Changes in protein expression of rat astrocytes co-cultured with C6 glioma cells


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Introduction. Based on current literature data, it is possible to assume that when exposed to glioma cells astrocytes, may undergo a reactive transformation. These glioma-conditioned astrocytes might create a permissive environment for tumorigenesis. The aim of the study. To investigate the effects of glioma cells on astrocytes in co-culture. Methods. In terms of the current work, we conducted a pairwise comparison of protein levels between C6 glioma cells, native rat astrocytes, and glioma-conditioned rat astrocytes. The samples were prepared and analyzed with liquid chromatography-high-resolution mass spectrometry. Results. The analysis showed a significant difference in 162 proteins between glioma cells and native astrocytes, in 141 proteins between glioma cells and glioma-conditioned astrocytes and 70 proteins between glioma-conditioned and native astrocytes. Conclusion. The differences in protein levels between native and glioma-conditioned astrocytes show a high correlation with differences between glioma cells and native astrocytes.

Full Text

Restricted Access

About the authors

A. S Silantyev

National Scientific Research Center on Addictions a branch of the V.P. Serbsky National Medical Research Centre for Psychiatry and Narcology

Maly Mogiltsevsky by-streeT., 3, Moscow, 119002, Russian Federation

I. V Chekhonin

V.P. Serbsky National Medical Research Centre for Psychiatry and Narcology

Kropotkinskiy by-streeT., 23, Moscow, 119034, Russian Federation

A. A Chernysheva

V.P. Serbsky National Medical Research Centre for Psychiatry and Narcology

Email: aachernysheva512@gmail.com
Kropotkinskiy by-streeT., 23, Moscow, 119034, Russian Federation

O. I Gurina

V.P. Serbsky National Medical Research Centre for Psychiatry and Narcology

Kropotkinskiy by-streeT., 23, Moscow, 119034, Russian Federation

S. A Pavlova

Institute of Gene Biology Russian Academy of Sciences

Vavilova StreeT., 34/5, Moscow, 119334, Russian Federation

G. V Pavlova

Institute of Gene Biology Russian Academy of Sciences; Sechenov First Moscow State Medical University; N.N. Burdenko National Medical Research Center of Neurosurgery

Institute of Molecular Medicine Vavilova StreeT., 34/5, Moscow, 119334, Russian Federation; Trubetskaya StreeT., 8, Moscow, 119991, Russian Federation; 4 Tverskaya-Yamskaya str., 16, Moscow, 125047, Russian Federation

T. A Savelieva

Prokhorov General Physics Institute; National Research Nuclear University

Moscow Engineering Physics Institute Vavilova str., 38, Moscow, 119991, Russian Federation; Kashirskoe Highway, 31, Moscow, 115409, Russian Federation

V. B Loshhenov

Prokhorov General Physics Institute; National Research Nuclear University

Moscow Engineering Physics Institute Vavilova str., 38, Moscow, 119991, Russian Federation; Kashirskoe Highway, 31, Moscow, 115409, Russian Federation

V. P Chekhonin

V.P. Serbsky National Medical Research Centre for Psychiatry and Narcology; Pirogov Russian National Research Medical University

Kropotkinskiy by-streeT., 23, Moscow, 119034, Russian Federation; Ostrovitianova str., 1, Moscow, 117997, Russian Federation

References

  1. Charles N.A., Holland E.C., Gilbertson R., Glass R., Kettenmann H. The brain tumor microenvironment. Glia. 2012; 60 (3): 502-14. https://doi.org/10.1002/glia.21264
  2. Zamanian J.L., Xu L., Foo L.C., Nouri N., Zhou L., Giffard R.G., Barres B.A. Genomic analysis of reactive astrogliosis. J. Neurosci. 2012; 32 (18): 6391-410. https://doi.org/10.1523/jneuro-sci.6221-11.2012
  3. Placone A.L., Quinones-Hinojosa A., Searson P.C. The role of astrocytes in the progression of brain cancer: complicating the picture of the tumor microenvironment. Tumour Biol. 2015. https://doi.org/10.1007/s13277-015-4242-0
  4. Lu P., Wang Y., Liu X., Wang H., Zhang X., Wang K., Wang Q.,Hu R. Malignant gliomas induce and exploit astrocytic mesenchymal-like transition by activating canonical Wnt/beta-catenin signaling. Med Oncol. 2016; 33 (7): 66. https://doi.org/10.1007/s12032-016-0778-0
  5. Biasoli D., Sobrinho M.F., da Fonseca A.C., de Matos D.G., Romao L., de Moraes Maciel R., Rehen S.K., Moura-Neto V., Borges H.L.,Lima FR. Glioblastoma cells inhibit astrocytic p53-expression favoring cancer malignancy. Oncogenesis. 2014; 3: 123. https://doi org/10.1038/oncsis.2014.36
  6. Baklaushev V.P., Yusubalieva G.M., Tsitrin E.B., Gurina O.I., Grinenko N.P., Victorov I.V., Chekhonin V.P Visualization of Connexin 43-positive cells of glioma and the periglioma zone by means of intravenously injected monoclonal antibodies. Drug Deliv. 2011; 18 (5): 331-7. https://doi.org/10.3109/10717544.20 10.549527
  7. Suk K. Proteomic analysis of glioma chemoresistance. Curr Neuropharmacol. 2012; 10 (1): 72-9. https://doi.org/10.2174/157015912799362733
  8. Deighton R.F., McGregor R., Kemp J., McCulloch J., Whittle I.R. Glioma pathophysiology: insights emerging from proteomics. Brain Pathol. 2010; 20 (4): 691-703. https://doi.org/10.1111/j.1750-3639.2010.00376.x
  9. Koncarevic S., Urig S., Steiner K., Rahlfs S., Herold-Mende C., Sueltmann H., Becker K. Differential genomic and proteomic profiling of glioblastoma cells exposed to terpyridineplatinum (II) complexes. Free Radic Biol Med. 2009; 46 (8): 1096-108. https://doi.org/10.1016/j.freeradbiomed.2009.01.013
  10. Khalil A.A. Biomarker discovery: a proteomic approach for brain cancer profiling. Cancer Sci. 2007; 98 (2): 201-13. https://doi.org/10.1111/j.1349-7006.2007.00374.x
  11. Han M.Z., Xu R., Xu Y.Y., Zhang X., Ni S.L., Huang B., Chen A.J., Wei Y.Z., Wang S., Li W.J., Zhang Q., Li G., Li X.G., Wang J. TAGLN2 is a candidate prognostic biomarker promoting tumorigenesis in human gliomas. J. Exp. Clin. Cancer Res. 2017; 36 (1): 155. https://doi.org/10.1186/ s13046-017-0619-9
  12. Stifani S. The Multiple Roles of Peptidyl Prolyl Isomerases in Brain Cancer. Biomolecules. 2018; 8 (4). https://doi.org/10.3390/biom8040112

Supplementary files

Supplementary Files
Action
1. JATS XML

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies