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MicroRNA-455-3p functions as a tumor suppressor by targeting eIF4E in prostate cancer
Author(s) -
Yongxiang Zhao,
Mingyu Yan,
Yun Ye,
JianGuo Zhang,
Ruimin Zhang,
Yan Li,
Xiangming Wu,
Qiang Liu,
Wei Miao,
Haishan Jiang
Publication year - 2017
Publication title -
oncology reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.094
H-Index - 96
eISSN - 1791-2431
pISSN - 1021-335X
DOI - 10.3892/or.2017.5502
Subject(s) - prostate cancer , carcinogenesis , cancer research , oncogene , microrna , cancer , prostate , biology , eif4e , cell cycle , oncology , medicine , translation (biology) , messenger rna , gene , biochemistry
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.

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