电邮这篇文章 Methylation of the genes for the microRNAs miR-129-2 and miR-9-1, changes in their expression, and activation of their potential target genes in clear cell renal cell carcinoma
- 作者: Pronina I.V.1,2, Klimov E.A.3, Burdennyy A.M.2,4, Beresneva E.V.5, Fridman M.V.6, Ermilova V.D.7, Kazubskaya T.P.7, Karpukhin A.V.1, Braga E.A.1,2, Loginov V.I.1,2
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隶属关系:
- Research Centre of Medical Genetics
- Institute of General Pathology and Pathophysiology
- Biological Faculty, Moscow State University
- Emanuel Institute of Biochemical Physics
- State Research Institute of Genetics and Selection of Industrial Microorganisms
- Vavilov Institute of General Genetics
- Cancer Research Center
- 期: 卷 51, 编号 1 (2017)
- 页面: 61-71
- 栏目: Molecular Cell Biology
- URL: https://journals.rcsi.science/0026-8933/article/view/162931
- DOI: https://doi.org/10.1134/S0026893316060169
- ID: 162931
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详细
Methylation of promoter CpG islands and microRNA (miRNA) interactions with mRNAs of target genes are epigenetic mechanisms that play a crucial role in deregulation of gene expression and signaling pathways in tumors. Altered expression of six chromosome 3p genes (RARB(2), SEMA3B, RHOA, GPX1, NKIRAS1, and CHL1) and two miRNA genes (MIR-129-2 and MIR-9-1) was observed in primary clear cell renal cell carcinomas (ccRCCs, 31–48 samples) by RT-PCR and qPCR. Significant downregulation (p < 0.05, Fisher’s exact test) was observed for SEMA3B, NKIRAS1, and CHL1; and differential expression, for the other chromosome 3p and miRNA genes. Methylation-specific PCR with primers to RARB(2), SEMA3B, MIR-129-2, and MIR-9-1 showed that their methylation frequency was significantly (p < 0.05, Fisher’s exact test) elevated in the ccRCC samples. Significant correlations between promoter methylation and expression were confirmed for SEMA3B and observed for the first time for RARB(2), GPX1, and MIR-129-2 in ccRCC (Spearman’s correlation coefficient rs ranging 0.31–0.60, p < 0.05). The MIR-129-2 and RARB(2) methylation frequencies significantly correlated with ccRCC progression. MIR-129-2 methylation correlated with upregulation of RARB(2), RHOA, NKIRAS1, and CHL1 (rs ranging 0.35–0.53, p < 0.05). The findings implicate methylation in regulating RARB(2), SEMA3B, GPX1, and MIR-129-2 and indicate that miR-129-2 and methylation of its gene affect RARB(2), RHOA, NKIRAS1, and CHL1 expression.
作者简介
I. Pronina
Research Centre of Medical Genetics; Institute of General Pathology and Pathophysiology
编辑信件的主要联系方式.
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 115478; Moscow, 125315
E. Klimov
Biological Faculty, Moscow State University
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 119234
A. Burdennyy
Institute of General Pathology and Pathophysiology; Emanuel Institute of Biochemical Physics
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 125315; Moscow, 119334
E. Beresneva
State Research Institute of Genetics and Selection of Industrial Microorganisms
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 117545
M. Fridman
Vavilov Institute of General Genetics
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 117971
V. Ermilova
Cancer Research Center
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 115478
T. Kazubskaya
Cancer Research Center
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 115478
A. Karpukhin
Research Centre of Medical Genetics
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 115478
E. Braga
Research Centre of Medical Genetics; Institute of General Pathology and Pathophysiology
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 115478; Moscow, 125315
V. Loginov
Research Centre of Medical Genetics; Institute of General Pathology and Pathophysiology
Email: zolly_sten@mail.ru
俄罗斯联邦, Moscow, 115478; Moscow, 125315
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