S., Porzia A., Mainiero F. et al. Environmental stimuli shape microglial plasticity in glioma // Elife. 2017. Vol. 6. P. e33415. DOI: 10.7554/eLife.33415</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Xiong J, Zhou L, Yang M, et al. ProBDNF and its receptors are upregulated in glioma and inhibit the growth of glioma cells in vitro. Neuro Oncol. 2013;15(8):990–1007. DOI: 10.1093/neuonc/not039</mixed-citation><mixed-citation xml:lang="ru">Xiong J., Zhou L., Yang M. et al. ProBDNF and its receptors are upregulated in glioma and inhibit the growth of glioma cells in vitro // Neuro. Oncol. 2013. Vol. 15, No. 8. P. 990–1007. DOI: 10.1093/neuonc/not039</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Venkatesh HS, Johung TB, Caretti V, et al. Neuronal activity promotes glioma growth through neuroligin-3 secretion. Cell. 2015;161:803–816. DOI: 10.1016/j.cell.2015.04.012</mixed-citation><mixed-citation xml:lang="ru">Venkatesh H.S., Johung T.B., Caretti V. et al. Neuronal activity promotes glioma growth through neuroligin-3 secretion // Cell. 2015. Vol. 161. P. 803–816. DOI: 10.1016/j.cell.2015.04.012</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Venkatesh HS, Morishita W, Geraghty AC, et al. Electrical and synaptic integration of glioma into neural circuits. Nature. 2019;573:539–545. DOI: 10.1038/s41586-019-1563-y</mixed-citation><mixed-citation xml:lang="ru">Venkatesh H.S., Morishita W., Geraghty A.C. et al. Electrical and synaptic integration of glioma into neural circuits // Nature. 2019. Vol. 573. P. 539–545. DOI: 10.1038/s41586-019-1563-y</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Taylor KR, Barron T, Zhang H, et al. Glioma synapses recruit mechanisms of adaptive plasticity. BioRxiv. 2021. DOI: 10.1101/2021.11.04.467325</mixed-citation><mixed-citation xml:lang="ru">Taylor K.R., Barron T., Zhang H. et al. Glioma synapses recruit mechanisms of adaptive plasticity // BioRxiv. 2021. DOI: 10.1101/2021.11.04.467325</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Wang Y, Liu YY, Chen MB, et al. Neuronal-driven glioma growth requires Gαi1 and Gαi3. Theranostics. 2021;11(17):8535–8549. DOI: 10.7150/thno.61452</mixed-citation><mixed-citation xml:lang="ru">Wang Y., Liu Y.Y., Chen M.B. et al. Neuronal-driven glioma growth requires Gαi1 and Gαi3 // Theranostics. 2021. Vol. 11, No. 17. P. 8535–8549. DOI: 10.7150/thno.61452</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Lawn S, Krishna N, Pisklakova A, et al. Neurotrophin signaling via TrkB and TrkC receptors promotes the growth of brain tumor-initiating cells. J Biol Chem. 2015;290(6):3814–3824. DOI: 10.1074/jbc.M114.599373</mixed-citation><mixed-citation xml:lang="ru">Lawn S., Krishna N., Pisklakova A. et al. Neurotrophin signaling via TrkB and TrkC receptors promotes the growth of brain tumor-initiating cells // J. Biol. Chem. 2015. Vol. 290, No. 6. P. 3814–3824. DOI: 10.1074/jbc.M114.599373</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Wang T-C, Luo S-J, Chang S-F. Bone morphogenetic protein 7 effect on human glioblastoma cell transmigration and migration. Life (Basel). 2021;11(7):708. DOI: 10.3390/life11070708</mixed-citation><mixed-citation xml:lang="ru">Wang T.-C., Luo S.-J., Chang S.-F. Bone morphogenetic protein 7 effect on human glioblastoma cell transmigration and migration // Life (Basel). 2021. Vol. 11, No. 7. P. 708. DOI: 10.3390/life11070708</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Valter MM, Wiestler OD, Pietsche T. Differential control of VEGF synthesis and secretion in human glioma cells by IL-1 and EGF. Int J Dev Neurosci. 1999;17(5–6):565–577. DOI: 10.1016/s0736-5748(99)00048-9</mixed-citation><mixed-citation xml:lang="ru">Valter M.M., Wiestler O.D., Pietsche T. Differential control of VEGF synthesis and secretion in human glioma cells by IL-1 and EGF // Int. J. Dev. Neurosci. 1999. Vol. 17, No. 5–6. P. 565–577. DOI: 10.1016/s0736-5748(99)00048-9</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Krcek R, Matschke V, Theis V, et al. Vascular endothelial growth factor, irradiation, and axitinib have diverse effects on motility and proliferation of glioblastoma multiforme cells. Front Oncol. 2017;7:182. DOI: 10.3389/fonc.2017.00182</mixed-citation><mixed-citation xml:lang="ru">Krcek R., Matschke V., Theis V. et al. Vascular endothelial growth factor, irradiation, and axitinib have diverse effects on motility and proliferation of glioblastoma multiforme cells // Front. Oncol. 2017. Vol. 7. P. 182. DOI: 10.3389/fonc.2017.00182</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Audero E, Cascone I, Zanon I, et al. Expression of angiopoietin-1 in human glioblastomas regulates tumor-induced angiogenesis: in vivo and in vitro studies. Arterioscler Thromb Vasc Biol. 2001;21(4):536–541. DOI: 10.1161/01.atv.21.4.536</mixed-citation><mixed-citation xml:lang="ru">Audero E., Cascone I., Zanon I. et al. Expression of angiopoietin-1 in human glioblastomas regulates tumor-induced angiogenesis: in vivo and in vitro studies // Arterioscler. Thromb. Vasc. Biol. 2001. Vol. 21, No. 4. P. 536–541. DOI: 10.1161/01.atv.21.4.536</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Hu B, Guo P, Fang Q, et al. Angiopoietin-2 induces human glioma invasion through the activation of matrix metalloprotease-2. Proc Natl Acad Sci USA. 2003;100(15):8904–8909. DOI: 10.1073/pnas.1533394100</mixed-citation><mixed-citation xml:lang="ru">Hu B., Guo P., Fang Q. et al. Angiopoietin-2 induces human glioma invasion through the activation of matrix metalloprotease-2 // Proc. Natl. Acad. Sci. USA. 2003. Vol. 100, No. 15. P. 8904–8909. DOI: 10.1073/pnas.1533394100</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Hu B, Jarzynka MJ, Guo P, et al. Angiopoietin 2 induces glioma cell invasion by stimulating matrix metalloprotease 2 expression through the alphavbeta1 integrin and focal adhesion kinase signaling pathway. Cancer Res. 2006;66(2):775–783. DOI: 10.1158/0008-5472.CAN-05-1149</mixed-citation><mixed-citation xml:lang="ru">Hu B., Jarzynka M.J., Guo P. et al. Angiopoietin 2 induces glioma cell invasion by stimulating matrix metalloprotease 2 expression through the alphavbeta1 integrin and focal adhesion kinase signaling pathway // Cancer Res. 2006. Vol. 66, No. 2. P. 775–783. DOI: 10.1158/0008-5472.CAN-05-1149</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Brunckhorst MK, Wang H, Lu R, Yu Q. Angiopoietin-4 promotes glioblastoma progression by enhancing tumor cell viability and angiogenesis. Cancer Res. 2010;70(18):7283–7293. DOI: 10.1158/0008-5472.CAN-09-4125</mixed-citation><mixed-citation xml:lang="ru">Brunckhorst M.K., Wang H., Lu R., Yu Q. Angiopoietin-4 Promotes Glioblastoma Progression by Enhancing Tumor Cell Viability and Angiogenesis // Cancer Res. 2010. Vol. 70, No. 18. P. 7283–7293. DOI: 10.1158/0008-5472.CAN-09-4125</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">Chen X-C, Wei X-T, Guan J-H, et al. EGF stimulates glioblastoma metastasis by induction of matrix metalloproteinase-9 in an EGFR-dependent mechanism. Oncotarget. 2017;8(39):65969–65982. DOI: 10.18632/oncotarget.19622</mixed-citation><mixed-citation xml:lang="ru">Chen X.-C., Wei X.-T., Guan J.-H. et al. EGF stimulates glioblastoma metastasis by induction of matrix metalloproteinase-9 in an EGFR-dependent mechanism // Oncotarget. 2017. Vol. 8, No. 39. P. 65969–65982. DOI: 10.18632/oncotarget.19622</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Pudełek M, Król K, Catapano J, et al. Epidermal Growth Factor (EGF) augments the invasive potential of human glioblastoma multiforme cells via the activation of collaborative EGFR/ROS-dependent signaling. Int J Mol Sci. 2020;21(10):3605. DOI: 10.3390/ijms21103605</mixed-citation><mixed-citation xml:lang="ru">Pudełek M., Król K., Catapano J. et al. Epidermal Growth Factor (EGF) augments the invasive potential of human glioblastoma multiforme cells via the activation of collaborative EGFR/ROS-dependent signaling // Int. J. Mol. Sci. 2020. Vol. 21, No. 10. P. 3605. DOI: 10.3390/ijms21103605</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">An Z, Aksoy O, Zheng T, et al. Epidermal growth factor receptor and EGFRvIII in glioblastoma: signaling pathways and targeted therapies. Oncogene. 2018;37:1561–1575. DOI: 10.1038/s41388-017-0045-7</mixed-citation><mixed-citation xml:lang="ru">An Z., Aksoy O., Zheng T. et al. Epidermal growth factor receptor and EGFRvIII in glioblastoma: signaling pathways and targeted therapies // Oncogene. 2018. Vol. 37. P. 1561–1575. DOI: 10.1038/s41388-017-0045-7</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Garnett J, Chumbalkar V, Vaillant B, et al. Regulation of HGF expression by DeltaEGFR-mediated c-Met activation in glioblastoma cells. Neoplasia. 2013;15(1):73–84. DOI: 10.1593/neo.121536</mixed-citation><mixed-citation xml:lang="ru">Garnett J., Chumbalkar V., Vaillant B. et al. Regulation of HGF expression by DeltaEGFR-mediated c-Met activation in glioblastoma cells // Neoplasia. 2013. Vol. 15, No. 1. P. 73–84. DOI: 10.1593/neo.121536</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Jimenez-Pascual A, Siebzehnrubl FA. Fibroblast growth factor receptor functions in glioblastoma. Cells. 2019;8(7):715. DOI: 10.3390/cells8070715</mixed-citation><mixed-citation xml:lang="ru">Jimenez-Pascual A., Siebzehnrubl F.A. Fibroblast growth factor receptor functions in glioblastoma // Cells. 2019. Vol. 8, No. 7. P. 715. DOI: 10.3390/cells8070715</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Jimenez-Pascual A, Mitchell K, Siebzehnrubl FA, Lathia JD. FGF2: a novel druggable target for glioblastoma? Expert Opin Ther Targets. 2020;24(4):311–318. DOI: 10.1080/14728222.2020.1736558</mixed-citation><mixed-citation xml:lang="ru">Jimenez-Pascual A., Mitchell K., Siebzehnrubl F.A., Lathia J.D. FGF2: a novel druggable target for glioblastoma? // Expert. Opin. Ther. Targets. 2020. Vol. 24, No. 4. P. 311–318. DOI: 10.1080/14728222.2020.1736558</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">Tiong KH, Mah LY, Leong CO. Functional roles of fibroblast growth factor receptors (FGFRs) signaling in human cancers. Apoptosis. 2013;18(12):1447–1468. DOI: 10.1007/s10495-013-0886-7</mixed-citation><mixed-citation xml:lang="ru">Tiong K.H., Mah L.Y., Leong C.O. Functional roles of fibroblast growth factor receptors (FGFRs) signaling in human cancers // Apoptosis. 2013. Vol. 18, No. 12. P. 1447–1468. DOI: 10.1007/s10495-013-0886-7</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Tirrò E, Massimino M, Romano C, et al. Prognostic and therapeutic roles of the insulin growth factor system in glioblastoma. Front Oncol. 2021;10:612385. DOI: 10.3389/fonc.2020.612385</mixed-citation><mixed-citation xml:lang="ru">Tirrò E., Massimino M., Romano C. et al. Prognostic and therapeutic roles of the insulin growth factor system in glioblastoma // Front. Oncol. 2021. Vol. 10. P. 612385. DOI: 10.3389/fonc.2020.612385</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">Maris C, D’Haene N, Trepant AL, et al. IGF-IR: a new prognostic biomarker for human glioblastoma. Br J Cancer. 2015;113(5):729–737. DOI: 10.1038/bjc.2015.242</mixed-citation><mixed-citation xml:lang="ru">Maris C., D’Haene N., Trepant A.L. et al. IGF-IR: a new prognostic biomarker for human glioblastoma // Br. J. Cancer. 2015. Vol. 113, No. 5. P. 729–737. DOI: 10.1038/bjc.2015.242</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Simpson AD, Soo YWJ, Rieunier G, et al. Type 1 IGF receptor associates with adverse outcome and cellular radioresistance in paediatric high-grade glioma. Br J Cancer. 2020;122(5):624–629. DOI: 10.1038/s41416-019-0677-1</mixed-citation><mixed-citation xml:lang="ru">Simpson A.D., Soo Y.W.J., Rieunier G. et al. Type 1 IGF receptor associates with adverse outcome and cellular radioresistance in paediatric high-grade glioma // Br. J. Cancer. 2020. Vol. 122, No. 5. P. 624–629. DOI: 10.1038/s41416-019-0677-1</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">Cruickshanks N, Zhang Y, Yuan F, et al. Role and therapeutic targeting of the HGF/MET pathway in glioblastoma. Cancers (Basel). 2017;9(7):87. DOI: 10.3390/cancers9070087</mixed-citation><mixed-citation xml:lang="ru">Cruickshanks N., Zhang Y., Yuan F. et al. Role and therapeutic targeting of the HGF/MET pathway in glioblastoma // Cancers (Basel). 2017. Vol. 9, No. 7. P. 87. DOI: 10.3390/cancers9070087</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">Navis AC, van Lith SA, van Duijnhoven SM, et al. Identification of a novel MET mutation in high-grade glioma resulting in an auto-active intracellular protein. Acta Neuropathol. 2015;130:131–144. DOI: 10.1007/s00401-015-1420-5</mixed-citation><mixed-citation xml:lang="ru">Navis A.C., van Lith S.A., van Duijnhoven S.M. et al. Identification of a novel MET mutation in high-grade glioma resulting in an auto-active intracellular protein // Acta Neuropathol. 2015. Vol. 130. P. 131–144. DOI: 10.1007/s00401-015-1420-5</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Cantanhede IG, de Oliveira JRM. PDGF family expression in glioblastoma multiforme: data compilation from Ivy Glioblastoma Atlas Project Database. Sci Rep. 2017;7(1):15271. DOI: 10.1038/s41598-017-15045-w</mixed-citation><mixed-citation xml:lang="ru">Cantanhede I.G., de Oliveira J.R.M. PDGF family expression in glioblastoma multiforme: data compilation from Ivy Glioblastoma Atlas Project Database // Sci. Rep. 2017. Vol. 7, No. 1. P. 15271. DOI: 10.1038/s41598-017-15045-w</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">Bohm AK, DePetro J, Binding CE, et al. In vitro modeling of glioblastoma initiation using PDGF-AA and p53-null neural progenitors. Neuro Oncol. 2020;22(8):1150–1161. DOI: 10.1093/neuonc/noaa093</mixed-citation><mixed-citation xml:lang="ru">Bohm A.K., DePetro J., Binding C.E. et al. In vitro modeling of glioblastoma initiation using PDGF-AA and p53-null neural progenitors // Neuro. Oncol. 2020. Vol. 22, No. 8. P. 1150–1161. DOI: 10.1093/neuonc/noaa093</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">Clara CA, Marie SK, de Almeida JR, et al. Angiogenesis and expression of PDGF-C, VEGF, CD105 and HIF-1α in human glioblastoma. Neuropathology. 