| Literature DB >> 31953872 |
Zhaohui Chen1, Likun Yang1, Liang Chen1, Jin Li2, Futian Zhang1, Yifei Xing1, Jun Zhao1.
Abstract
Bladder cancer is one of the most common urogenital malignancies. However, its pathogenesis, especially molecular mechanisms remain elusive. Thus, understanding the molecular mechanisms underlying bladder cancer is important for the discovery of novel therapeutic paradigms for these diseases. In current study, we found that micro-RNA (miR)-190b is highly expressed in bladder cancer tissues and cells. Overexpression of miR-190b enhanced the proliferation, growth, migration and invasion capabilities, and angiogenesis of bladder cancer cells, whereas downregulation of miR-190b reversed these effects. Target prediction and dual luciferase reporter assays identified NLR family CARD domain containing 3 (NLRC3) as a potential target of miR-190b. Pathway analysis indicated that miR-190b promotes bladder cancer progression via the Wnt/β-catenin and mTOR signaling pathways. Taken together, our findings imply that miR-190b acts as a critical regulator for bladder cancer development by repressing NLRC3 and partly through the Wnt/β-catenin and mTOR pathways. Our study suggests that miR-190b may be served as a potential therapeutic target for bladder cancer treatment.Entities:
Keywords: NLRC3 expression; Wnt/β-catenin and mTOR signaling; bladder cancer; micro-RNA
Year: 2020 PMID: 31953872 DOI: 10.1096/fj.201901764R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191