| Literature DB >> 31975504 |
Cong Wang1, Motohide Uemura1,2, Eisuke Tomiyama1, Makoto Matsushita1, Yoko Koh1, Kosuke Nakano1, Yujiro Hayashi1, Yu Ishizuya1, Kentaro Jingushi3, Taigo Kato1,2, Koji Hatano1, Atsunari Kawashima1, Takeshi Ujike1, Akira Nagahara1, Kazutoshi Fujita1, Ryoichi Imamura1, Kazutake Tsujikawa3, Norio Nonomura1.
Abstract
Although several studies have reported that microRNA (miR)-92b-3p is involved in various cellular processes related to carcinogenesis, its physiological role in clear cell renal cell carcinoma (ccRCC) remains unclear. To clarify the role of miR-92b-3p in ccRCC, we compared miR-92b-3p expression levels in ccRCC tissues and adjacent normal renal tissues. Significant upregulation of miR-92b-3p was observed in ccRCC tissues. Overexpression of miR-92b-3p using a miRNA mimic promoted proliferation, migration, and invasion activities of ACHN cells. Functional inhibition of miR-92b-3p by a hairpin miRNA inhibitor suppressed Caki-2 cell growth and invasion activities in vitro. Mechanistically, it was found that miR-92b-3p directly targeted the TSC1 gene, a known upstream regulator of mTOR. Overexpression of miR-92b-3p decreased the protein expression of TSC1 and enhanced the downstream phosphorylation of p70S6 kinase, suggesting that the mTOR signaling pathway was activated by miR-92b-3p in RCC cells. Importantly, a multivariate Cox proportion hazard model, based on TNM staging and high levels of miR-92b-3p, revealed that miR-92b-3p expression (high vs. low hazard ratio, 2.86; 95% confidence interval, 1.20-6.83; P = .018) was a significant prognostic factor for overall survival of ccRCC patients with surgical management. Taken together, miR-92b-3p was found to act as an oncomiR, promoting cell proliferation by downregulating TSC1 in ccRCC.Entities:
Keywords: TSC1; ccRCC; miR-92b-3p; oncomiR; proliferation
Year: 2020 PMID: 31975504 DOI: 10.1111/cas.14325
Source DB: PubMed Journal: Cancer Sci ISSN: 1347-9032 Impact factor: 6.716