2014;34(4):343–352. DOI: 10.1111/neup.12111</mixed-citation><mixed-citation xml:lang="ru">Clara C.A., Marie S.K., de Almeida J.R. et al. Angiogenesis and expression of PDGF-C, VEGF, CD105 and HIF-1α in human glioblastoma // Neuropathology. 2014. Vol. 34, No. 4. P. 343–352. DOI: 10.1111/neup.12111</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">di Tomaso E, London N, Fuja D, et al. PDGF-C induces maturation of blood vessels in a model of glioblastoma and attenuates the response to anti-VEGF treatment. PLoS One. 2009;4(4):e5123. DOI: 10.1371/journal.pone.0005123</mixed-citation><mixed-citation xml:lang="ru">Di Tomaso E., London N., Fuja D. et al. PDGF-C induces maturation of blood vessels in a model of glioblastoma and attenuates the response to anti-VEGF treatment // PLoS One. 2009. Vol. 4, No. 4. P. e5123. DOI: 10.1371/journal.pone.0005123</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Guérit E, Arts F, Dachy G, et al. PDGF receptor mutations in human diseases. Cell Mol Life Sci. 2021;78(8):3867–3881. DOI: 10.1007/s00018-020-03753-y</mixed-citation><mixed-citation xml:lang="ru">Guérit E., Arts F., Dachy G. et al. PDGF receptor mutations in human diseases // Cell. Mol. Life Sci. 2021. Vol. 78, No. 8. P. 3867–3881. DOI: 10.1007/s00018-020-03753-y</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">Dico AL, Martelli C, Diceglie C, et al. Hypoxia-Inducible Factor-1α Activity as a switch for glioblastoma responsiveness to temozolomide. Front Oncol. 2018;8:249. DOI: 10.3389/fonc.2018.00249</mixed-citation><mixed-citation xml:lang="ru">Dico A.L., Martelli C., Diceglie C. et al. Hypoxia-inducible factor-1α activity as a switch for glioblastoma responsiveness to temozolomide // Front. Oncol. 2018. Vol. 8. P. 249. DOI: 10.3389/fonc.2018.00249</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">Renfrow JJ, Soike MH, West JL, et al. Attenuating hypoxia driven malignant behavior in glioblastoma with a novel hypoxia-inducible factor 2 alpha inhibitor. Sci Rep. 2020;10(1): 15195. DOI: 10.1038/s41598-020-72290-2</mixed-citation><mixed-citation xml:lang="ru">Renfrow J.J., Soike M.H., West J.L. et al. Attenuating hypoxia driven malignant behavior in glioblastoma with a novel hypoxia-inducible factor 2 alpha inhibitor // Sci. Rep. 2020. Vol. 10, No. 1. P. 15195. DOI: 10.1038/s41598-020-72290-2</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">Cornelison RC, Brennan CE, Kingsmore K., Munson JM. Convective forces increase CXCR4-dependent glioblastoma cell invasion in GL261 murine model. Sci Rep. 2018;8:17057. DOI: 10.1038/s41598-018-35141-9</mixed-citation><mixed-citation xml:lang="ru">Cornelison R.C., Brennan C.E., Kingsmore K.M., Munson J.M. Convective forces increase CXCR4-dependent glioblastoma cell invasion in GL261 murine model // Sci. Rep. 2018. Vol. 8. P. 17057. DOI: 10.1038/s41598-018-35141-9</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">Chao M, Liu N, Sun Z, et al. TGF-β signaling promotes glioma progression through stabilizing Sox9. Front Immunol. 2021;11:592080. DOI: 10.3389/fimmu.2020.592080</mixed-citation><mixed-citation xml:lang="ru">Chao M., Liu N., Sun Z. et al. TGF-β signaling promotes glioma progression through stabilizing Sox9 // Front. Immunol. 2021. Vol. 11. P. 592080. DOI: 10.3389/fimmu.2020.592080</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">Yang R, Li X, Wu Y, et al. EGFR activates GDH1 transcription to promote glutamine metabolism through MEK/ERK/ELK1 pathway in glioblastoma. Oncogene. 2020;39(14):2975–2986. DOI: 10.1038/s41388-020-1199-2</mixed-citation><mixed-citation xml:lang="ru">Yang R., Li X., Wu Y. et al. EGFR activates GDH1 transcription to promote glutamine metabolism through MEK/ERK/ELK1 pathway in glioblastoma // Oncogene. 2020. Vol. 39, No. 14. P. 2975–2986. DOI: 10.1038/s41388-020-1199-2</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">Pace KR, Dutt R, Galileo DS. Exosomal L1CAM stimulates glioblastoma cell motility, proliferation, and invasiveness. Int J Mol Sci. 2019;20(16):3982. DOI: 10.3390/ijms20163982</mixed-citation><mixed-citation xml:lang="ru">Pace K.R., Dutt R., Galileo D.S. Exosomal L1CAM stimulates glioblastoma cell motility, proliferation, and invasiveness // Int. J. Mol. Sci. 2019. Vol. 20, No. 16. P. 3982. DOI: 10.3390/ijms20163982</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">Lee Y, Lee JK, Ahn S, et al. WNT signaling in glioblastoma and therapeutic opportunities. Lab Invest. 2016;96(2):137–150. DOI: 10.1038/labinvest.2015.140</mixed-citation><mixed-citation xml:lang="ru">Lee Y., Lee JK., Ahn S. et al. WNT signaling in glioblastoma and therapeutic opportunities // Lab. Invest. 2016. Vol. 96, No. 2. P. 137–150. DOI: 10.1038/labinvest.2015.140</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">Cenciarelli C, Marei HE, Felsani A, et al. PDGFRα depletion attenuates glioblastoma stem cells features by modulation of STAT3, RB1 and multiple oncogenic signals. Oncotarget. 2016;7(33):53047–53063. DOI: 10.18632/oncotarget.10132</mixed-citation><mixed-citation xml:lang="ru">Cenciarelli C., Marei H.E., Felsani A. et al. PDGFRα depletion attenuates glioblastoma stem cells features by modulation of STAT3, RB1 and multiple oncogenic signals // Oncotarget. 2016. Vol. 7, No. 33. P. 53047–53063. DOI: 10.18632/oncotarget.10132</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">Gong Y, Ma Y, Sinyuk M, et al. Insulin-mediated signaling promotes proliferation and survival of glioblastoma through Akt activation. Neuro Oncol. 2016;18(1):48–57. DOI: 10.1093/neuonc/nov096</mixed-citation><mixed-citation xml:lang="ru">Gong Y., Ma Y., Sinyuk M. et al. Insulin-mediated signaling promotes proliferation and survival of glioblastoma through Akt activation // Neuro. Oncol. 2016. Vol. 18, No. 1. P. 48–57. DOI: 10.1093/neuonc/nov096</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">Oliva CR, Halloran B, Hjelmeland AB, et al. IGFBP6 controls the expansion of chemoresistant glioblastoma through paracrine IGF2/IGF-1R signaling. Cell Commun Signal. 2018;16(1):61. DOI: 10.1186/s12964-018-0273-7</mixed-citation><mixed-citation xml:lang="ru">Oliva C.R., Halloran B., Hjelmeland A.B. et al. IGFBP6 controls the expansion of chemoresistant glioblastoma through paracrine IGF2/IGF-1R signaling // Cell. Commun. Signal. 2018. Vol. 16, No. 1. P. 61. DOI: 10.1186/s12964-018-0273-7</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">Sesen J, Cammas A, Scotland SJ, et al. Int6/eIF3e is essential for proliferation and survival of human glioblastoma cells. Int J Mol Sci. 2014;15(2):2172–2190. DOI: 10.3390/ijms15022172</mixed-citation><mixed-citation xml:lang="ru">Sesen J., Cammas A., Scotland S.J. et al. Int6/eIF3e is essential for proliferation and survival of human glioblastoma cells // Int. J. Mol. Sci. 2014. Vol. 15, No. 2. P. 2172–2190. DOI: 10.3390/ijms15022172</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">Pan PC, Magge RS. Mechanisms of EGFR Resistance in Glioblastoma. Int J Mol Sci. 2020;21(22):8471. DOI: 10.3390/ijms21228471</mixed-citation><mixed-citation xml:lang="ru">Pan P.C., Magge R.S. Mechanisms of EGFR Resistance in Glioblastoma // Int. J. Mol. Sci. 2020. Vol. 21, No. 22. P. 8471. DOI: 10.3390/ijms21228471</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">Radin DP, Patel P. BDNF: an oncogene or tumor suppressor? Anticancer Res. 2017;37(8):3983–3990. DOI: 10.21873/anticanres.11783</mixed-citation><mixed-citation xml:lang="ru">Radin D.P., Patel P. BDNF: an oncogene or tumor suppressor? // Anticancer Res. 2017. Vol. 37, No. 8. P. 3983–3990. DOI: 10.21873/anticanres.11783</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">Nie E, Jin X, Miao F, et al. TGF-β1 modulates temozolomide resistance in glioblastoma via altered microRNA processing and elevated MGMT. Neuro Oncol. 2021;23(3):435–446. DOI: 10.1093/neuonc/noaa198</mixed-citation><mixed-citation xml:lang="ru">Nie E., Jin X., Miao F. et al. TGF-β1 modulates temozolomide resistance in glioblastoma via altered microRNA processing and elevated MGMT // Neuro. Oncol. 2021. Vol. 23, No. 3. P. 435–446. DOI: 10.1093/neuonc/noaa198</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">Bai Y, Lathia JD, Zhang P, et al. Molecular targeting of TRF2 suppresses the growth and tumorigenesis of glioblastoma stem cells. Glia. 2014;62(10):1687–1698. DOI: 10.1002/glia.22708</mixed-citation><mixed-citation xml:lang="ru">Bai Y., Lathia J.D., Zhang P. et al. Molecular targeting of TRF2 suppresses the growth and tumorigenesis of glioblastoma stem cells // Glia. 2014. Vol. 62, No. 10. P. 1687–1698. DOI: 10.1002/glia.22708</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang L-H, Yin A-A, Cheng J-X, et al. TRIM24 promotes glioma progression and enhances chemoresistance through activation of the PI3K/Akt signaling pathway. Oncogene. 2015;34(5):600–610. DOI: 10.1038/onc.2013.593</mixed-citation><mixed-citation xml:lang="ru">Zhang L.-H., Yin A.-A., Cheng J.-X. et al. TRIM24 promotes glioma progression and enhances chemoresistance through activation of the PI3K/Akt signaling pathway // Oncogene. 2015. Vol. 34, No. 5. P. 600–610. DOI: 10.1038/onc.2013.593</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">Yu Z, Chen Y, Wang S, et al. Inhibition of NF-κB results in anti-glioma activity and reduces temozolomide-induced chemoresistance by down-regulating MGMT gene expression. Cancer Lett. 2018;428:77–89. DOI: 10.1016/j.canlet.2018.04.033</mixed-citation><mixed-citation xml:lang="ru">Yu Z., Chen Y., Wang S. et al. Inhibition of NF-κB results in anti-glioma activity and reduces temozolomide-induced chemoresistance by down-regulating MGMT gene expression // Cancer Lett. 2018. Vol. 428. P. 77–89. DOI: 10.1016/j.canlet.2018.04.033</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">Edwards LA, Kim S, Madany M, et al. ZEB1 is a transcription factor that is prognostic and predictive in diffuse gliomas. Front Neurol. 2019;9:1199. DOI: 10.3389/fneur.2018.01199</mixed-citation><mixed-citation xml:lang="ru">Edwards L.A., Kim S., Madany M. et al. ZEB1 is a transcription factor that is prognostic and predictive in diffuse gliomas // Front. Neurol. 2019. Vol. 9. P. 1199. DOI: 10.3389/fneur.2018.01199</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">Xu K, Zhang Z, Pei H, et al. FoxO3a induces temozolomide resistance in glioblastoma cells via the regulation of β-catenin nuclear accumulation. Oncol Rep. 2017;37(4):2391–2397. DOI: 10.3892/or.2017.5459</mixed-citation><mixed-citation xml:lang="ru">Xu K., Zhang Z., Pei H. et al. FoxO3a induces temozolomide resistance in glioblastoma cells via the regulation of β-catenin nuclear accumulation // Oncol. Rep. 2017. Vol. 37, No. 4. P. 2391–2397. DOI: 10.3892/or.2017.5459</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang X, Lv QL, Huang YT, et al. Akt/FoxM1 signaling pathway-mediated upregulation of MYBL2 promotes progression of human glioma. J Exp Clin Cancer Res. 2017;36:105. DOI: 10.1186/s13046-017-0573-6</mixed-citation><mixed-citation xml:lang="ru">Zhang X., Lv QL., Huang Y.T. et al. Akt/FoxM1 signaling pathway-mediated upregulation of MYBL2 promotes progression of human glioma // J. Exp. Clin. Cancer Res. 2017. Vol. 36. P. 105. DOI: 10.1186/s13046-017-0573-6</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang C, Han X, Xu X, et al. FoxM1 drives ADAM17/EGFR activation loop to promote mesenchymal transition in glioblastoma. Cell Death Dis. 2018;9:469. DOI: 10.1038/s41419-018-0482-4</mixed-citation><mixed-citation xml:lang="ru">Zhang C., Han X., Xu X. et al. FoxM1 drives ADAM17/EGFR activation loop to promote mesenchymal transition in glioblastoma // Cell Death Dis. 2018. Vol. 9. P. 469. DOI: 10.1038/s41419-018-0482-4</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">Kim J-K, Jin X, Ham SW, et al. IRF7 promotes glioma cell invasion by inhibiting AGO2 expression. Tumor Biol. 2015;36(7):5561–5569. DOI: 10.1007/s13277-015-3226-4</mixed-citation><mixed-citation xml:lang="ru">Kim J.-K., Jin X., Ham S.W. et al. IRF7 promotes glioma cell invasion by inhibiting AGO2 expression // Tumor Biol. 2015. Vol. 36, No. 7. P. 5561–5569. DOI: 10.1007/s13277-015-3226-4</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">Agnihotri S, Wolf A, Munoz DM, et al. A GATA4-regulated tumor suppressor network represses formation of malignant human astrocytomas. J Exp Med. 2011;208(4):689–702. DOI: 10.1084/jem.20102099</mixed-citation><mixed-citation xml:lang="ru">Agnihotri S., Wolf A., Munoz D.M. et al. A GATA4-regulated tumor suppressor network represses formation of malignant human astrocytomas // J. Exp. Med. 2011. Vol. 208, No. 4. P. 689–702. DOI: 10.1084/jem.20102099</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">Wu Z, Wang L, Li G, et al. Increased expression of microRNA-9 predicts an unfavorable prognosis in human glioma. Mol Cell Biochem. 2013;384(1–2):263–268. DOI: 10.1007/s11010-013-1805-5</mixed-citation><mixed-citation xml:lang="ru">Wu Z., Wang L., Li G. et al. Increased expression of microRNA-9 predicts an unfavorable prognosis in human glioma // Mol. Cell. Biochem. 2013. Vol. 384, No. 1–2. P. 263–268. DOI: 10.1007/s11010-013-1805-5</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">Wang G, Wang JJ, Tang HM, et al. Targeting strategies on miRNA-21 and PDCD4 for glioblastoma. Arch Biochem Biophys. 2015;580:64–74. DOI: 10.1016/j.abb.2015.07.001</mixed-citation><mixed-citation xml:lang="ru">Wang G., Wang J.J., Tang H.M. et al. Targeting strategies on miRNA-21 and PDCD4 for glioblastoma // Arch. Biochem. Biophys. 2015. Vol. 580. P. 64–74. DOI: 10.1016/j.abb.2015.07.001</mixed-citation></citation-alternatives></ref><ref id="B65"><label>65.</label><citation-alternatives><mixed-citation xml:lang="en">Cheng Q, Ma X, Cao H, et al. Role of miR-223/paired box 6 signaling in temozolomide chemoresistance in glioblastoma multiforme cells. Mol Med Rep. 2017;15(2):597–604. DOI: 10.3892/mmr.2016.6078</mixed-citation><mixed-citation xml:lang="ru">Cheng Q., Ma X., Cao H. et al. Role of miR-223/paired box 6 signaling in temozolomide chemoresistance in glioblastoma multiforme cells // Mol. Med. Rep. 2017. Vol. 15, No. 2. P. 597–604. DOI: 10.3892/mmr.2016.6078</mixed-citation></citation-alternatives></ref><ref id="B66"><label>66.