| Literature DB >> 23352645 |
Bisheng Zhou1, Ruihua Ma, Wenxia Si, Sisi Li, Yan Xu, Xin Tu, Qing Wang.
Abstract
FGF2 and VEGFA are the two most potent angiogenic factors. Here we report that miR-503 can simultaneously down-regulate FGF2 and VEGFA. The expression of miR-503 is repressed in HCC cells and primary tumors due to a potential epigenetic mechanism. Overexpression of miR-503 reduced tumor angiogenesis in vitro and in vivo. We also found that miR-503 expression was down-regulated by hypoxia through HIF1α. These results identify a miRNA that targets both FGF2 and VEGFA in cancers, demonstrate the anti-angiogenesis role of miR-503 in tumorigenesis, and provide a novel mechanism for hypoxia-induced FGF2 and VEGFA through HIF1α-mediated inhibition of miR-503. Published by Elsevier Ireland Ltd.Entities:
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Year: 2013 PMID: 23352645 DOI: 10.1016/j.canlet.2013.01.028
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679