Oncotarget

Research Papers:

Downregulation of miR-199a-5p promotes prostate adeno-carcinoma progression through loss of its inhibition of HIF-1α

Jinjing Zhong, Rui Huang, Zhengzheng Su, Mengni Zhang, Miao Xu, Jing Gong, Ni Chen, Hao Zeng, Xueqin Chen _ and Qiao Zhou

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Oncotarget. 2017; 8:83523-83538. https://doi.org/10.18632/oncotarget.18315

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Abstract

Jinjing Zhong1, Rui Huang2, Zhengzheng Su1, Mengni Zhang1, Miao Xu1, Jing Gong1, Ni Chen1, Hao Zeng3, Xueqin Chen1 and Qiao Zhou1

1Department of Pathology, West China Hospital and National Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, China

2Department of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu 610041, China

3Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu 610041, Sichuan, China

Correspondence to:

Xueqin Chen, email: [email protected]

Qiao Zhou, email: [email protected]

Keywords: prostate cancer, microRNA, miR-199a-5p, HIF-1α

Received: February 08, 2017    Accepted: April 11, 2017    Published: May 31, 2017

ABSTRACT

Hypoxia-inducible factor-1 alpha (HIF-1α) plays key roles in cell survival under both hypoxia and normoxia conditions. Regulation of HIF-1α is complex and involves numerous molecules and pathways, including post-transcriptional regulation by microRNAs (miRNAs). Although upregulation of HIF-1α has been shown to promote prostate adenocarcinoma (PCa) progression, the mechanism by which miRNAs modulate HIF-1α in prostate cancer has not been clarified. Here, we show that miR-199a-5p is underexpressed in prostate adenocarcinoma. Artificial overexpression of miR-199a-5p decreased cell proliferation, motility, and tumor angiogenesis and increased apoptosis in PCa cell liness PC-3 and DU145 by directly targeting the 3’-untranslated region (UTR) of HIF-1α mRNA, which reduced HIF-1α levels as well as downstream genes transactivated by HIF-1α (such as VEGF, CXCR4, BNIP3 and BCL-xL). Abnormalities of miR-199a-HIF regulation may contribute significantly to PCa pathogenesis and progression.


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