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miR-101-3p Serves as a Tumor Suppressor for Renal Cell Carcinoma and Inhibits Its Invasion and Metastasis by Targeting EZH2
Author(s) -
Yunze Dong,
Yuchen Gao,
Tiancheng Xie,
Huan Liu,
Xiangcheng Zhan,
Yunfei Xu
Publication year - 2021
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2021/9950749
Subject(s) - blot , microrna , ezh2 , cell culture , cell growth , transfection , cancer research , metastasis , renal cell carcinoma , biology , luciferase , cell , suppressor , nasopharyngeal carcinoma , microbiology and biotechnology , gene expression , medicine , cancer , pathology , gene , genetics , radiation therapy
Background 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.Methods 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.Results 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.Conclusions miR-101-3p inhibited RCC cell proliferation, migration, and invasion by targeting EZH2.

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