</label><citation-alternatives><mixed-citation xml:lang="en">Mathew LK, Skuli N, Mucaj V, et al. MiR-218 opposes a critical RTK-HIF pathway in mesenchymal glioblastoma. Proc Natl Acad Sci USA. 2014;111(1):291–296. DOI: 10.1073/pnas.1314341111</mixed-citation><mixed-citation xml:lang="ru">Mathew L.K., Skuli N., Mucaj V. et al. MiR-218 opposes a critical RTK-HIF pathway in mesenchymal glioblastoma // Proc. Natl. Acad. Sci. USA. 2014. Vol. 111, No. 1. P. 291–296. DOI: 10.1073/pnas.1314341111</mixed-citation></citation-alternatives></ref><ref id="B67"><label>67.</label><citation-alternatives><mixed-citation xml:lang="en">Wang Z, Li Z, Fu Y, et al. MiRNA-130a-3p inhibits cell proliferation, migration, and TMZ resistance in glioblastoma by targeting Sp1. Am J Transl Res. 2019;11(12):7272–7285.</mixed-citation><mixed-citation xml:lang="ru">Wang Z., Li Z., Fu Y. et al. MiRNA-130a-3p inhibits cell proliferation, migration, and TMZ resistance in glioblastoma by targeting Sp1 // Am. J. Transl. Res. 2019. Vol. 11, No. 12. P. 7272–7285.</mixed-citation></citation-alternatives></ref><ref id="B68"><label>68.</label><citation-alternatives><mixed-citation xml:lang="en">Gao Y-T, Chen X-B, Liu H-L. Up-regulation of miR-370-3p restores glioblastoma multiforme sensitivity to temozolomide by influencing MGMT expression. Sci Rep. 2016;6:32972. DOI: 10.1038/srep32972</mixed-citation><mixed-citation xml:lang="ru">Gao Y.-T., Chen X.-B., Liu H.-L. Up-regulation of miR-370-3p restores glioblastoma multiforme sensitivity to temozolomide by influencing MGMT expression // Sci. Rep. 2016. Vol. 6. P. 32972. DOI: 10.1038/srep32972</mixed-citation></citation-alternatives></ref><ref id="B69"><label>69.</label><citation-alternatives><mixed-citation xml:lang="en">Tian T, Mingyi M, Qiu X, et al. MicroRNA-101 reverses temozolomide resistance by inhibition of GSK3β in glioblastoma. Oncotarget. 2016;7(48):79584–79595. DOI: 10.18632/oncotarget.12861</mixed-citation><mixed-citation xml:lang="ru">Tian T., Mingyi M., Qiu X. et al. MicroRNA-101 reverses temozolomide resistance by inhibition of GSK3β in glioblastoma // Oncotarget. 2016. Vol. 7, No. 48. P. 79584–79595. DOI: 10.18632/oncotarget.12861</mixed-citation></citation-alternatives></ref><ref id="B70"><label>70.</label><citation-alternatives><mixed-citation xml:lang="en">Nie E, Jin X, Wu W, et al. MiR-198 enhances temozolomide sensitivity in glioblastoma by targeting MGMT. J Neurooncol. 2017;133(1):59–68. DOI: 10.1007/s11060-017-2425-9</mixed-citation><mixed-citation xml:lang="ru">Nie E., Jin X., Wu W. et al. MiR-198 enhances temozolomide sensitivity in glioblastoma by targeting MGMT // J. Neurooncol. 2017. Vol. 133, No. 1. P. 59–68. DOI: 10.1007/s11060-017-2425-9</mixed-citation></citation-alternatives></ref><ref id="B71"><label>71.</label><citation-alternatives><mixed-citation xml:lang="en">Wang G-H, Wang L-Y, Zhang C, et al. MiR-1225-5p acts as tumor suppressor in glioblastoma via targeting FNDC3B. Open Med (Wars). 2020;15(1):872–881. DOI: 10.1515/med-2020-0156</mixed-citation><mixed-citation xml:lang="ru">Wang G.-H., Wang L.-Y., Zhang C. et al. MiR-1225-5p acts as tumor suppressor in glioblastoma via targeting FNDC3B // Open Med. (Wars). 2020. Vol. 15, No. 1. P. 872–881. DOI: 10.1515/med-2020-0156</mixed-citation></citation-alternatives></ref><ref id="B72"><label>72.</label><citation-alternatives><mixed-citation xml:lang="en">Tanaka S, Kobayashi I, Oka H, et al. Drug-resistance gene expression and progression of astrocytic tumors. Brain Tumor Pathol. 2001;18(2):131–137. DOI: 10.1007/BF02479426</mixed-citation><mixed-citation xml:lang="ru">Tanaka S., Kobayashi I., Oka H. et al. Drug-resistance gene expression and progression of astrocytic tumors // Brain Tumor Pathol. 2001. Vol. 18, No. 2. P. 131–137. DOI: 10.1007/BF02479426</mixed-citation></citation-alternatives></ref><ref id="B73"><label>73.</label><citation-alternatives><mixed-citation xml:lang="en">Hegge B, Sjøttem E, Mikkola I. Generation of a PAX6 knockout glioblastoma cell line with changes in cell cycle distribution and sensitivity to oxidative stress. BMC Cancer. 2018;18(1):496. DOI: 10.1186/s12885-018-4394-6</mixed-citation><mixed-citation xml:lang="ru">Hegge B., Sjøttem E., Mikkola I. Generation of a PAX6 knockout glioblastoma cell line with changes in cell cycle distribution and sensitivity to oxidative stress // BMC Cancer. 2018. Vol. 18, No. 1. P. 496. DOI: 10.1186/s12885-018-4394-6</mixed-citation></citation-alternatives></ref><ref id="B74"><label>74.</label><citation-alternatives><mixed-citation xml:lang="en">Talamillo A, Grande L, Ruiz-Ontañon P, et al. ODZ1 allows glioblastoma to sustain invasiveness through a Myc-dependent transcriptional upregulation of RhoA. Oncogene. 2017;36(12):1733–1744. DOI: 10.1038/onc.2016.341</mixed-citation><mixed-citation xml:lang="ru">Talamillo A., Grande L., Ruiz-Ontañon P. et al. ODZ1 allows glioblastoma to sustain invasiveness through a Myc-dependent transcriptional upregulation of RhoA // Oncogene. 2017. Vol. 36, No. 12. P. 1733–1744. DOI: 10.1038/onc.2016.341</mixed-citation></citation-alternatives></ref><ref id="B75"><label>75.</label><citation-alternatives><mixed-citation xml:lang="en">Xia L, Huang Q, Nie D, et al. PAX3 is overexpressed in human glioblastomas and critically regulates the tumorigenicity of glioma cells. Brain Res. 2013;1521:68–78. DOI: 10.1016/j.brainres.2013.05.021</mixed-citation><mixed-citation xml:lang="ru">Xia L., Huang Q., Nie D. et al. PAX3 is overexpressed in human glioblastomas and critically regulates the tumorigenicity of glioma cells // Brain Res. 2013. Vol. 1521. P. 68–78. DOI: 10.1016/j.brainres.2013.05.021</mixed-citation></citation-alternatives></ref><ref id="B76"><label>76.</label><citation-alternatives><mixed-citation xml:lang="en">Pojo M, Gonçalves CS, Xavier-Magalhães A, et al. A transcriptomic signature mediated by HOXA9 promotes human glioblastoma initiation, aggressiveness and resistance to temozolomide. Oncotarget. 2015;6(10):7657–7674. DOI: 10.18632/oncotarget.3150</mixed-citation><mixed-citation xml:lang="ru">Pojo M., Gonçalves C.S., Xavier-Magalhães A. et al. A transcriptomic signature mediated by HOXA9 promotes human glioblastoma initiation, aggressiveness and resistance to temozolomide // Oncotarget. 2015. Vol. 6, No. 10. P. 7657–7674. DOI: 10.18632/oncotarget.3150</mixed-citation></citation-alternatives></ref><ref id="B77"><label>77.</label><citation-alternatives><mixed-citation xml:lang="en">Moiseeva NI, Susova OY, Mitrofanov AA, et al. Connection between proliferation rate and temozolomide sensitivity of primary glioblastoma cell culture and expression of YB-1 and LRP/MVP. Biochem (Mosc). 2016;81(6):628–635. DOI: 10.1134/S0006297916060109</mixed-citation><mixed-citation xml:lang="ru">Moiseeva N.I., Susova O.Y., Mitrofanov A.A. et al. Connection between proliferation rate and temozolomide sensitivity of primary glioblastoma cell culture and expression of YB-1 and LRP/MVP // Biochem. (Mosc). 2016. Vol. 81, No. 6. P. 628–635. DOI: 10.1134/S0006297916060109</mixed-citation></citation-alternatives></ref><ref id="B78"><label>78.</label><citation-alternatives><mixed-citation xml:lang="en">Cao Y, Li X, Kong S. et al. CDK4/6 inhibition suppresses tumour growth and enhances the effect of temozolomide in glioma cells. J Cell Mol Med. 2020;24(9):5135–5145. DOI: 10.1111/jcmm.15156</mixed-citation><mixed-citation xml:lang="ru">Cao Y., Li X., Kong S. et al. CDK4/6 inhibition suppresses tumour growth and enhances the effect of temozolomide in glioma cells // J. Cell Mol. Med. 2020. Vol. 24, No. 9. P. 5135–5145. DOI: 10.1111/jcmm.15156</mixed-citation></citation-alternatives></ref><ref id="B79"><label>79.</label><citation-alternatives><mixed-citation xml:lang="en">Farhad M, Rolig AS, Redmond WL. The role of Galectin-3 in modulating tumor growth and immunosuppression within the tumor microenvironment. Oncoimmunology. 2018;7(6):e1434467. DOI: 10.1080/2162402X.2018.1434467</mixed-citation><mixed-citation xml:lang="ru">Farhad M., Rolig A.S., Redmond W.L. The role of Galectin-3 in modulating tumor growth and immunosuppression within the tumor microenvironment // Oncoimmunology. 2018. Vol. 7, No. 6. P. e1434467. DOI: 10.1080/2162402X.2018.1434467</mixed-citation></citation-alternatives></ref><ref id="B80"><label>80.</label><citation-alternatives><mixed-citation xml:lang="en">Wang H, Song X, Huang Q, et al. LGALS3 promotes treatment resistance in glioblastoma and is associated with tumor risk and prognosis. Cancer Epidemiol Biomarkers Prev. 2019;28(4):760–769. DOI: 10.1158/1055-9965.EPI-18-0638</mixed-citation><mixed-citation xml:lang="ru">Wang H., Song X., Huang Q. et al. LGALS3 promotes treatment resistance in glioblastoma and is associated with tumor risk and prognosis // Cancer Epidemiol. Biomarkers Prev. 2019. Vol. 28, No. 4. P. 760–769. DOI: 10.1158/1055-9965.EPI-18-0638</mixed-citation></citation-alternatives></ref><ref id="B81"><label>81.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang M, Zhao Y, Zhao J, et al. Impact of AKAP6 polymorphisms on Glioma susceptibility and prognosis. BMC Neurol. 2019;19:296. DOI: 10.1186/s12883-019-1504-2</mixed-citation><mixed-citation xml:lang="ru">Zhang M., Zhao Y., Zhao J. et al. Impact of AKAP6 polymorphisms on Glioma susceptibility and prognosis // BMC Neurol. 2019. Vol. 19. P. 296. DOI: 10.1186/s12883-019-1504-2</mixed-citation></citation-alternatives></ref><ref id="B82"><label>82.</label><citation-alternatives><mixed-citation xml:lang="en">Mellai M, Cattaneo M, Storaci AM, et al. SEL1L SNP rs12435998, a predictor of glioblastoma survival and response to radio-chemotherapy. Oncotarget. 2015;6(14):12452–12467. DOI: 10.18632/oncotarget.3611</mixed-citation><mixed-citation xml:lang="ru">Mellai M., Cattaneo M., Storaci A.M. et al. SEL1L SNP rs12435998, a predictor of glioblastoma survival and response to radio-chemotherapy // Oncotarget. 2015. Vol. 6, No. 14. P. 12452–12467. DOI: 10.18632/oncotarget.3611</mixed-citation></citation-alternatives></ref><ref id="B83"><label>83.</label><citation-alternatives><mixed-citation xml:lang="en">Riboni L, Hadi LA, Navone SE, et al. Sphingosine-1-phosphate in the tumor microenvironment: a signaling hub regulating cancer hallmarks. Cells. 2020;9(2):337. DOI: 10.3390/cells9020337</mixed-citation><mixed-citation xml:lang="ru">Riboni L., Hadi L.A., Navone S.E. et al. Sphingosine-1-phosphate in the tumor microenvironment: a signaling hub regulating cancer hallmarks // Cells. 2020. Vol. 9, No. 2. P. 337. DOI: 10.3390/cells9020337</mixed-citation></citation-alternatives></ref><ref id="B84"><label>84.</label><citation-alternatives><mixed-citation xml:lang="en">Chen D. Tumor formation and drug resistance properties of human glioblastoma side population cells. Mol Med Rep. 2015;11(6):4309–4314. DOI: 10.3892/mmr.2015.3279</mixed-citation><mixed-citation xml:lang="ru">Chen D. Tumor formation and drug resistance properties of human glioblastoma side population cells // Mol. Med. Rep. 2015. Vol. 11, No. 6. P. 4309–4314. DOI: 10.3892/mmr.2015.3279</mixed-citation></citation-alternatives></ref><ref id="B85"><label>85.</label><citation-alternatives><mixed-citation xml:lang="en">Kaneko S, Nakatani Y, Takezaki T, et al. Ceacam1L modulates STAT3 signaling to control the proliferation of glioblastoma-initiating cells. Cancer Res. 2015;75(19):4224–4234. DOI: 10.3892/mmr.2015.3279</mixed-citation><mixed-citation xml:lang="ru">Kaneko S., Nakatani Y., Takezaki T. et al. Ceacam1L modulates STAT3 signaling to control the proliferation of glioblastoma-initiating cells // Cancer Res. 2015. Vol. 75, No. 19. P. 4224–4234. DOI: 10.3892/mmr.2015.3279</mixed-citation></citation-alternatives></ref><ref id="B86"><label>86.</label><citation-alternatives><mixed-citation xml:lang="en">Yu F, Li G, Gao J, et al. SPOCK1 is upregulated in recurrent glioblastoma and contributes to metastasis and temozolomide resistance. Cell Prolif. 2016;49(2):195–206. DOI: 10.1111/cpr.12241</mixed-citation><mixed-citation xml:lang="ru">Yu F., Li G., Gao J. et al. SPOCK1 is upregulated in recurrent glioblastoma and contributes to metastasis and temozolomide resistance // Cell Prolif. 2016. Vol. 49, No. 2. P. 195–206. DOI: 10.1111/cpr.12241</mixed-citation></citation-alternatives></ref><ref id="B87"><label>87.</label><citation-alternatives><mixed-citation xml:lang="en">Afghani N, Mehta T, Wang J, et al. Microtubule actin cross-linking factor 1, a novel target in glioblastoma. Int J Oncol. 2017;50(1):310–316. DOI: 10.3892/ijo.2016.3798</mixed-citation><mixed-citation xml:lang="ru">Afghani N., Mehta T., Wang J. et al. Microtubule actin cross-linking factor 1, a novel target in glioblastoma // Int. J. Oncol. 2017. Vol. 50, No. 1. P. 310–316. DOI: 10.3892/ijo.2016.3798</mixed-citation></citation-alternatives></ref><ref id="B88"><label>88.</label><citation-alternatives><mixed-citation xml:lang="en">Guerrero PA, Yin W, Camacho L, et al. Oncogenic role of Merlin/NF2 in glioblastoma. Oncogene. 2015;34(20):2621–2630. DOI: 10.1038/onc.2014.185</mixed-citation><mixed-citation xml:lang="ru">Guerrero P.A., Yin W., Camacho L. et al. Oncogenic role of Merlin/NF2 in glioblastoma // Oncogene. 2015. Vol. 34, No. 20. P. 2621–2630. DOI: 10.1038/onc.2014.185</mixed-citation></citation-alternatives></ref><ref id="B89"><label>89.</label><citation-alternatives><mixed-citation xml:lang="en">Xie Z, Janczyk PŁ, Zhang Y, et al. A cytoskeleton regulator AVIL drives tumorigenesis in glioblastoma. Nat Commun. 2020;11:3457. DOI: 10.1038/s41467-020-17279-1</mixed-citation><mixed-citation xml:lang="ru">Xie Z., Janczyk P.Ł., Zhang Y. et al. A cytoskeleton regulator AVIL drives tumorigenesis in glioblastoma // Nat. Commun. 2020. Vol. 11. P. 3457. DOI: 10.1038/s41467-020-17279-1</mixed-citation></citation-alternatives></ref><ref id="B90"><label>90.</label><citation-alternatives><mixed-citation xml:lang="en">Noh H, Yan J, Hong S, et al. Discovery of cell surface vimentin targeting mAb for direct disruption of GBM tumor initiating cells. Oncotarget. 2016;7(44):72021–72032. DOI: 10.18632/oncotarget.12458</mixed-citation><mixed-citation xml:lang="ru">Noh H., Yan J., Hong S. et al. Discovery of cell surface vimentin targeting mAb for direct disruption of GBM tumor initiating cells // Oncotarget. 2016. Vol. 7, No. 44. P. 72021–72032. DOI: 10.18632/oncotarget.12458</mixed-citation></citation-alternatives></ref><ref id="B91"><label>91.