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MiR-338-3p targets RAB23 and suppresses tumorigenicity of prostate cancer cells.


ABSTRACT: MicroRNA-338-3p (miR-338-3p) has been implicated in several cancers; however, its role in human prostate cancer remains unknown. In this study, we observed downregulation of miR-338-3p in prostate cancer tissues and cell lines. Forced expression of miR-338-3p suppressed prostate cancer cell proliferation, migration, and invasion in vitro and tumor growth in vivo, while apoptosis was induced. Further experiments revealed that RAB23 is a target of miR-338-3p because miR-338-3p bound directly to the 3'-untranslated region (3'-UTR) of RAB23 mRNA, thereby reducing both the mRNA and protein levels of RAB23. Reintroduction of RAB23 attenuated the inhibitory effects of miR-338-3p on proliferation, migration, and invasiveness of prostate cancer cells. In clinical samples, miR-338-3p levels negatively correlated with RAB23 expression, which was upregulated in prostate cancer. Collectively, these results indicate that miR-338-3p acts as a tumor suppressor in prostate cancer by directly targeting RAB23.

SUBMITTER: Wang Y 

PROVIDER: S-EPMC6325485 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

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miR-338-3p targets <i>RAB23</i> and suppresses tumorigenicity of prostate cancer cells.

Wang Yuxiong Y   Qin Haiyan H  

American journal of cancer research 20181201 12


MicroRNA-338-3p (miR-338-3p) has been implicated in several cancers; however, its role in human prostate cancer remains unknown. In this study, we observed downregulation of miR-338-3p in prostate cancer tissues and cell lines. Forced expression of miR-338-3p suppressed prostate cancer cell proliferation, migration, and invasion <i>in vitro</i> and tumor growth <i>in vivo</i>, while apoptosis was induced. Further experiments revealed that <i>RAB23</i> is a target of miR-338-3p because miR-338-3p  ...[more]

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