Clinical significance of methylation of lncRNA genes GAS5, ZEB1-AS1 in tumors of patients with breast cancer
- Authors: Osipova A.A.1, Ryabchikov D.A.2, Chulkova S.V.2,3, Loginov V.I.4, Burdennyy A.M.4, Kushlinskii N.E.1,2
-
Affiliations:
- Russian University of Medicine Ministry of Health of Russia
- N.N. Blokhin National Medical Research Center of Oncology Ministry of Health of Russian Federation
- I.I. Pirogov Russian Research Medical University
- Research Institute of General Pathology and Pathophysiology
- Issue: Vol 28, No 11 (2025)
- Pages: 59-67
- Section: Medical chemistry
- URL: https://journals.eco-vector.com/1560-9596/article/view/696262
- DOI: https://doi.org/10.29296/25877313-2025-11-08
- ID: 696262
Cite item
Abstract
Introduction. Long non-coding RNAs (LncRNAs) are transcripts whose role in carcinogenesis is poorly understood. LncRNA expression determines the biological properties of a cell, including invasive potential and ability to migrate. Methylation status changes lncRNA functions and can be a marker of tumor prognosis.
The aim of the work is study the methylation frequency of the LncRNA genes GAS5, ZEB1-AS1 in breast cancer and to evaluate the clinical significance.
Material and methods. 140 patients with breast cancer were examined, mainly with T1 – (38.7%) and T2 – (55.6%) stages, N0 status – (54.0%), N1 status – (37.9%). Luminal type of breast cancer – 80% (n = 113), non-luminal – 20% (n = 27). Morphologically: invasive ductal carcinoma (77.1%), G2 differentiation (62.9%) were predominantly detected. Methylation of CpG regions of promoter regions of the GAS5, ZEB1-AS1 lncRNAs genes in paired tumor and histologically unaffected breast tissue samples was studied using the methyl-specific PCR method. The T100 amplifier (Bio-Rad, USA) and Lasergene 17.1 primers from DNASTAR (USA) were used in the work. Statistical data processing was performed in the SPSS, v. 23 program.
Results. The frequency of methylation of the GAS5, ZEB1-AS1 genes in the tumor is higher than in histologically unaffected breast tissue. Gene methylation is associated with age, R = 0.43 (GAS5) and R = 0.26 (ZEB1-AS1), and increases the stage tumor process. A correlation was established between GAS5 gene methylation and the T index (R = 0.21, p < 0.05), N status (R = 0.31, p < 0.05). There is an inverse correlation with the biological subtype of luminal cancer (R = –0.29, p < 0.05). The absence of methylation of the GAS5 and ZEB1-AS1 genes is associated with a decrease in 5-year overall survival and 10-year progression-free survival in breast cancer.
Conclusions. In breast cancer, methylation of the lncRNAs GAS5, ZEB1-AS1 genes in the tumor exceeds that in the unchanged breast tissue. The methylation status of the genes GAS5, ZEB1-AS1 is associated with the stage, tumor size, regional metastasis, and does not affect the long-term treatment results.
Keywords
Full Text
About the authors
A. A. Osipova
Russian University of Medicine Ministry of Health of Russia
Author for correspondence.