</label><citation-alternatives><mixed-citation xml:lang="en">Zhao J, Zhang L, Dong X, et al. High expression of vimentin is associated with progression and a poor outcome in glioblastoma. Appl Immunohistochem Mol Morphol. 2018;26(5):337–344. DOI: 10.1097/PAI.0000000000000420</mixed-citation><mixed-citation xml:lang="ru">Zhao J., Zhang L., Dong X. et al. High expression of vimentin is associated with progression and a poor outcome in glioblastoma // Appl. Immunohistochem. Mol. Morphol. 2018. Vol. 26, No. 5. P. 337–344. DOI: 10.1097/PAI.0000000000000420</mixed-citation></citation-alternatives></ref><ref id="B92"><label>92.</label><citation-alternatives><mixed-citation xml:lang="en">Satelli A, Li S. Vimentin in cancer and its potential as a molecular target for cancer therapy. Cell Mol Life Sci. 2011;68(18):3033–3046. DOI: 10.1007/s00018-011-0735-1</mixed-citation><mixed-citation xml:lang="ru">Satelli A., Li S. Vimentin in cancer and its potential as a molecular target for cancer therapy// Cell. Mol. Life Sci. 2011. Vol. 68, No. 18. P. 3033–3046. DOI: 10.1007/s00018-011-0735-1</mixed-citation></citation-alternatives></ref><ref id="B93"><label>93.</label><citation-alternatives><mixed-citation xml:lang="en">Zottel A, Jovčevska I, Šamec N, Komel R. Cytoskeletal proteins as glioblastoma biomarkers and targets for therapy: A systematic review. Crit Rev Oncol Hematol. 2021;160:103283. DOI: 10.1016/j.critrevonc.2021.103283</mixed-citation><mixed-citation xml:lang="ru">Zottel A., Jovčevska I., Šamec N., Komel R. Cytoskeletal proteins as glioblastoma biomarkers and targets for therapy: A systematic review // Crit. Rev. Oncol. Hematol. 2021. Vol. 160. P. 103283. DOI: 10.1016/j.critrevonc.2021.103283</mixed-citation></citation-alternatives></ref><ref id="B94"><label>94.</label><citation-alternatives><mixed-citation xml:lang="en">Ahir BK, Engelhard HH, Lakka SS. Tumor development and angiogenesis in adult brain tumor: glioblastoma. Mol Neurobiol. 2020;57:2461–2478. DOI: 10.1007/s12035-020-01892-8</mixed-citation><mixed-citation xml:lang="ru">Ahir B.K., Engelhard H.H., Lakka S.S. Tumor development and angiogenesis in adult brain tumor: glioblastoma // Mol. Neurobiol. 2020. Vol. 57. P. 2461–2478. DOI: 10.1007/s12035-020-01892-8</mixed-citation></citation-alternatives></ref><ref id="B95"><label>95.</label><citation-alternatives><mixed-citation xml:lang="en">Carmeliet P, Jain RK. Principles and mechanisms of vessel normalization for cancer and other angiogenic diseases. Nat Rev Drug Discov. 2011;10(6):417–427. DOI: 10.1038/nrd3455</mixed-citation><mixed-citation xml:lang="ru">Carmeliet P., Jain R.K. Principles and mechanisms of vessel normalization for cancer and other angiogenic diseases // Nat. Rev. Drug Discov. 2011. Vol. 10, No. 6. P. 417–427. DOI: 10.1038/nrd3455</mixed-citation></citation-alternatives></ref><ref id="B96"><label>96.</label><citation-alternatives><mixed-citation xml:lang="en">Loureiro LVM, Neder L, Callegaro-Filho D, et al. The immunohistochemical landscape of the VEGF family and its receptors in glioblastomas. Surg Exp Pathol. 2020;3:9. DOI: 10.1186/s42047-020-00060-5</mixed-citation><mixed-citation xml:lang="ru">Loureiro L.V.M., Neder L., Callegaro-Filho D. et al. The immunohistochemical landscape of the VEGF family and its receptors in glioblastomas // Surg. Exp. Pathol. 2020. Vol. 3. P. 9. DOI: 10.1186/s42047-020-00060-5</mixed-citation></citation-alternatives></ref><ref id="B97"><label>97.</label><citation-alternatives><mixed-citation xml:lang="en">Arif SH, Pandith AA, Tabasum R, et al. Significant effect of anti-tyrosine Kinase Inhibitor (Gefitinib) on overall survival of the glioblastoma multiforme patients in the backdrop of mutational status of epidermal growth factor receptor and PTEN Genes. Asian J Neurosurg. 2018;13(1):46–52. DOI: 10.4103/ajns.AJNS_95_17</mixed-citation><mixed-citation xml:lang="ru">Arif S.H., Pandith A.A., Tabasum R. et al. Significant effect of anti-tyrosine Kinase Inhibitor (Gefitinib) on overall survival of the glioblastoma multiforme patients in the backdrop of mutational status of epidermal growth factor receptor and PTEN Genes // Asian J. Neurosurg. 2018. Vol. 13, No. 1. P. 46–52. DOI: 10.4103/ajns.AJNS_95_17</mixed-citation></citation-alternatives></ref><ref id="B98"><label>98.</label><citation-alternatives><mixed-citation xml:lang="en">Krishnan S, Szabo E, Burghardt I, et al. Modulation of cerebral endothelial cell function by TGF-β in glioblastoma: VEGF-dependent angiogenesis versus endothelial mesenchymal transition. Oncotarget. 2015;6(26):22480–22495. DOI: 10.18632/oncotarget.4310</mixed-citation><mixed-citation xml:lang="ru">Krishnan S., Szabo E., Burghardt I. et al. Modulation of cerebral endothelial cell function by TGF-β in glioblastoma: VEGF-dependent angiogenesis versus endothelial mesenchymal transition // Oncotarget. 2015. Vol. 6, No. 26. P. 22480–22495. DOI: 10.18632/oncotarget.4310</mixed-citation></citation-alternatives></ref><ref id="B99"><label>99.</label><citation-alternatives><mixed-citation xml:lang="en">Ichikawa K, Watanabe Miyano S, Minoshima Y, et al. Activated FGF2 signaling pathway in tumor vasculature is essential for acquired resistance to anti-VEGF therapy. Sci Rep. 2020;10:2939. DOI: 10.1038/s41598-020-59853-z</mixed-citation><mixed-citation xml:lang="ru">Ichikawa K., Watanabe Miyano S., Minoshima Y. et al. Activated FGF2 signaling pathway in tumor vasculature is essential for acquired resistance to anti-VEGF therapy // Sci. Rep. 2020. Vol. 10. P. 2939. DOI: 10.1038/s41598-020-59853-z</mixed-citation></citation-alternatives></ref><ref id="B100"><label>100.</label><citation-alternatives><mixed-citation xml:lang="en">Goldman CK, Kim J, Wong WL, et al. Epidermal growth factor stimulates vascular endothelial growth factor production by human malignant glioma cells: a model of glioblastoma multiforme pathophysiology. Mol Biol Cell. 1993;4(1):121–133. DOI: 10.1091/mbc.4.1.121</mixed-citation><mixed-citation xml:lang="ru">Goldman C.K., Kim J., Wong W.L. et al. Epidermal growth factor stimulates vascular endothelial growth factor production by human malignant glioma cells: a model of glioblastoma multiforme pathophysiology // Mol. Biol. Cell. 1993. Vol. 4, No. 1. P. 121–133. DOI: 10.1091/mbc.4.1.121</mixed-citation></citation-alternatives></ref><ref id="B101"><label>101.</label><citation-alternatives><mixed-citation xml:lang="en">Krishnan S, Szabo E, Burghardt I, et al. Modulation of cerebral endothelial cell function by TGF-β in glioblastoma: VEGF-dependent angiogenesis versus endothelial mesenchymal transition. Oncotarget. 2015. Vol. 6, No. 26. P. 22480–22495. DOI: 10.18632/oncotarget.4310</mixed-citation><mixed-citation xml:lang="ru">Krishnan S., Szabo E., Burghardt I. et al. Modulation of cerebral endothelial cell function by TGF-β in glioblastoma: VEGF-dependent angiogenesis versus endothelial mesenchymal transition // Oncotarget. 2015. Vol. 6, No. 26. P. 22480–22495. DOI: 10.18632/oncotarget.4310</mixed-citation></citation-alternatives></ref><ref id="B102"><label>102.</label><citation-alternatives><mixed-citation xml:lang="en">Kessler T, Sahm F, Blaes J, et al. Glioma cell VEGFR-2 confers resistance to chemotherapeutic and antiangiogenic treatments in PTEN-deficient glioblastoma. Oncotarget. 2015;6(31):31050–31068. DOI: 10.18632/oncotarget.2910</mixed-citation><mixed-citation xml:lang="ru">Kessler T., Sahm F., Blaes J. et al. Glioma cell VEGFR-2 confers resistance to chemotherapeutic and antiangiogenic treatments in PTEN-deficient glioblastoma // Oncotarget. 2015. Vol. 6, No. 31. P. 31050–31068. DOI: 10.18632/oncotarget.2910</mixed-citation></citation-alternatives></ref><ref id="B103"><label>103.</label><citation-alternatives><mixed-citation xml:lang="en">Serban F, Daianu O, Tataranu LG, et al. Silencing of epidermal growth factor, latrophilin and seven transmembrane domain-containing protein 1 (ELTD1) via siRNA-induced cell death in glioblastoma. J Immunoassay Immunochem. 2017;38(1):21–33. DOI: 10.1080/15321819.2016.1209217</mixed-citation><mixed-citation xml:lang="ru">Serban F., Daianu O., Tataranu L.G. et al. Silencing of epidermal growth factor, latrophilin and seven transmembrane domain-containing protein 1 (ELTD1) via siRNA-induced cell death in glioblastoma // J. Immunoassay Immunochem. 2017. Vol. 38, No. 1. P. 21–33. DOI: 10.1080/15321819.2016.1209217</mixed-citation></citation-alternatives></ref><ref id="B104"><label>104.</label><citation-alternatives><mixed-citation xml:lang="en">Yuan G, Yan S, Xue H, et al. JSI-124 suppresses invasion and angiogenesis of glioblastoma cells in vitro. PLoS One. 2015;10(3):e0118894. DOI: 10.1371/journal.pone.0118894</mixed-citation><mixed-citation xml:lang="ru">Yuan G., Yan S., Xue H. et al. JSI-124 suppresses invasion and angiogenesis of glioblastoma cells in vitro // PLoS One. 2015. Vol. 10, No. 3. P. e0118894. DOI: 10.1371/journal.pone.0118894</mixed-citation></citation-alternatives></ref><ref id="B105"><label>105.</label><citation-alternatives><mixed-citation xml:lang="en">Chang N, Ahn SH, Kong DS, et al. The role of STAT3 in glioblastoma progression through dual influences on tumor cells and the immune microenvironment. Mol Cell Endocrinol. 2017;451:53–65. DOI: 10.1016/j.mce.2017.01.004</mixed-citation><mixed-citation xml:lang="ru">Chang N., Ahn S.H., Kong D.S. et al. The role of STAT3 in glioblastoma progression through dual influences on tumor cells and the immune microenvironment // Mol. Cell. Endocrinol. 2017. Vol. 451. P. 53–65. DOI: 10.1016/j.mce.2017.01.004</mixed-citation></citation-alternatives></ref><ref id="B106"><label>106.</label><citation-alternatives><mixed-citation xml:lang="en">Li JL, Sainson RC, Oon CE, et al. DLL4-Notch signaling mediates tumor resistance to anti-VEGF therapy in vivo. Cancer Res. 2011;71(18):6073–6083. DOI: 10.1158/0008-5472.CAN-11-1704</mixed-citation><mixed-citation xml:lang="ru">Li J.L., Sainson R.C., Oon C.E. et al. DLL4-Notch signaling mediates tumor resistance to anti-VEGF therapy in vivo // Cancer Res. 2011. Vol. 71, No. 18. P. 6073–6083. DOI: 10.1158/0008-5472.CAN-11-1704</mixed-citation></citation-alternatives></ref><ref id="B107"><label>107.</label><citation-alternatives><mixed-citation xml:lang="en">Hochart A, Leblond P, Le Bourhis X, et al. MET receptor inhibition: Hope against resistance to targeted therapies? Bull Cancer. 2017;104(2):157–166. (In French). DOI: 10.1016/j.bulcan.2016.10.014</mixed-citation><mixed-citation xml:lang="ru">Hochart A., Leblond P., Le Bourhis X. et al. MET receptor inhibition: Hope against resistance to targeted therapies? // Bull. Cancer. 2017. Vol. 104, No. 2. P. 157–166. (In French). DOI: 10.1016/j.bulcan.2016.10.014</mixed-citation></citation-alternatives></ref><ref id="B108"><label>108.</label><citation-alternatives><mixed-citation xml:lang="en">Chen L, Feng P, Li S, et al. Effect of hypoxia-inducible factor-1α silencing on the sensitivity of human brain glioma cells to doxorubicin and etoposide. Neurochem Res. 2009;34(5):984–990. DOI: 10.1007/s11064-008-9864-9</mixed-citation><mixed-citation xml:lang="ru">Chen L., Feng P., Li S. et al. Effect of hypoxia-inducible factor-1α silencing on the sensitivity of human brain glioma cells to doxorubicin and etoposide // Neurochem. Res. 2009. Vol. 34, No. 5. P. 984–990. DOI: 10.1007/s11064-008-9864-9</mixed-citation></citation-alternatives></ref><ref id="B109"><label>109.</label><citation-alternatives><mixed-citation xml:lang="en">Muh CR, Joshi S, Singh AR, et al. PTEN status mediates 2ME2 anti-tumor efficacy in preclinical glioblastoma models: role of HIF1α suppression. J Neurooncol. 2014;116(1):89–97. DOI: 10.1007/s11060-013-1283-3</mixed-citation><mixed-citation xml:lang="ru">Muh C.R., Joshi S., Singh A.R. et al. PTEN status mediates 2ME2 anti-tumor efficacy in preclinical glioblastoma models: role of HIF1α suppression // J. Neurooncol. 2014. Vol. 116, No. 1. P. 89–97. DOI: 10.1007/s11060-013-1283-3</mixed-citation></citation-alternatives></ref><ref id="B110"><label>110.</label><citation-alternatives><mixed-citation xml:lang="en">Jimenez-Pascual A, Siebzehnrubl FA. Fibroblast growth factor receptor functions in glioblastoma. Cells. 2019;8(7):715. DOI: 10.3390/cells8070715</mixed-citation><mixed-citation xml:lang="ru">Jimenez-Pascual A., Siebzehnrubl F.A. Fibroblast growth factor receptor functions in glioblastoma // Cells. 2019. Vol. 8, No. 7. P. 715. DOI: 10.3390/cells8070715</mixed-citation></citation-alternatives></ref><ref id="B111"><label>111.</label><citation-alternatives><mixed-citation xml:lang="en">Hierro C, Rodon J, Tabernero J. Fibroblast growth factor (FGF) receptor/FGF inhibitors: novel targets and strategies for optimization of response of solid tumors. Semin Oncol. 2015;42(6):801–819. DOI: 10.1053/j.seminoncol.2015.09.027</mixed-citation><mixed-citation xml:lang="ru">Hierro C., Rodon J., Tabernero J. Fibroblast growth factor (FGF) receptor/FGF inhibitors: novel targets and strategies for optimization of response of solid tumors // Semin. Oncol. 2015. Vol. 42, No. 6. P. 801–819. DOI: 10.1053/j.seminoncol.2015.09.027</mixed-citation></citation-alternatives></ref><ref id="B112"><label>112.</label><citation-alternatives><mixed-citation xml:lang="en">Hsieh A, Ellsworth R, Hsieh D. Hedgehog/GLI1 regulates IGF dependent malignant behaviors in glioma stem cells. J Cell Physiol. 2011;226(4):1118–1127. DOI: 10.1002/jcp.22433</mixed-citation><mixed-citation xml:lang="ru">Hsieh A., Ellsworth R., Hsieh D. Hedgehog/GLI1 regulates IGF dependent malignant behaviors in glioma stem cells // J. Cell. Physiol. 2011. Vol. 226, No. 4. P. 1118–1127. DOI: 10.1002/jcp.22433</mixed-citation></citation-alternatives></ref><ref id="B113"><label>113.</label><citation-alternatives><mixed-citation xml:lang="en">Cherepanov SA, Baklaushev VP, Gabashvili AN, et al. Hedgehog signaling in the pathogenesis of neuro-oncology diseases. Biomed. Khim. 2015;61(3):332–342. (In Russ.). DOI: 10.18097/PBMC20156103332</mixed-citation><mixed-citation xml:lang="ru">Cherepanov S.A., Baklaushev V.P., Gabashvili A.N. et al. Hedgehog signaling in the pathogenesis of neuro-oncology diseases // Biomed. Khim. 2015. Vol. 61, No. 3. P. 332–342. (In Russ.). DOI: 10.18097/PBMC20156103332</mixed-citation></citation-alternatives></ref><ref id="B114"><label>114.