Department of Urology, Shanghai Tenth People's Hospital, School of Medicine in Tongji University, 301 Yanchang Road, Jing'an District, Shanghai 200072, China.
Biomed Res Int. 2021 Jul 7;2021:9950749. doi: 10.1155/2021/9950749. eCollection 2021.
The role of miRNAs in renal cell carcinoma (RCC) is not certain. We wanted to study the biological functions and potential mechanisms of miR-101-3p in RCC.
miR-101-3p was inhibited in A498 and OSRC-2 (two RCC cell lines). We studied its effect on cell invasion and proliferation. Target EZH2 of miR-101-3p was designated by different methods, including luciferase functional analysis and Western blotting. The expression level of the target gene in treated cells was quantitatively analyzed by quantitative real-time polymerase chain reaction. In addition, induction of miR-101-3p to prevent tumor formation of A498 cells in mice was further studied.
The overexpression of miR-101-3p significantly inhibited the proliferation, migration, and invasion in two RCC cells. Western blotting and luciferase functional analysis indicated that miR-101-3p regulated the expression of EZH2 in two cell lines. Mice inoculated with A498 and OSRC-2 cells transfected with miR-101-3p mimics showed significantly smaller xenografts and weaker EZH2 expression levels than the control group.
miR-101-3p inhibited RCC cell proliferation, migration, and invasion by targeting EZH2.
miRNAs 在肾细胞癌(RCC)中的作用尚不确定。我们希望研究 miR-101-3p 在 RCC 中的生物学功能和潜在机制。
在 A498 和 OSRC-2(两种 RCC 细胞系)中抑制 miR-101-3p。我们研究了它对细胞侵袭和增殖的影响。通过不同的方法确定 miR-101-3p 的靶基因 EZH2,包括荧光素酶功能分析和 Western blot。通过定量实时聚合酶链反应定量分析处理细胞中靶基因的表达水平。此外,进一步研究了 miR-101-3p 诱导 A498 细胞肿瘤形成的能力。
miR-101-3p 的过表达显著抑制了两种 RCC 细胞的增殖、迁移和侵袭。Western blot 和荧光素酶功能分析表明,miR-101-3p 调节两种细胞系中 EZH2 的表达。与对照组相比,接种 miR-101-3p 模拟物转染的 A498 和 OSRC-2 细胞的小鼠异种移植物明显较小,EZH2 表达水平较弱。
miR-101-3p 通过靶向 EZH2 抑制 RCC 细胞的增殖、迁移和侵袭。