Email: osipova_ronc@mail.ru
ORCID iD: 0009-0003-3046-9117
SPIN-code: 1068-1015
Post-graduate Student, Department of Oncology
Russian Federation, 4 Dolgorukovskaya, Moscow, 127006D. A. Ryabchikov
N.N. Blokhin National Medical Research Center of Oncology Ministry of Health of Russian Federation
Email: dr.denisr@mail.ru
ORCID iD: 0000-0003-2670-2361
SPIN-code: 9328-9425
Dr.Sc. (Med.), Head of the Department of Abdominal Oncology
Russian Federation, 24 Kashirskoe shosse, Moscow, 115522S. V. Chulkova
N.N. Blokhin National Medical Research Center of Oncology Ministry of Health of Russian Federation; I.I. Pirogov Russian Research Medical University
Email: chulkova@mail.ru
ORCID iD: 0000-0003-4412-5019
SPIN-code: 1676-2156
Dr.Sc. (Med.), Senior Research Scientist, Laboratory of Clinical Immunology and Innovative Technologies, Assistant Professor, Department of Oncology and Radiotherapy
Russian Federation, 24 Kashirskoe shosse, Moscow, 115522; 1a Ostrovityanova, Moscow, 117997V. I. Loginov
Research Institute of General Pathology and Pathophysiology
Email: loginov7w@gmail.com
ORCID iD: 0000-0003-2668-8096
SPIN-code: 6249-5883
Ph.D. (Biol.), Leading Research Scientist, Laboratory of Pathogenomics and Transcriptomics
Russian Federation, 8 Baltiyskaya, Moscow, 125315A. M. Burdennyy
Research Institute of General Pathology and Pathophysiology
Email: burdennyy@gmail.com
ORCID iD: 0000-0002-9398-8075
SPIN-code: 4429-4288
Ph.D. (Biol.), Leading Research Scientist, Laboratory of Pathogenomics and Transcriptomics
Russian Federation, 8 Baltiyskaya, Moscow, 125315N. E. Kushlinskii
Russian University of Medicine Ministry of Health of Russia; N.N. Blokhin National Medical Research Center of Oncology Ministry of Health of Russian Federation
Email: biochimia@yandex.ru
ORCID iD: 0000-0002-3898-4127
SPIN-code: 6225-1487
Dr.Sc. (Med.), Professor, Member of RAS, Head of the Department of Clinical Biochemistry, Scientific Head of Clinical Diagnostic Laboratory
Russian Federation, 4 Dolgorukovskaya, Moscow, 127006; 24 Kashirskoe shosse, Moscow, 115522References
- Bray F., Ferlay J., Soerjomataram I. et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2018; 68: 394–424. doi: 10.3322/caac.21492.
- Sung H., Ferlay J., Siegel R.L. et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021; 71(3): 209-249. doi: 10.3322/caac.21660.
- Esteva F.J., Hubbard-Lucey V.M., Tang J. et al. Immunotherapy and targeted therapy combinations in metastatic breast cancer. Lancet Oncol. 2019; 20: e175–186. doi: 10.1016/S1470-2045(19)30026-9.
- Liu B., Fan Y., Song Z. et al. Identification of DRP1 as a prognostic factor correlated with immune infiltration in breast cancer. Int Immunopharmacol. 2020; 89: 107078. doi: 10.1016/j.intimp.2020.107078.
- Ryabchikov D.A., Abdullaeva E.I., Dudina I.A. i dr. The role of microRNA in carcinogenesis and prognosis of malignant neoplasms of the mammary gland. Vestnik of the Russian Scientific Center of Roentgenoradiology. 2018; 18(2): 5. (In Russ.).
- Sinn B.V., Weber K.E., Schmitt W.D. et al. Human leucocyte antigen class I in hormone receptor-positive, HER2-negative breast cancer: association with response and survival after neoadjuvant chemotherapy. Breast Cancer Res. 2019; 21: 142. doi: 10.1186/s13058-019-1231-z.
- Ryabchikov D.A., Beznos O.A., Dudina I.A. i dr. Disseminated tumor cells in patients with luminal breast cancer. Russian Journal of Biotherapy. 2018; 17(1): 53–57. (In Russ.). doi: 10.17650/1726-9784-2018-17-1-53-57.
- Titov K.S., Kazakov A.M., Baryshnikova M.A. i dr. Some molecular and immunological prognostic factors of triple-negative breast cancer. Oncogynecology. 2019; 4(32): 26–34. (In Russ.). doi: 10.52313/22278710_2019_4_26.