</label><citation-alternatives><mixed-citation xml:lang="en">Tirrò E, Massimino M, Romano C, et al. Prognostic and therapeutic roles of the insulin growth factor system in glioblastoma. Front Oncol. 2021;10:612385. DOI: 10.3389/fonc.2020.612385</mixed-citation><mixed-citation xml:lang="ru">Tirrò E., Massimino M., Romano C. et al. Prognostic and therapeutic roles of the insulin growth factor system in glioblastoma // Front. Oncol. 2021. Vol. 10. P. 612385. DOI: 10.3389/fonc.2020.612385</mixed-citation></citation-alternatives></ref><ref id="B115"><label>115.</label><citation-alternatives><mixed-citation xml:lang="en">Martin V, Xu J, Pabbisetty SK, et al. Tie2-mediated multidrug resistance in malignant gliomas is associated with upregulation of ABC transporters. Oncogene. 2009;28(24):2358–2363. DOI: 10.1038/onc.2009.103</mixed-citation><mixed-citation xml:lang="ru">Martin V., Xu J., Pabbisetty S.K. et al. Tie2-mediated multidrug resistance in malignant gliomas is associated with upregulation of ABC transporters // Oncogene. 2009. Vol. 28, No. 24. P. 2358–2363. DOI: 10.1038/onc.2009.103</mixed-citation></citation-alternatives></ref><ref id="B116"><label>116.</label><citation-alternatives><mixed-citation xml:lang="en">di Tomaso E, Snuderl M, Kamoun WS, et al. Glioblastoma recurrence after cediranib therapy in patients: lack of “rebound” revascularization as mode of escape. Cancer Res. 2011;71(1):19–28. DOI: 10.1158/0008-5472.CAN-10-2602</mixed-citation><mixed-citation xml:lang="ru">Di Tomaso E., Snuderl M., Kamoun W.S. et al. Glioblastoma recurrence after cediranib therapy in patients: lack of “rebound” revascularization as mode of escape // Cancer Res. 2011. Vol. 71, No. 1. P. 19–28. DOI: 10.1158/0008-5472.CAN-10-2602</mixed-citation></citation-alternatives></ref><ref id="B117"><label>117.</label><citation-alternatives><mixed-citation xml:lang="en">Ma Y, Yuan R-Q, Fan S, et al. Identification of genes that modulate sensitivity of U373MG glioblastoma cells to cis-platinum. Anticancer Drugs. 2006;17(7):733–751. DOI: 10.1097/01.cad.0000217429.67455.18</mixed-citation><mixed-citation xml:lang="ru">Ma Y., Yuan R.-Q., Fan S. et al. Identification of genes that modulate sensitivity of U373MG glioblastoma cells to cis-platinum // Anticancer Drugs. 2006. Vol. 17, No. 7. P. 733–751. DOI: 10.1097/01.cad.0000217429.67455.18</mixed-citation></citation-alternatives></ref><ref id="B118"><label>118.</label><citation-alternatives><mixed-citation xml:lang="en">Yadav VN, Zamler D, Baker GJ, et al. CXCR4 increases in-vivo glioma perivascular invasion, and reduces radiation induced apoptosis: A genetic knockdown study. Oncotarget. 2016;7:83701–83719. DOI: 10.18632/oncotarget.13295</mixed-citation><mixed-citation xml:lang="ru">Yadav V.N., Zamler D., Baker G.J. et al. CXCR4 increases in-vivo glioma perivascular invasion, and reduces radiation induced apoptosis: A genetic knockdown study // Oncotarget. 2016. Vol. 7. P. 83701–83719. DOI: 10.18632/oncotarget.13295</mixed-citation></citation-alternatives></ref><ref id="B119"><label>119.</label><citation-alternatives><mixed-citation xml:lang="en">Gatti M, Pattarozzi A, Bajetto A, et al. Inhibition of CXCL12/CXCR4 autocrine/paracrine loop reduces viability of human glioblastoma stem-like cells affecting self-renewal activity. Toxicology. 2013;314(2-3):209–220. DOI: 10.1016/j.tox.2013.10.003</mixed-citation><mixed-citation xml:lang="ru">Gatti M., Pattarozzi A., Bajetto A. et al. Inhibition of CXCL12/CXCR4 autocrine/paracrine loop reduces viability of human glioblastoma stem-like cells affecting self-renewal activity // Toxicology. 2013. Vol. 314, No. 2–3. P. 209–220. DOI: 10.1016/j.tox.2013.10.003</mixed-citation></citation-alternatives></ref><ref id="B120"><label>120.</label><citation-alternatives><mixed-citation xml:lang="en">Yin D, Chen W, O’Kelly J, et al. Connective tissue growth factor associated with oncogenic activities and drug resistance in glioblastoma multiforme. Int J Cancer. 2010;127(10):2257–2267. DOI: 10.1002/ijc.25257</mixed-citation><mixed-citation xml:lang="ru">Yin D., Chen W., O’Kelly J. et al. Connective tissue growth factor associated with oncogenic activities and drug resistance in glioblastoma multiforme // Int. J. Cancer. 2010. Vol. 127, No. 10. P. 2257–2267. DOI: 10.1002/ijc.25257</mixed-citation></citation-alternatives></ref><ref id="B121"><label>121.</label><citation-alternatives><mixed-citation xml:lang="en">Dai D, Huang W, Lu Q, et al. miR-24 regulates angiogenesis in gliomas. Mol Med Rep. 2018;18(1):358–368. DOI: 10.3892/mmr.2018.8978</mixed-citation><mixed-citation xml:lang="ru">Dai D., Huang W., Lu Q. et al. miR-24 regulates angiogenesis in gliomas // Mol. Med. Rep. 2018. Vol. 18, No. 1. P. 358–368. DOI: 10.3892/mmr.2018.8978</mixed-citation></citation-alternatives></ref><ref id="B122"><label>122.</label><citation-alternatives><mixed-citation xml:lang="en">Smits M, Wurdinger T, van het Hof B, et al. Myc-associated zinc finger protein (MAZ) is regulated by miR-125b and mediates VEGF-induced angiogenesis in glioblastoma. FASEB J. 2012;26(6):2639–2647. DOI: 10.1096/fj.11-202820</mixed-citation><mixed-citation xml:lang="ru">Smits M., Wurdinger T., van het Hof B. et al. Myc-associated zinc finger protein (MAZ) is regulated by miR-125b and mediates VEGF-induced angiogenesis in glioblastoma // FASEB J. 2012. Vol. 26, No. 6. P. 2639–2647. DOI: 10.1096/fj.11-202820</mixed-citation></citation-alternatives></ref><ref id="B123"><label>123.</label><citation-alternatives><mixed-citation xml:lang="en">Wang Q, Xu B, Du J, et al. MicroRNA-139-5p/Flt1/Wnt/β-catenin regulatory crosstalk modulates the progression of glioma. Int J Mol Med. 2018;41(4):2139–2149. DOI: 10.3892/ijmm.2018.3439</mixed-citation><mixed-citation xml:lang="ru">Wang Q., Xu B., Du J. et al. MicroRNA-139-5p/Flt1/Wnt/β-catenin regulatory crosstalk modulates the progression of glioma // Int. J. Mol. Med. 2018. Vol. 41, No. 4. P. 2139–2149. DOI: 10.3892/ijmm.2018.3439</mixed-citation></citation-alternatives></ref><ref id="B124"><label>124.</label><citation-alternatives><mixed-citation xml:lang="en">Duncan CG, Killela PJ, Payne CA, et al. Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genes. Oncotarget. 2010;1(4):265–277. DOI: 10.18632/oncotarget.137</mixed-citation><mixed-citation xml:lang="ru">Duncan C.G., Killela P.J., Payne C.A. et al. Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genes // Oncotarget. 2010. Vol. 1, No. 4. P. 265–277. DOI: 10.18632/oncotarget.137</mixed-citation></citation-alternatives></ref><ref id="B125"><label>125.</label><citation-alternatives><mixed-citation xml:lang="en">Wang L, Shi Z-M, Jiang C-F, et al. MiR-143 acts as a tumor suppressor by targeting N-RAS and enhances temozolomide-induced apoptosis in glioma. Oncotarget. 2014;5:5416. DOI: 10.18632/oncotarget.2116</mixed-citation><mixed-citation xml:lang="ru">Wang L., Shi Z.-M., Jiang C.-F. et al. MiR-143 acts as a tumor suppressor by targeting N-RAS and enhances temozolomide-induced apoptosis in glioma // Oncotarget. 2014. Vol. 5. P. 5416. DOI: 10.18632/oncotarget.2116</mixed-citation></citation-alternatives></ref><ref id="B126"><label>126.</label><citation-alternatives><mixed-citation xml:lang="en">Chen K-C, Chen P-H, Ho K-H, et al. IGF-1-enhanced miR-513a-5p signaling desensitizes glioma cells to temozolomide by targeting the NEDD4L-inhibited Wnt/β-catenin pathway. PLoS One. 2019;14(12):e0225913. DOI: 10.1371/journal.pone.0225913</mixed-citation><mixed-citation xml:lang="ru">Chen K.-C., Chen P.-H., Ho K.-H. et al. IGF-1-enhanced miR-513a-5p signaling desensitizes glioma cells to temozolomide by targeting the NEDD4L-inhibited Wnt/β-catenin pathway // PLoS One. 2019. Vol. 14, No. 12. P. e0225913. DOI: 10.1371/journal.pone.0225913</mixed-citation></citation-alternatives></ref><ref id="B127"><label>127.</label><citation-alternatives><mixed-citation xml:lang="en">Zeng A, Yin J, Li Y, et al. miR-129-5p targets Wnt5a to block PKC/ERK/NF-κB and JNK pathways in glioblastoma. Cell Death Dis. 2018;9(3):394. DOI: 10.1038/s41419-018-0343-1</mixed-citation><mixed-citation xml:lang="ru">Zeng A., Yin J., Li Y. et al. miR-129-5p targets Wnt5a to block PKC/ERK/NF-κB and JNK pathways in glioblastoma // Cell Death Dis. 2018. Vol. 9, No. 3. P. 394. DOI: 10.1038/s41419-018-0343-1</mixed-citation></citation-alternatives></ref><ref id="B128"><label>128.</label><citation-alternatives><mixed-citation xml:lang="en">Balandeh E, Mohammadshafie K, Mahmoudi Y, et al. Roles of non-coding RNAs and angiogenesis in glioblastoma. Front Cell Dev Biol. 2021;9:716462. DOI: 10.3389/fcell.2021.716462</mixed-citation><mixed-citation xml:lang="ru">Balandeh E., Mohammadshafie K., Mahmoudi Y. et al. Roles of non-coding RNAs and angiogenesis in glioblastoma // Front. Cell Dev. Biol. 2021. Vol. 9. P. 716462. DOI: 10.3389/fcell.2021.716462</mixed-citation></citation-alternatives></ref><ref id="B129"><label>129.</label><citation-alternatives><mixed-citation xml:lang="en">Mathew LK, Huangyang P, Mucaj V, et al. Feedback circuitry between miR-218 repression and RTK activation in glioblastoma. Sci Signal. 2015;8(375):ra42. DOI: 10.1126/scisignal.2005978</mixed-citation><mixed-citation xml:lang="ru">Mathew L.K., Huangyang P., Mucaj V. et al. Feedback circuitry between miR-218 repression and RTK activation in glioblastoma // Sci. Signal. 2015. Vol. 8, No. 375. P. ra42. DOI: 10.1126/scisignal.2005978</mixed-citation></citation-alternatives></ref><ref id="B130"><label>130.</label><citation-alternatives><mixed-citation xml:lang="en">Smits M, Nilsson J, Mir SE, et al. miR-101 is down-regulated in glioblastoma resulting in EZH2-induced proliferation, migration, and angiogenesis. Oncotarget. 2010;1(8):710–720. DOI: 10.18632/oncotarget.205</mixed-citation><mixed-citation xml:lang="ru">Smits M., Nilsson J., Mir S.E. et al. miR-101 is down-regulated in glioblastoma resulting in EZH2-induced proliferation, migration, and angiogenesis // Oncotarget. 2010. Vol. 1, No. 8. P. 710–720. DOI: 10.18632/oncotarget.205</mixed-citation></citation-alternatives></ref><ref id="B131"><label>131.</label><citation-alternatives><mixed-citation xml:lang="en">Sun J, Zheng G, Gu Z, Guo Z. MiR-137 inhibits proliferation and angiogenesis of human glioblastoma cells by targeting EZH2. J Neurooncol. 2015;122:481–489. DOI: 10.1007/s11060-015-1753-x</mixed-citation><mixed-citation xml:lang="ru">Sun J., Zheng G., Gu Z., Guo Z. MiR-137 inhibits proliferation and angiogenesis of human glioblastoma cells by targeting EZH2 // J. Neurooncol. 2015. Vol. 122. P. 481–489. DOI: 10.1007/s11060-015-1753-x</mixed-citation></citation-alternatives></ref><ref id="B132"><label>132.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang J, Chen L, Han L, et al. EZH2 is a negative prognostic factor and exhibits pro-oncogenic activity in glioblastoma. Cancer Lett. 2015;356(2PtB):929–936. DOI: 10.1016/j.canlet.2014.11.003</mixed-citation><mixed-citation xml:lang="ru">Zhang J., Chen L., Han L. et al. EZH2 is a negative prognostic factor and exhibits pro-oncogenic activity in glioblastoma // Cancer Lett. 2015. Vol. 356, No. 2PtB. P. 929–936. DOI: 10.1016/j.canlet.2014.11.003</mixed-citation></citation-alternatives></ref><ref id="B133"><label>133.</label><citation-alternatives><mixed-citation xml:lang="en">Tian J-H, Mu L-J, Wang M-Y, et al. FOXM1-dependent transcriptional regulation of EZH2 induces proliferation and progression in prostate cancer. Anticancer Agents Med Chem. 2021;21(14):1835–1841. DOI: 10.2174/1871520620666200731161810</mixed-citation><mixed-citation xml:lang="ru">Tian J.-H., Mu L.-J., Wang M.-Y. et al. FOXM1-dependent transcriptional regulation of EZH2 induces proliferation and progression in prostate cancer // Anticancer Agents Med. Chem. 2021. Vol. 21, No. 14. P. 1835–1841. DOI: 10.2174/1871520620666200731161810</mixed-citation></citation-alternatives></ref><ref id="B134"><label>134.</label><citation-alternatives><mixed-citation xml:lang="en">Gouazé-Andersson V, Ghérardi M-J, Lemarié A, et al. FGFR1/FOXM1 pathway: a key regulator of glioblastoma stem cells radioresistance and a prognosis biomarker. Oncotarget. 2018;9:31637–31649. DOI: 10.18632/oncotarget.25827</mixed-citation><mixed-citation xml:lang="ru">Gouazé-Andersson V., Ghérardi M.-J., Lemarié A. et al. FGFR1/FOXM1 pathway: a key regulator of glioblastoma stem cells radioresistance and a prognosis biomarker // Oncotarget. 2018. Vol. 9. P. 31637–31649. DOI: 10.18632/oncotarget.25827</mixed-citation></citation-alternatives></ref><ref id="B135"><label>135.</label><citation-alternatives><mixed-citation xml:lang="en">Zaman N, Dass SS, Parcq P, et al. The KDR (VEGFR-2) genetic polymorphism Q472H and c-KIT polymorphism M541L are associated with more aggressive behaviour in astrocytic gliomas. Cancer Genomics Proteomics. 2020;17(6):715–727. DOI: 10.21873/cgp.20226</mixed-citation><mixed-citation xml:lang="ru">Zaman N., Dass S.S., Parcq P. et al. The KDR (VEGFR-2) genetic polymorphism Q472H and c-KIT polymorphism M541L are associated with more aggressive behaviour in astrocytic gliomas // Cancer Genomics Proteomics. 2020. Vol. 17, No. 6. P. 715–727. DOI: 10.21873/cgp.20226</mixed-citation></citation-alternatives></ref><ref id="B136"><label>136.</label><citation-alternatives><mixed-citation xml:lang="en">Yu X, Sun NR, Jang HT, et al. Associations between EGFR gene polymorphisms and susceptibility to glioma: a systematic review and meta-analysis from GWAS and case-control studies. Oncotarget. 2017;8(49):86877–86885. DOI: 10.18632/oncotarget.21011</mixed-citation><mixed-citation xml:lang="ru">Yu X., Sun N.R., Jang H.T. et al. Associations between EGFR gene polymorphisms and susceptibility to glioma: a systematic review and meta-analysis from GWAS and case-control studies // Oncotarget. 2017. Vol. 8, No. 49. P. 86877–86885. DOI: 10.18632/oncotarget.21011</mixed-citation></citation-alternatives></ref><ref id="B137"><label>137.</label><citation-alternatives><mixed-citation xml:lang="en">Zhao Y, Wang H, He C. Drug resistance of targeted therapy for advanced non-small cell lung cancer harbored EGFR mutation. From mechanism analysis to clinical strategy. J Cancer Res Clin Oncol. 