| Literature DB >> 28350134 |
Yongxiang Zhao1, Mingyu Yan2, Ye Yun1, Jianguo Zhang1, Ruimin Zhang1, Yan Li3, Xiangming Wu1, Qiang Liu1, Wei Miao1, Haishan Jiang1.
Abstract
MicroRNAs (miRNAs) are strongly implicated in various cancers, including prostate cancer. Recently, microRNA-455-3p (miR-455-3p) has been shown to be aberrantly expressed in many tumor tissues, but its functions in tumorigenesis remain unknown. In this study, we investigated the role of miR-455-3p in prostate cancer. We found that miR-455-3p is markedly downregulated in prostate cancer cell lines and clinical tumor specimens. Gain-of-function and loss-of-function studies showed that miR-455-3p promotes prostate cancer cell growth both in vitro and in vivo. Bioinformatics analysis and Luciferase reporter assays demonstrated that miR-455-3p directly targets and suppresses eIF4E, the rate-limiting factor for cap-dependent translation, which plays important roles in the initiation and progression of prostate cancers. Further studies demonstrated that miR-455-3p inhibits cap-dependent translation and the proliferation of prostate cancer cells through targeting eIF4E. Taken together, our findings suggest that miR-455-3p functions as a tumor suppressor by directly targeting eIF4E in prostate carcinogenesis and may be used as a potential target for therapeutic intervention in prostate cancer.Entities:
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Year: 2017 PMID: 28350134 DOI: 10.3892/or.2017.5502
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906