- Talipov O.A., Ryabchikov D.A., Chulkova S.V. i dr. Methylation of suppressor microRNA genes in breast cancer. Oncogynecology. 2020; 2(34): 14–22. (In Russ.). doi: 10.52313/22278710_2020_2_14.
- Afroze N., Sundaram M.K., Haque S., Hussain A. Long non-coding RNA involved in the carcinogenesis of human female cancer – a comprehensive review. Discov. Oncol. 2025; 16(1): 122. doi: 10.1007/s12672-025-01848-1.
- Tordonato C., Di Fiore P.P., Nicassio F. The role of non-coding RNAs in the regulation of stem cells and progenitors in the normal mammary gland and in breast tumors. Front Genet. 2015; 6: 72. doi: 10.3389/fgene.2015.00072.
- Arun G., Diermeier S., Akerman M. et al. Differentiation of mammary tumors and reduction in metastasis upon Malat1 lncRNA loss. Genes Dev. 2016; 30(1):34-51. DOI: doi: 10.1101/gad.270959.115.
- Song J., Cui Q., Gao J. Roles of lncRNAs related to the p53 network in breast cancer progression. Front Oncol. 2024; 14: 1453807. doi: 10.3389/fonc.2024.1453807.
- Selezneva Al.D., Lukina S.S., Pronina I.V. i dr. Сhanges in methylation of a group of apoptosis-associated protein-coding genes and long non-coding RNA genes as a factor of dysregulation of their expression in breast cancer. Pathological physiology and experimental therapy. 2024; 68(4): 4–13. (In Russ.). doi: 10.25557/0031-2991.2024.04.4-13.
- Solaimani M., Hosseinzadeh S., Abasi M. Non-coding RNAs, a double-edged sword in breast cancer prognosis. Cancer Cell Int. 2025; 25(1):123. doi: 10.1186/s12935-025-03679-0.
- Zhang Y., Yan H., Jiang Y. et al. Long non-coding RNA IGF2-AS represses breast cancer tumorigenesis by epigenetically regulating IGF2. Exp. Biol. Med. (Maywood). 2021; 246(4): 371–379. doi: 10.1177/1535370220966253.
- Chen C., Feng Y., Wang X. LncRNA ZEB1-AS1 expression in cancer prognosis: Review and meta-analysis. Clin. Chim. Acta. 2018; 484: 265–271. doi: 10.1016/j.cca.2018.06.007.
- Hu G., Lou Z., Gupta M. The long non-coding RNA GAS5 cooperates with the eukaryotic translation initiation factor 4E to regulate c-Myc translation. PloS ONE. 2014; 9(9): e107016. doi: 10.1371/journal.pone.0107016.
- Burdenny A.M., Filippova E.A., Ivanova N.A. i dr. Hypermethylation of genes encoding new long noncoding RNAs in ovarian tumors and metastases: a dual effect. Bulletin of Experimental Biology and Medicine. 2021; 171(3): 353–358 (In Russ.).
- Liu X.J., Li S.L., Li J.S. et al. Long non-coding RNA ZEB1-AS1 is associated with poor prognosis in gastric cancer and promotes cancer cell metastasis. Eur. Rev. Med. Pharmacol. Sci. 2018; 22(9): 2624–2630. doi: 10.26355/eurrev_201805_14956.
- Brierley J.D., Gospodarowicz M.K., Wittekind C. eds. Union for International Cancer Control (UICC). TNM Classification of Malignant Tumours, 8th edn. Chichester, West Sussex, UK; Hoboken, NJ: John Wiley & Sons, 2017.
- Loginov V.I., Khodyrev D.S., Pronina I.V. et al. Methylation of the promoter region of the RASSF1A gene and the frequency of allelic imbalances in critical regions of chromosome 3 correlate with the progression of clear cell renal cell carcinoma. Molecular biology. 2009; 43(3): 429–438. (In Russ.).
Supplementary files