2021;147(12):3653–3664. DOI: 10.1007/s00432-021-03828-8</mixed-citation><mixed-citation xml:lang="ru">Zhao Y., Wang H., He C. Drug resistance of targeted therapy for advanced non-small cell lung cancer harbored EGFR mutation. From mechanism analysis to clinical strategy // J. Cancer Res. Clin. Oncol. 2021. Vol. 147, No. 12. P. 3653–3664. DOI: 10.1007/s00432-021-03828-8</mixed-citation></citation-alternatives></ref><ref id="B138"><label>138.</label><citation-alternatives><mixed-citation xml:lang="en">Saleem H, Kulsoom Abdul U, Küçükosmanoglu A, et al. The TICking clock of EGFR therapy resistance in glioblastoma: target independence or target compensation. Drug Resist Updat. 2019;43:29–37. DOI: 10.1016/j.drup.2019.04.002</mixed-citation><mixed-citation xml:lang="ru">Saleem H., Kulsoom Abdul U., Küçükosmanoglu A. et al. The TICking clock of EGFR therapy resistance in glioblastoma: target independence or target compensation // Drug Resist. Updat. 2019. Vol. 43. P. 29–37. DOI: 10.1016/j.drup.2019.04.002</mixed-citation></citation-alternatives></ref><ref id="B139"><label>139.</label><citation-alternatives><mixed-citation xml:lang="en">Ma Y, Tang N, Thompson RC. InsR/IGF1R pathway mediates resistance to EGFR inhibitors in glioblastoma. Clin Cancer Res. 2016;22:1767–1776. DOI: 10.1158/1078-0432.CCR-15-1677</mixed-citation><mixed-citation xml:lang="ru">Ma Y., Tang N., Thompson R.C. InsR/IGF1R pathway mediates resistance to EGFR inhibitors in glioblastoma // Clin. Cancer Res. 2016. Vol. 22. P. 1767–1776. DOI: 10.1158/1078-0432.CCR-15-1677</mixed-citation></citation-alternatives></ref><ref id="B140"><label>140.</label><citation-alternatives><mixed-citation xml:lang="en">Akhavan D, Pourzia AL, Nourian AA, et al. De-repression of PDGFRβ transcription promotes acquired resistance to EGFR tyrosine kinase inhibitors in glioblastoma patients. Cancer Discov. 2013;3(5):534–547. DOI: 10.1158/2159-8290.CD-12-0502</mixed-citation><mixed-citation xml:lang="ru">Akhavan D., Pourzia A.L., Nourian A.A. et al. De-repression of PDGFRβ transcription promotes acquired resistance to EGFR tyrosine kinase inhibitors in glioblastoma patients // Cancer Discov. 2013. Vol. 3, No. 5. P. 534–547. DOI: 10.1158/2159-8290.CD-12-0502</mixed-citation></citation-alternatives></ref><ref id="B141"><label>141.</label><citation-alternatives><mixed-citation xml:lang="en">Song K, Yuan Y, Lin Y, et al. ERBB3, IGF1R, and TGFBR2 expression correlate with PDGFR expression in glioblastoma and participate in PDGFR inhibitor resistance of glioblastoma cells. Am J Cancer Res. 2018;8(5):792–809.</mixed-citation><mixed-citation xml:lang="ru">Song K., Yuan Y., Lin Y. et al. ERBB3, IGF1R, and TGFBR2 expression correlate with PDGFR expression in glioblastoma and participate in PDGFR inhibitor resistance of glioblastoma cells // Am. J. Cancer Res. 2018. Vol. 8, No. 5. P. 792–809.</mixed-citation></citation-alternatives></ref><ref id="B142"><label>142.</label><citation-alternatives><mixed-citation xml:lang="en">Almiron Bonnin DA, Ran C, Havrda MC. Insulin-mediated signaling facilitates resistance to PDGFR inhibition in proneural hPDGFB-driven gliomas. Mol Cancer Ther. 2017;16:705–716. DOI: 10.1158/1535-7163.MCT-16-0616</mixed-citation><mixed-citation xml:lang="ru">Almiron Bonnin D.A., Ran C., Havrda M.C. Insulin-mediated signaling facilitates resistance to PDGFR inhibition in proneural hPDGFB-driven gliomas // Mol. Cancer Ther. 2017. Vol. 16. P. 705–716. DOI: 10.1158/1535-7163.MCT-16-0616</mixed-citation></citation-alternatives></ref><ref id="B143"><label>143.</label><citation-alternatives><mixed-citation xml:lang="en">Pullen NA, Pickford AR, Perry MM, et al. Current insights into matrix metalloproteinases and glioma progression: transcending the degradation boundary. Metalloproteinases In Medicine. 2018;2018(5):13–30. DOI: 10.2147/MNM.S105123</mixed-citation><mixed-citation xml:lang="ru">Pullen N.A., Pickford A.R., Perry M.M. et al. Current insights into matrix metalloproteinases and glioma progression: transcending the degradation boundary // Metalloproteinases in Medicine. 2018. Vol. 2018, No. 5. P. 13–30. DOI: 10.2147/MNM.S105123</mixed-citation></citation-alternatives></ref><ref id="B144"><label>144.</label><citation-alternatives><mixed-citation xml:lang="en">Xu S, Xu H, Wang W, et al. The role of collagen in cancer: from bench to bedside. J Transl Med. 2019;17:309. DOI: 10.1186/s12967-019-2058-1</mixed-citation><mixed-citation xml:lang="ru">Xu S., Xu H., Wang W. et al. The role of collagen in cancer: from bench to bedside // J. Transl. Med. 2019. Vol. 17. P. 309. DOI: 10.1186/s12967-019-2058-1</mixed-citation></citation-alternatives></ref><ref id="B145"><label>145.</label><citation-alternatives><mixed-citation xml:lang="en">Mooney KL, Choy W, Sidhu S, et al. The role of CD44 in glioblastoma multiforme. J Clin Neurosci. 2016;34:1–5. DOI: 10.1016/j.jocn.2016.05.012</mixed-citation><mixed-citation xml:lang="ru">Mooney K.L., Choy W., Sidhu S. et al. The role of CD44 in glioblastoma multiforme // J. Clin. Neurosci. 2016. Vol. 34. P. 1–5. DOI: 10.1016/j.jocn.2016.05.012</mixed-citation></citation-alternatives></ref><ref id="B146"><label>146.</label><citation-alternatives><mixed-citation xml:lang="en">Urbantat RM, Blank A, Kremenetskaia I. The CXCL2/IL8/CXCR2 pathway is relevant for brain tumor malignancy and endothelial cell function. Int J Mol Sci. 2021;22(5):2634. DOI: 10.3390/ijms22052634</mixed-citation><mixed-citation xml:lang="ru">Urbantat R.M., Blank A., Kremenetskaia I. The CXCL2/IL8/CXCR2 pathway is relevant for brain tumor malignancy and endothelial cell function // Int. J. Mol. Sci. 2021. Vol. 22, No. 5. P. 2634. DOI: 10.3390/ijms22052634</mixed-citation></citation-alternatives></ref><ref id="B147"><label>147.</label><citation-alternatives><mixed-citation xml:lang="en">Bordji K, Grandval A, Cuhna-Alves L, et al. Hypoxia-inducible factor-2α (HIF-2α), but not HIF-1α, is essential for hypoxic induction of class III β-tubulin expression in human glioblastoma cells. FEBS J. 2014;281(23):5220–5236. DOI: 10.1111/febs.13062</mixed-citation><mixed-citation xml:lang="ru">Bordji K., Grandval A., Cuhna-Alves L. et al. Hypoxia-inducible factor-2α (HIF-2α), but not HIF-1α, is essential for hypoxic induction of class III β-tubulin expression in human glioblastoma cells // FEBS J. 2014. Vol. 281, No. 23. P. 5220–5236. DOI: 10.1111/febs.13062</mixed-citation></citation-alternatives></ref><ref id="B148"><label>148.</label><citation-alternatives><mixed-citation xml:lang="en">Chou CW, Wang CC, Wu CP, et al. Tumor cycling hypoxia induces chemoresistance in glioblastoma multiforme by upregulating the expression and function of ABCB1. Neurooncol. 2012;14(10):1227–1238. DOI: 10.1093/neuonc/nos195</mixed-citation><mixed-citation xml:lang="ru">Chou C.W., Wang C.C., Wu C.P. et al. Tumor cycling hypoxia induces chemoresistance in glioblastoma multiforme by upregulating the expression and function of ABCB1 // Neurooncol. 2012. Vol. 14, No. 10. P. 1227–1238. DOI: 10.1093/neuonc/nos195</mixed-citation></citation-alternatives></ref><ref id="B149"><label>149.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang L, Yang H, Zhang W, et al. Clk1 -regulated aerobic glycolysis is involved in gliomas chemoresistance. J Neurochem. 2017;142(4):574–588. DOI: 10.1111/jnc.14096</mixed-citation><mixed-citation xml:lang="ru">Zhang L., Yang H., Zhang W. et al. Clk1 -regulated aerobic glycolysis is involved in gliomas chemoresistance // J. Neurochem. 2017. Vol. 142, No. 4. P. 574–588. DOI: 10.1111/jnc.14096</mixed-citation></citation-alternatives></ref><ref id="B150"><label>150.</label><citation-alternatives><mixed-citation xml:lang="en">Kang W, Kim SH, Cho HJ, et al. Talin1 targeting potentiates anti-angiogenic therapy by attenuating invasion and stem-like features of glioblastoma multiforme. Oncotarget. 2015;6(29):27239–27251. DOI: 10.18632/oncotarget.4835</mixed-citation><mixed-citation xml:lang="ru">Kang W., Kim S.H., Cho H.J. et al. Talin1 targeting potentiates anti-angiogenic therapy by attenuating invasion and stem-like features of glioblastoma multiforme // Oncotarget. 2015. Vol. 6, No. 29. P. 27239–27251. DOI: 10.18632/oncotarget.4835</mixed-citation></citation-alternatives></ref><ref id="B151"><label>151.</label><citation-alternatives><mixed-citation xml:lang="en">Matini AH, Naeini MM, Kashani HH, et al. Evaluation of Nestin and EGFR in patients with glioblastoma multiforme in a public hospital in Iran. Asian Pac J Cancer Prev. 2020;21(10):2889–2894. DOI: 10.31557/APJCP.2020.21.10.2889</mixed-citation><mixed-citation xml:lang="ru">Matini A.H., Naeini M.M., Kashani H.H. et al. Evaluation of Nestin and EGFR in patients with glioblastoma multiforme in a public hospital in Iran // Asian Pac. J. Cancer Prev. 2020. Vol. 21, No. 10. P. 2889–2894. DOI: 10.31557/APJCP.2020.21.10.2889</mixed-citation></citation-alternatives></ref><ref id="B152"><label>152.</label><citation-alternatives><mixed-citation xml:lang="en">Ahmed EM, Bandopadhyay G, Coyle B, Grabowska A. A HIF-independent, CD133-mediated mechanism of cisplatin resistance in glioblastoma cells. Cell Oncol (Dordr). 2018;41(3):319–328. DOI: 10.1007/s13402-018-0374-8</mixed-citation><mixed-citation xml:lang="ru">Ahmed E.M., Bandopadhyay G., Coyle B., Grabowska A. A HIF-independent, CD133-mediated mechanism of cisplatin resistance in glioblastoma cells // Cell Oncol. (Dordr). 2018. Vol. 41, No. 3. P. 319–328. DOI: 10.1007/s13402-018-0374-8</mixed-citation></citation-alternatives></ref><ref id="B153"><label>153.</label><citation-alternatives><mixed-citation xml:lang="en">Suvasini R, Shruti B, Thota B, et al. Insulin growth factor-2 binding protein 3 (IGF2BP3) is a glioblastoma-specific marker that activates phosphatidylinositol 3-kinase/mitogen-activated protein kinase (PI3K/MAPK) pathways by modulating IGF-2. J Biol Chem. 2011;286(29):25882–25890. DOI: 10.1074/jbc.M110.178012</mixed-citation><mixed-citation xml:lang="ru">Suvasini R., Shruti B., Thota B. et al. Insulin growth factor-2 binding protein 3 (IGF2BP3) is a glioblastoma-specific marker that activates phosphatidylinositol 3-kinase/mitogen-activated protein kinase (PI3K/MAPK) pathways by modulating IGF-2 // J. Biol. Chem. 2011. Vol. 286, No. 29. P. 25882–25890. DOI: 10.1074/jbc.M110.178012</mixed-citation></citation-alternatives></ref><ref id="B154"><label>154.</label><citation-alternatives><mixed-citation xml:lang="en">Womeldorff M, Gillespie D, Jensen RL. Hypoxia-inducible factor-1 and associated upstream and downstream proteins in the pathophysiology and management of glioblastoma. Neurosurg Focus. 2014;37(6):E8. DOI: 10.3171/2014.9.focus14496</mixed-citation><mixed-citation xml:lang="ru">Womeldorff M., Gillespie D., Jensen R.L. Hypoxia-inducible factor-1 and associated upstream and downstream proteins in the pathophysiology and management of glioblastoma // Neurosurg. Focus. 2014. Vol. 37, No. 6. P. E8. DOI: 10.3171/2014.9.focus14496</mixed-citation></citation-alternatives></ref><ref id="B155"><label>155.</label><citation-alternatives><mixed-citation xml:lang="en">Chen X-C, Wei X-T, Guan J-H, et al. EGF stimulates glioblastoma metastasis by induction of matrix metalloproteinase-9 in an EGFR-dependent mechanism. Oncotarget. 2017;8(39):65969–65982. DOI: 10.18632/oncotarget.19622</mixed-citation><mixed-citation xml:lang="ru">Chen X.-C., Wei X.-T., Guan J.-H. et al. EGF stimulates glioblastoma metastasis by induction of matrix metalloproteinase-9 in an EGFR-dependent mechanism // Oncotarget. 2017. Vol. 8, No. 39. P. 65969–65982. DOI: 10.18632/oncotarget.19622</mixed-citation></citation-alternatives></ref><ref id="B156"><label>156.</label><citation-alternatives><mixed-citation xml:lang="en">Rogers AE, Le JP, Sather S, et al. Mer receptor tyrosine kinase inhibition impedes glioblastoma multiforme migration and alters cellular morphology. Oncogene. 2012;31(38):4171–4181. DOI: 10.1038/onc.2011.588</mixed-citation><mixed-citation xml:lang="ru">Rogers A.E., Le J.P., Sather S. et al. Mer receptor tyrosine kinase inhibition impedes glioblastoma multiforme migration and alters cellular morphology // Oncogene. 2012. Vol. 31, No. 38. P. 4171–4181. DOI: 10.1038/onc.2011.588</mixed-citation></citation-alternatives></ref><ref id="B157"><label>157.</label><citation-alternatives><mixed-citation xml:lang="en">Wang Y, Moncayo G, Morin P, et al. Mer receptor tyrosine kinase promotes invasion and survival in glioblastoma multiforme. Oncogene. 2013;32:872–882. DOI: 10.1038/onc.2012.104</mixed-citation><mixed-citation xml:lang="ru">Wang Y., Moncayo G., Morin P. et al. Mer receptor tyrosine kinase promotes invasion and survival in glioblastoma multiforme // Oncogene. 2013. Vol. 32. P. 872–882. DOI: 10.1038/onc.2012.104</mixed-citation></citation-alternatives></ref><ref id="B158"><label>158.</label><citation-alternatives><mixed-citation xml:lang="en">Wislet S, Vandervelden G, Rogister B. From neural crest development to cancer and vice versa: How p75 NTR and (Pro)neurotrophins could act on cell migration and invasion? Front Mol Neurosci. 2018;11:244. DOI: 10.3389/fnmol.2018.00244</mixed-citation><mixed-citation xml:lang="ru">Wislet S., Vandervelden G., Rogister B. From neural crest development to cancer and vice versa: How p75 NTR and (Pro)neurotrophins could act on cell migration and invasion? // Front. Mol. Neurosci. 2018. Vol. 11. P. 244. DOI: 10.3389/fnmol.2018.00244</mixed-citation></citation-alternatives></ref><ref id="B159"><label>159.</label><citation-alternatives><mixed-citation xml:lang="en">Yang W, Wu PF, Ma JX, et al. Sortilin promotes glioblastoma invasion and mesenchymal transition through GSK-3β/β-catenin/twist pathway. Cell Death Dis. 2019;10:208. DOI: 10.1038/s41419-019-1449-9</mixed-citation><mixed-citation xml:lang="ru">Yang W., Wu P.F., Ma J.X. et al. Sortilin promotes glioblastoma invasion and mesenchymal transition through GSK-3β/β-catenin/twist pathway // Cell Death Dis. 2019. Vol. 10. P. 208. DOI: 10.1038/s41419-019-1449-9</mixed-citation></citation-alternatives></ref><ref id="B160"><label>160.</label><citation-alternatives><mixed-citation xml:lang="en">Brown MC, Staniszewska I, Lazarovici P, et al. Regulatory effect of nerve growth factor in α9β1 integrin–dependent progression of glioblastoma. Neuro Oncol. 