Zhong Jinjing, Huang Rui, Su Zhengzheng, Zhang Mengni, Xu Miao, Gong Jing, Chen Ni, Zeng Hao, Chen Xueqin, Zhou Qiao
Department of Pathology, West China Hospital and National Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, China.
Department of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu 610041, China.
Oncotarget. 2017 May 31;8(48):83523-83538. doi: 10.18632/oncotarget.18315. eCollection 2017 Oct 13.
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.
缺氧诱导因子-1α(HIF-1α)在缺氧和常氧条件下的细胞存活中发挥关键作用。HIF-1α的调控较为复杂,涉及众多分子和信号通路,包括微小RNA(miRNA)的转录后调控。虽然已有研究表明HIF-1α的上调会促进前列腺腺癌(PCa)进展,但miRNA在前列腺癌中调节HIF-1α的机制尚未阐明。在此,我们发现miR-199a-5p在前列腺腺癌中表达下调。通过直接靶向HIF-1α mRNA的3'-非翻译区(UTR),人工过表达miR-199a-5p可降低PC-3和DU145前列腺癌细胞系的细胞增殖、迁移能力以及肿瘤血管生成,并增加细胞凋亡,这降低了HIF-1α水平以及由HIF-1α反式激活的下游基因(如VEGF、CXCR4、BNIP3和BCL-xL)的表达。miR-199a-HIF调控异常可能在很大程度上促成了PCa的发病机制和进展。