2008;10(6):968–980. DOI: 10.1215/15228517-2008-047</mixed-citation><mixed-citation xml:lang="ru">Brown M.C., Staniszewska I., Lazarovici P. et al. Regulatory effect of nerve growth factor in α9β1 integrin–dependent progression of glioblastoma // Neuro. Oncol. 2008. Vol. 10, No. 6. P. 968–980. DOI: 10.1215/15228517-2008-047</mixed-citation></citation-alternatives></ref><ref id="B161"><label>161.</label><citation-alternatives><mixed-citation xml:lang="en">Qi Q, He K, Liu X, et al. Disrupting the PIKE-A/Akt interaction inhibits glioblastoma cell survival, migration, invasion and colony formation. Oncogene. 2013;32(8):1030–1040. DOI: 10.1038/onc.2012.109</mixed-citation><mixed-citation xml:lang="ru">Qi Q., He K., Liu X. et al. Disrupting the PIKE-A/Akt interaction inhibits glioblastoma cell survival, migration, invasion and colony formation // Oncogene. 2013. Vol. 32, No. 8. P. 1030–1040. DOI: 10.1038/onc.2012.109</mixed-citation></citation-alternatives></ref><ref id="B162"><label>162.</label><citation-alternatives><mixed-citation xml:lang="en">So J-S, Kim H, Han K-S. Mechanisms of invasion in glioblastoma: extracellular matrix, Ca2+ signaling, and glutamate. Front Cell Neurosci. 2021;15:663092. DOI: 10.3389/fncel.2021.663092</mixed-citation><mixed-citation xml:lang="ru">So J.-S., Kim H., Han K.-S. Mechanisms of invasion in glioblastoma: extracellular matrix, Ca2+ signaling, and glutamate // Front. Cell Neurosci. 2021. Vol. 15. P. 663092. DOI: 10.3389/fncel.2021.663092</mixed-citation></citation-alternatives></ref><ref id="B163"><label>163.</label><citation-alternatives><mixed-citation xml:lang="en">Raychaudhuri B, Han Y, Lu T, et al. Aberrant constitutive activation of nuclear factor κB in glioblastoma multiforme drives invasive phenotype. J Neurooncol. 2007;85(1):39–47. DOI: 10.1007/s11060-007-9390-7</mixed-citation><mixed-citation xml:lang="ru">Raychaudhuri B., Han Y., Lu T. et al. Aberrant constitutive activation of nuclear factor κB in glioblastoma multiforme drives invasive phenotype // J. Neurooncol. 2007. Vol. 85, No. 1. P. 39–47. DOI: 10.1007/s11060-007-9390-7</mixed-citation></citation-alternatives></ref><ref id="B164"><label>164.</label><citation-alternatives><mixed-citation xml:lang="en">Shan Q, Li S, Cao Q, et al. Inhibition of chromosomal region maintenance 1 suppresses the migration and invasion of glioma cells via inactivation of the STAT3/MMP2 signaling pathway. Korean J Physiol Pharmacol. 2020;24(3):193–201. DOI: 10.4196/kjpp.2020.24.3.193</mixed-citation><mixed-citation xml:lang="ru">Shan Q., Li S., Cao Q. et al. Inhibition of chromosomal region maintenance 1 suppresses the migration and invasion of glioma cells via inactivation of the STAT3/MMP2 signaling pathway // Korean J. Physiol. Pharmacol. 2020. Vol. 24, No. 3. P. 193–201. DOI: 10.4196/kjpp.2020.24.3.193</mixed-citation></citation-alternatives></ref><ref id="B165"><label>165.</label><citation-alternatives><mixed-citation xml:lang="en">Brantley EC, Benveniste EN. Signal transducer and activator of transcription-3: a molecular hub for signaling pathways in gliomas. Mol Cancer Res. 2008;6(5):675–684. DOI: 10.1158/1541-7786.MCR-07-2180</mixed-citation><mixed-citation xml:lang="ru">Brantley E.C., Benveniste E.N. Signal transducer and activator of transcription-3: a molecular hub for signaling pathways in gliomas // Mol. Cancer Res. 2008. Vol. 6, No. 5. P. 675–684. DOI: 10.1158/1541-7786.MCR-07-2180</mixed-citation></citation-alternatives></ref><ref id="B166"><label>166.</label><citation-alternatives><mixed-citation xml:lang="en">Cheng M, Zeng Y, Zhang T, et al. Transcription factor ELF1 activates MEIS1 transcription and then regulates the GFI1/FBW7 axis to promote the development of glioma. Mol Ther Nucleic Acids. 2020;23:418–430. DOI: 10.1016/j.omtn.2020.10.015</mixed-citation><mixed-citation xml:lang="ru">Cheng M., Zeng Y., Zhang T. et al. Transcription factor ELF1 activates MEIS1 transcription and then regulates the GFI1/FBW7 axis to promote the development of glioma // Mol. Ther. Nucleic. Acids. 2020. Vol. 23. P. 418–430. DOI: 10.1016/j.omtn.2020.10.015</mixed-citation></citation-alternatives></ref><ref id="B167"><label>167.</label><citation-alternatives><mixed-citation xml:lang="en">Ma J, Wang P, Liu Y, et al. Krüppel-like factor 4 regulates blood-tumor barrier permeability via ZO-1, occludin and claudin-5. J Cell Physiol. 2014;229(7):916–926. DOI: 10.1002/jcp.24523</mixed-citation><mixed-citation xml:lang="ru">Ma J., Wang P., Liu Y. et al. Krüppel-like factor 4 regulates blood-tumor barrier permeability via ZO-1, occludin and claudin-5 // J. Cell. Physiol. 2014;229(7):916–926. DOI: 10.1002/jcp.24523</mixed-citation></citation-alternatives></ref><ref id="B168"><label>168.</label><citation-alternatives><mixed-citation xml:lang="en">Chen H, Lu Q, Fei X, et al. miR-22 inhibits the proliferation, motility, and invasion of human glioblastoma cells by directly targeting SIRT1. Tumour Biol. 2016;37(5):6761–6768. DOI: 10.1007/s13277-015-4575-8</mixed-citation><mixed-citation xml:lang="ru">Chen H., Lu Q., Fei X. et al. miR-22 inhibits the proliferation, motility, and invasion of human glioblastoma cells by directly targeting SIRT1 // Tumour Biol. 2016. Vol. 37, No. 5. P. 6761–6768. DOI: 10.1007/s13277-015-4575-8</mixed-citation></citation-alternatives></ref><ref id="B169"><label>169.</label><citation-alternatives><mixed-citation xml:lang="en">Chakrabarti M, Ray SK. Direct transfection of miR-137 mimics is more effective than DNA demethylation of miR-137 promoter to augment anti-tumor mechanisms of delphinidin in human glioblastoma U87MG and LN18 cells. Gene. 2015;573(1):141–152. DOI: 10.1016/j.gene.2015.07.034</mixed-citation><mixed-citation xml:lang="ru">Chakrabarti M., Ray S.K. Direct transfection of miR-137 mimics is more effective than DNA demethylation of miR-137 promoter to augment anti-tumor mechanisms of delphinidin in human glioblastoma U87MG and LN18 cells // Gene. 2015. Vol. 573, No. 1. P. 141–152. DOI: 10.1016/j.gene.2015.07.034</mixed-citation></citation-alternatives></ref><ref id="B170"><label>170.</label><citation-alternatives><mixed-citation xml:lang="en">Lv S, Sun B, Dai C, et al. The downregulation of MicroRNA-146a modulates TGF-beta signaling pathways activity in glioblastoma. Mol Neurobiol. 2015;52(3):1257–1262. DOI: 10.1007/s12035-014-8938-8</mixed-citation><mixed-citation xml:lang="ru">Lv S., Sun B., Dai C. et al. The downregulation of MicroRNA-146a modulates TGF-beta signaling pathways activity in glioblastoma // Mol. Neurobiol. 2015. Vol. 52, No. 3. P. 1257–1262. DOI: 10.1007/s12035-014-8938-8</mixed-citation></citation-alternatives></ref><ref id="B171"><label>171.</label><citation-alternatives><mixed-citation xml:lang="en">Katakowski M, Zheng X, Jiang F, et al. MiR-146b-5p suppresses EGFR expression and reduces in vitro migration and invasion of glioma. Cancer Invest. 2010;28(10):1024–1030. DOI: 10.3109/07357907.2010.512596</mixed-citation><mixed-citation xml:lang="ru">Katakowski M., Zheng X., Jiang F. et al. MiR-146b-5p suppresses EGFR expression and reduces in vitro migration and invasion of glioma // Cancer Invest. 2010. Vol. 28, No. 10. P. 1024–1030. DOI: 10.3109/07357907.2010.512596</mixed-citation></citation-alternatives></ref><ref id="B172"><label>172.</label><citation-alternatives><mixed-citation xml:lang="en">Rao SA, Arimappamagan A, Pandey P, et al. miR-219-5p inhibits receptor tyrosine kinase pathway by targeting EGFR in glioblastoma. PLoS One. 2013;8(5):e63164. DOI: 10.1371/journal.pone.0063164</mixed-citation><mixed-citation xml:lang="ru">Rao S.A., Arimappamagan A., Pandey P. et al. miR-219-5p inhibits receptor tyrosine kinase pathway by targeting EGFR in glioblastoma // PLoS One. 2013. Vol. 8, No. 5. P. e63164. DOI: 10.1371/journal.pone.0063164</mixed-citation></citation-alternatives></ref><ref id="B173"><label>173.</label><citation-alternatives><mixed-citation xml:lang="en">Gao Y, Yu H, Liu Y, et al. Long non-coding RNA HOXA-AS2 regulates malignant glioma behaviors and vasculogenic mimicry formation via the MiR-373/EGFR Axis. Cell Physiol Biochem. 2018;45(1):131–147. DOI: 10.1159/000486253</mixed-citation><mixed-citation xml:lang="ru">Gao Y., Yu H., Liu Y. et al. Long non-coding RNA HOXA-AS2 regulates malignant glioma behaviors and vasculogenic mimicry formation via the MiR-373/EGFR Axis. Cell. Physiol. Biochem. 2018;45(1):131–147. DOI: 10.1159/000486253</mixed-citation></citation-alternatives></ref><ref id="B174"><label>174.</label><citation-alternatives><mixed-citation xml:lang="en">Zhou XY, Liu H, Ding ZB, et al. lncRNA SNHG16 promotes glioma tumorigenicity through miR-373/EGFR axis by activating PI3K/AKT pathway. Genomics. 2020;112(1):1021–1029. DOI: 10.1016/j.ygeno.2019.06.017</mixed-citation><mixed-citation xml:lang="ru">Zhou X.Y., Liu H., Ding Z.B. et al. lncRNA SNHG16 promotes glioma tumorigenicity through miR-373/EGFR axis by activating PI3K/AKT pathway // Genomics. 2020. Vol. 112, No. 1. P. 1021–1029. DOI: 10.1016/j.ygeno.2019.06.017</mixed-citation></citation-alternatives></ref><ref id="B175"><label>175.</label><citation-alternatives><mixed-citation xml:lang="en">Pan DS, Cao P, Li JJ, et al. MicroRNA-374b inhibits migration and invasion of glioma cells by targeting EGFR. Eur Rev Med Pharmacol Sci. 2019;23(10):4254–4263. DOI: 10.26355/eurrev_201905_17930</mixed-citation><mixed-citation xml:lang="ru">Pan D.S., Cao P., Li J.J. et al. MicroRNA-374b inhibits migration and invasion of glioma cells by targeting EGFR // Eur. Rev. Med. Pharmacol. Sci. 2019. Vol. 23, No. 10. P. 4254–4263. DOI: 10.26355/eurrev_201905_17930</mixed-citation></citation-alternatives></ref><ref id="B176"><label>176.</label><citation-alternatives><mixed-citation xml:lang="en">Li X, Liu Y, Granberg KJ, et al. Two mature products of MIR-491 coordinate to suppress key cancer hallmarks in glioblastoma. Oncogene. 2015;34(13):1619–1628. DOI: 10.1038/onc.2014.98</mixed-citation><mixed-citation xml:lang="ru">Li X., Liu Y., Granberg K.J. et al. Two mature products of MIR-491 coordinate to suppress key cancer hallmarks in glioblastoma // Oncogene. 2015. Vol. 34, No. 13. P. 1619–1628. DOI: 10.1038/onc.2014.98</mixed-citation></citation-alternatives></ref><ref id="B177"><label>177.</label><citation-alternatives><mixed-citation xml:lang="en">Jiang C, Shen F, Du J, et al. MicroRNA-564 is downregulated in glioblastoma and inhibited proliferation and invasion of glioblastoma cells by targeting TGF-beta1. Oncotarget. 2016;7(35):56200–56208. DOI: 10.18632/oncotarget.8987</mixed-citation><mixed-citation xml:lang="ru">Jiang C., Shen F., Du J. et al. MicroRNA-564 is downregulated in glioblastoma and inhibited proliferation and invasion of glioblastoma cells by targeting TGF-beta1 // Oncotarget. 2016. Vol. 7, No. 35. P. 56200–56208. DOI: 10.18632/oncotarget.8987</mixed-citation></citation-alternatives></ref><ref id="B178"><label>178.</label><citation-alternatives><mixed-citation xml:lang="en">Ji Y, Sun Q, Zhang J, Hu H. MiR-615 inhibits cell proliferation, migration and invasion by targeting EGFR in human glioblastoma. Biochem Biophys Res Commun. 2018;499(3):719–726. DOI: 10.1016/j.bbrc.2018.03.217</mixed-citation><mixed-citation xml:lang="ru">Ji Y., Sun Q., Zhang J., Hu H. MiR-615 inhibits cell proliferation, migration and invasion by targeting EGFR in human glioblastoma // Biochem. Biophys. Res. Commun. 2018. Vol. 499, No. 3. P. 719–726. DOI: 10.1016/j.bbrc.2018.03.217</mixed-citation></citation-alternatives></ref><ref id="B179"><label>179.</label><citation-alternatives><mixed-citation xml:lang="en">Wang F, Xiao W, Sun J, et al. MiRNA-181c inhibits EGFR-signaling-dependent MMP9 activation via suppressing Akt phosphorylation in glioblastoma. Tumour Biol. 2014;35(9):8653–8658. DOI: 10.1007/s13277-014-2131-6</mixed-citation><mixed-citation xml:lang="ru">Wang F., Xiao W., Sun J. et al. MiRNA-181c inhibits EGFR-signaling-dependent MMP9 activation via suppressing Akt phosphorylation in glioblastoma // Tumour Biol. 2014. Vol. 35, No. 9. P. 8653–8658. DOI: 10.1007/s13277-014-2131-6</mixed-citation></citation-alternatives></ref><ref id="B180"><label>180.</label><citation-alternatives><mixed-citation xml:lang="en">Lu Y, Chopp M, Zheng X, et al. Overexpression of miR145 in U87 cells reduces glioma cell malignant phenotype and promotes survival after in vivo implantation. Int J Oncol. 2015;46(3):1031–1038. DOI: 10.3892/ijo.2014.2807</mixed-citation><mixed-citation xml:lang="ru">Lu Y., Chopp M., Zheng X. et al. Overexpression of miR145 in U87 cells reduces glioma cell malignant phenotype and promotes survival after in vivo implantation // Int. J. Oncol. 2015. Vol. 46, No. 3. P. 1031–1038. DOI: 10.3892/ijo.2014.2807</mixed-citation></citation-alternatives></ref><ref id="B181"><label>181.</label><citation-alternatives><mixed-citation xml:lang="en">Lu Y, Chopp M, Zheng X, et al. MiR-145 reduces ADAM17 expression and inhibits in vitro migration and invasion of glioma cells. Oncol Rep. 2013;29(1):67–72. DOI: 10.3892/or.2012.2084</mixed-citation><mixed-citation xml:lang="ru">Lu Y., Chopp M., Zheng X. et al. MiR-145 reduces ADAM17 expression and inhibits in vitro migration and invasion of glioma cells // Oncol. Rep. 2013. Vol. 29, No. 1. P. 67–72. DOI: 10.3892/or.2012.2084</mixed-citation></citation-alternatives></ref><ref id="B182"><label>182.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang KL, Zhou X, Han L, et al. MicroRNA-566 activates EGFR signaling and its inhibition sensitizes glioblastoma cells to nimotuzumab. Mol Cancer. 2014;13:63. DOI: 10.1186/1476-4598-13-63</mixed-citation><mixed-citation xml:lang="ru">Zhang K.L., Zhou X., Han L. et al. MicroRNA-566 activates EGFR signaling and its inhibition sensitizes glioblastoma cells to nimotuzumab // Mol. Cancer. 2014. Vol. 13. P. 63. DOI: 10.1186/1476-4598-13-63</mixed-citation></citation-alternatives></ref><ref id="B183"><label>183.</label><citation-alternatives><mixed-citation xml:lang="en">Zhao K, Wang Q, Wang Y, et al. EGFR/c-myc axis regulates TGFbeta/Hippo/Notch pathway via epigenetic silencing miR-524 in gliomas. Cancer Lett. 2017;406:12–21. DOI: 10.1016/j.canlet.2017.07.022</mixed-citation><mixed-citation xml:lang="ru">Zhao K., Wang Q., Wang Y. et al. EGFR/c-myc axis regulates TGFbeta/Hippo/Notch pathway via epigenetic silencing miR-524 in gliomas // Cancer Lett. 2017. Vol. 406. P. 12–21. DOI: 10.1016/j.canlet.2017.07.022</mixed-citation></citation-alternatives></ref><ref id="B184"><label>184.</label><citation-alternatives><mixed-citation xml:lang="en">Yin D, Ogawa S, Kawamata N, et al. miR-34a functions as a tumor suppressor modulating EGFR in glioblastoma multiforme. Oncogene. 2013;32(9):1155–1163. DOI: 10.1038/onc.2012.132</mixed-citation><mixed-citation xml:lang="ru">Yin D., Ogawa S., Kawamata N. et al. miR-34a functions as a tumor suppressor modulating EGFR in glioblastoma multiforme // Oncogene. 2013. Vol. 32, No. 9. P. 1155–1163. DOI: 10.1038/onc.2012.132</mixed-citation></citation-alternatives></ref><ref id="B185"><label>185.</label><citation-alternatives><mixed-citation xml:lang="en">Kim J, Zhang Y, Skalski M, et al. microRNA-148a is a prognostic oncomiR that targets MIG6 and BIM to regulate EGFR and apoptosis in glioblastoma. Cancer Res. 2014;74(5):1541–1553. DOI: 10.1158/0008-5472.CAN-13-1449</mixed-citation><mixed-citation xml:lang="ru">Kim J., Zhang Y., Skalski M. et al. microRNA-148a is a prognostic oncomiR that targets MIG6 and BIM to regulate EGFR and apoptosis in glioblastoma // Cancer Res. 2014. Vol. 74. No. 5. P. 1541–1553. DOI: 10.1158/0008-5472.CAN-13-1449</mixed-citation></citation-alternatives></ref><ref id="B186"><label>186.</label><citation-alternatives><mixed-citation xml:lang="en">Chai C, Song LJ, Han SY, et al. MicroRNA-21 promotes glioma cell proliferation and inhibits senescence and apoptosis by targeting SPRY1 via the PTEN/PI3K/AKT signaling pathway. CNS Neurosci Ther. 2018;24(5):369–380. DOI: 10.1111/cns.12785</mixed-citation><mixed-citation xml:lang="ru">Chai C., Song L.J., Han S.Y. et al. MicroRNA-21 promotes glioma cell proliferation and inhibits senescence and apoptosis by targeting SPRY1 via the PTEN/PI3K/AKT signaling pathway // CNS Neurosci. Ther. 2018. Vol. 24, No. 5. P. 369–380. DOI: 10.1111/cns.12785</mixed-citation></citation-alternatives></ref><ref id="B187"><label>187.</label><citation-alternatives><mixed-citation xml:lang="en">Kwak SY, Kim BY, Ahn HJ, et al. Ionizing radiation-inducible miR-30e promotes glioma cell invasion through EGFR stabilization by directly targeting CBL-B. FEBS J. 2015;282(8):1512–1525. DOI: 10.1016/j.gene.2015.07.034</mixed-citation><mixed-citation xml:lang="ru">Kwak S.Y., Kim B.Y., Ahn H.J. et al. Ionizing radiation-inducible miR-30e promotes glioma cell invasion through EGFR stabilization by directly targeting CBL-B // FEBS J. 2015. Vol. 282, No. 8. P. 1512–1525. DOI: 10.1016/j.gene.2015.07.034</mixed-citation></citation-alternatives></ref><ref id="B188"><label>188.</label><citation-alternatives><mixed-citation xml:lang="en">Kwak SY, Yang JS, Kim BY, et al. Ionizing radiation-inducible miR-494 promotes glioma cell invasion through EGFR stabilization by targeting p190B rhoGAP. Biochim Biophys Acta. 2014;1843(3):508–516. DOI: 10.1016/j.bbamcr.2013.11.021</mixed-citation><mixed-citation xml:lang="ru">Kwak S.Y., Yang J.S., Kim B.Y. et al. Ionizing radiation-inducible miR-494 promotes glioma cell invasion through EGFR stabilization by targeting p190B rhoGAP // Biochim. Biophys. Acta. 2014. Vol. 1843, No. 3. P. 508–516. DOI: 10.1016/j.bbamcr.2013.11.021</mixed-citation></citation-alternatives></ref><ref id="B189"><label>189.</label><citation-alternatives><mixed-citation xml:lang="en">Munoz JL, Rodriguez-Cruz V, Greco SJ, et al. Temozolomide resistance in glioblastoma cells occurs partly through epidermal growth factor receptor mediated induction of connexin 43. Cell Death Dis. 2014;5(3):e1145. DOI: 10.1038/cddis.2014.111</mixed-citation><mixed-citation xml:lang="ru">Munoz J.L., Rodriguez-Cruz V., Greco S.J. et al. Temozolomide resistance in glioblastoma cells occurs partly through epidermal growth factor receptor mediated induction of connexin 43 // Cell Death Dis. 2014. Vol. 5, No. 3. P. e1145. DOI: 10.1038/cddis.2014.111</mixed-citation></citation-alternatives></ref><ref id="B190"><label>190.</label><citation-alternatives><mixed-citation xml:lang="en">Wang H, Wang Y, Jiang C. Stromal protein periostin identified as a progression associated and prognostic biomarker in glioma via inducing an invasive and proliferative phenotype. Int J Oncol. 2013;42(5):1716–1724. DOI: 10.3892/ijo.2013.1847</mixed-citation><mixed-citation xml:lang="ru">Wang H., Wang Y., Jiang C. Stromal protein periostin identified as a progression associated and prognostic biomarker in glioma via inducing an invasive and proliferative phenotype // Int. J. Oncol. 2013. Vol. 42, No. 5. P. 1716–1724. DOI: 10.3892/ijo.2013.1847</mixed-citation></citation-alternatives></ref><ref id="B191"><label>191.</label><citation-alternatives><mixed-citation xml:lang="en">Ketchen SE, Gamboa-Esteves FO, Lawler SE, et al. Drug resistance in glioma cells induced by a mesenchymal-amoeboid migratory switch. Biomedicines. 2021;10(1):9. DOI: 10.3390/biomedicines10010009</mixed-citation><mixed-citation xml:lang="ru">Ketchen S.E., Gamboa-Esteves F.O., Lawler S.E. et al. Drug resistance in glioma cells induced by a mesenchymal-amoeboid migratory switch // Biomedicines. 2021. Vol. 10, No. 1. P. 9. DOI: 10.3390/biomedicines10010009</mixed-citation></citation-alternatives></ref><ref id="B192"><label>192.</label><citation-alternatives><mixed-citation xml:lang="en">Zeng L, Kang C, Di C, et al. The adherens junction-associated protein 1 is a negative transcriptional regulator of MAGEA2, which potentiates temozolomide-induced apoptosis in GBM. Int J Oncol. 2014;44(4):1243–1251. DOI: 10.3892/ijo.2014.2277</mixed-citation><mixed-citation xml:lang="ru">Zeng L., Kang C., Di C. et al. The adherens junction-associated protein 1 is a negative transcriptional regulator of MAGEA2, which potentiates temozolomide-induced apoptosis in GBM // Int. J. Oncol. 2014. Vol. 44, No. 4. P. 1243–1251. DOI: 10.3892/ijo.2014.2277</mixed-citation></citation-alternatives></ref><ref id="B193"><label>193.</label><citation-alternatives><mixed-citation xml:lang="en">George J, Gondi CS, Dinh DH, et al. Restoration of tissue factor pathway inhibitor-2 in a human glioblastoma cell line triggers caspase-mediated pathway and apoptosis. Clin Cancer Res. 2007;13(12):3507–3517. DOI: 10.1158/1078-0432.CCR-06-3023</mixed-citation><mixed-citation xml:lang="ru">George J., Gondi C.S., Dinh D.H. et al. Restoration of tissue factor pathway inhibitor-2 in a human glioblastoma cell line triggers caspase-mediated pathway and apoptosis // Clin. Cancer Res. 2007. Vol. 13, No. 12. P. 3507–3517. DOI: 10.1158/1078-0432.CCR-06-3023</mixed-citation></citation-alternatives></ref><ref id="B194"><label>194.</label><citation-alternatives><mixed-citation xml:lang="en">El-Khayat SM, Arafat WO. Therapeutic strategies of recurrent glioblastoma and its molecular pathways ‘Lock up the beast’. Ecancermedicalscience. 2021;15:1176. DOI: 10.3332/ecancer.2021.1176</mixed-citation><mixed-citation xml:lang="ru">El-Khayat S.M., Arafat W.O. Therapeutic strategies of recurrent glioblastoma and its molecular pathways ‘Lock up the beast’ // Ecancermedicalscience. 2021. Vol. 15. P. 1176. DOI: 10.3332/ecancer.2021.1176</mixed-citation></citation-alternatives></ref><ref id="B195"><label>195.</label><citation-alternatives><mixed-citation xml:lang="en">Zheng Q, Han L, Dong Y, et al. JAK2/STAT3 targeted therapy suppresses tumor invasion via disruption of the EGFRvIII/JAK2/STAT3 axis and associated focal adhesion in EGFRvIII-expressing glioblastoma. Neuro Oncol. 2014;16(9):1229–1243. DOI: 10.1093/neuonc/nou046</mixed-citation><mixed-citation xml:lang="ru">Zheng Q., Han L., Dong Y. et al. JAK2/STAT3 targeted therapy suppresses tumor invasion via disruption of the EGFRvIII/JAK2/STAT3 axis and associated focal adhesion in EGFRvIII-expressing glioblastoma // Neuro. Oncol. 2014. Vol. 16, No. 9. P. 1229–1243. DOI: 10.1093/neuonc/nou046</mixed-citation></citation-alternatives></ref><ref id="B196"><label>196.</label><citation-alternatives><mixed-citation xml:lang="en">Tini P, Nardone V, Pastina P, et al. epidermal growth factor receptor expression predicts time and patterns of recurrence in patients with glioblastoma after radiotherapy and temozolomide. World Neurosurg. 2018;109:e662–e668. DOI: 10.1016/j.wneu.2017.10.052</mixed-citation><mixed-citation xml:lang="ru">Tini P., Nardone V., Pastina P. et al. epidermal growth factor receptor expression predicts time and patterns of recurrence in patients with glioblastoma after radiotherapy and temozolomide // World Neurosurg. 2018. Vol. 109. P. e662–e668. DOI: 10.1016/j.wneu.2017.10.052</mixed-citation></citation-alternatives></ref><ref id="B197"><label>197.</label><citation-alternatives><mixed-citation xml:lang="en">Hau P, Jachimczak P, Schlaier J, et al. TGF-β2 signaling in high-grade gliomas. Curr Pharm Biotechnol. 2011;12(12):2150–2157. DOI: 10.2174/138920111798808347</mixed-citation><mixed-citation xml:lang="ru">Hau P., Jachimczak P., Schlaier J. et al. TGF-β2 signaling in high-grade gliomas // Curr. Pharm. Biotechnol. 2011. Vol. 12, No. 12. P. 2150–2157. DOI: 10.2174/138920111798808347</mixed-citation></citation-alternatives></ref><ref id="B198"><label>198.</label><citation-alternatives><mixed-citation xml:lang="en">Gaetani P, Hulleman E, Levi D, et al. Expression of the transcription factor HEY1 in glioblastoma: a preliminary clinical study. Tumori. 2010;96(1):97–102.</mixed-citation><mixed-citation xml:lang="ru">Gaetani P., Hulleman E., Levi D. et al. Expression of the transcription factor HEY1 in glioblastoma: a preliminary clinical study // Tumori. 2010. Vol. 96, No. 1. P. 97–102.</mixed-citation></citation-alternatives></ref><ref id="B199"><label>199.</label><citation-alternatives><mixed-citation xml:lang="en">Shahi MH, Farheen S, Mariyath MPM, et al. Potential role of Shh-Gli1-BMI1 signaling pathway nexus in glioma chemoresistance. Tumour Biol. 2016;37(11):15107–15114. DOI: 10.1007/s13277-016-5365-7</mixed-citation><mixed-citation xml:lang="ru">Shahi M.H., Farheen S., Mariyath M.P.M. et al. Potential role of Shh-Gli1-BMI1 signaling pathway nexus in glioma chemoresistance // Tumour Biol. 2016. Vol. 37, No. 11. P. 15107–15114. DOI: 10.1007/s13277-016-5365-7</mixed-citation></citation-alternatives></ref><ref id="B200"><label>200.</label><citation-alternatives><mixed-citation xml:lang="en">Quail DF, Bowman RL, Akkari L, et al. The tumor microenvironment underlies acquired resistance to CSF1R inhibition in gliomas. Science. 2016;352(6288):aad3018. DOI: 10.1126/science.aad3018</mixed-citation><mixed-citation xml:lang="ru">Quail D.F., Bowman R.L., Akkari L. et al. The tumor microenvironment underlies acquired resistance to CSF1R inhibition in gliomas // Science. 2016. Vol. 352, No. 6288. P. aad3018. DOI: 10.1126/science.aad3018</mixed-citation></citation-alternatives></ref><ref id="B201"><label>201.</label><citation-alternatives><mixed-citation xml:lang="en">Koo C-Y, Muir KW, Lam E-F. FOXM1: from cancer initiation to progression and treatment. Biochim Biophys Acta. 2012;1819(1):28–37. DOI: 10.1016/j.bbagrm.2011.09.004</mixed-citation><mixed-citation xml:lang="ru">Koo C.-Y., Muir K.W., Lam E.W.F. FOXM1: from cancer initiation to progression and treatment // Biochim. Biophys. Acta. 2012. Vol. 1819, No. 1. P. 28–37. DOI: 10.1016/j.bbagrm.2011.09.004</mixed-citation></citation-alternatives></ref><ref id="B202"><label>202.</label><citation-alternatives><mixed-citation xml:lang="en">Wang Y, Wang X, Zhang J, et al. MicroRNAs involved in the EGFR/PTEN/AKT pathway in gliomas. J Neurooncol. 2012;106(2):217–224. DOI: 10.1007/s11060-011-0679-1</mixed-citation><mixed-citation xml:lang="ru">Wang Y., Wang X., Zhang J. et al. MicroRNAs involved in the EGFR/PTEN/AKT pathway in gliomas // J. Neurooncol. 2012. Vol. 106, No. 2. P. 217–224. DOI: 10.1007/s11060-011-0679-1</mixed-citation></citation-alternatives></ref><ref id="B203"><label>203.</label><citation-alternatives><mixed-citation xml:lang="en">Tian T, Mingyi M, Qiu X, Qiu Y. MicroRNA-101 reverses temozolomide resistance by inhibition of GSK3β in glioblastoma. Oncotarget. 2016;7(48):79584–79595. DOI: 10.18632/oncotarget.12861</mixed-citation><mixed-citation xml:lang="ru">Tian T., Mingyi M., Qiu X., Qiu Y. MicroRNA-101 reverses temozolomide resistance by inhibition of GSK3β in glioblastoma // Oncotarget. 2016. Vol. 7, No. 48. P. 79584–79595. DOI: 10.18632/oncotarget.12861</mixed-citation></citation-alternatives></ref><ref id="B204"><label>204.</label><citation-alternatives><mixed-citation xml:lang="en">Yue X, Lan F, Hu M, et al. Downregulation of serum microRNA-205 as a potential diagnostic and prognostic biomarker for human glioma. J Neurosurg. 2016;124(1):122–128. DOI: 10.3171/2015.1.JNS141577</mixed-citation><mixed-citation xml:lang="ru">Yue X., Lan F., Hu M. et al. Downregulation of serum microRNA-205 as a potential diagnostic and prognostic biomarker for human glioma // J. Neurosurg. 2016. Vol. 124, No. 1. P. 122–128. DOI: 10.3171/2015.1.JNS141577</mixed-citation></citation-alternatives></ref><ref id="B205"><label>205.</label><citation-alternatives><mixed-citation xml:lang="en">Huang H, Xiang Y, Su B, et al. Potential roles for Gfi1 in the pathogenesis and proliferation of glioma. Med Hypotheses. 2013;80(5):629–632. DOI: 10.1016/j.mehy.2013.02.007</mixed-citation><mixed-citation xml:lang="ru">Huang H., Xiang Y., Su B. et al. Potential roles for Gfi1 in the pathogenesis and proliferation of glioma // Med. Hypotheses. 2013. Vol. 80, No. 5. P. 629–632. DOI: 10.1016/j.mehy.2013.02.007</mixed-citation></citation-alternatives></ref><ref id="B206"><label>206.</label><citation-alternatives><mixed-citation xml:lang="en">Yao CJ, Han TY, Shih PH, et al. Elimination of cancer stem-like side population in human glioblastoma cells accompanied with stemness gene suppression by Korean herbal recipe MSC500. Integr Cancer Ther. 2014;13(6):541–554. DOI: 10.1177/1534735414549623</mixed-citation><mixed-citation xml:lang="ru">Yao C.J., Han T.Y., Shih P.H. et al. Elimination of cancer stem-like side population in human glioblastoma cells accompanied with stemness gene suppression by Korean herbal recipe MSC500 // Integr. Cancer Ther. 2014. Vol. 13, No. 6. P. 541–554. DOI: 10.1177/1534735414549623</mixed-citation></citation-alternatives></ref></ref-list></back></article>
