期刊
FEBS LETTERS
卷 589, 期 1, 页码 102-109出版社
WILEY
DOI: 10.1016/j.febslet.2014.11.031
关键词
MicroRNA-520g; Hepatocellular carcinoma; Epithelial-mesenchymal transition; SMAD family member 7; Cancer metastasis
资金
- Natural Science Foundation of Guangdong Province [S2012020010942, 8151051501000029]
The aberrant expression of miR-520g is correlated with relapse, metastasis, and poor survival in hepatocellular carcinoma patients. It promotes HCC cell migration, invasion, and epithelial-mesenchymal transition (EMT) by targeting SMAD7.
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death worldwide. Aberrant expression of miRNAs contributes to HCC development. Here, we observed elevated miR-520g expression in tumor samples from HCC patients with relapse and metastasis, and this high miR-520g expression was correlated with poor survival. Through gain-and loss-of-function studies, miR-520g was demonstrated to facilitate HCC cell migration, invasion and epithelial-mesenchymal transition (EMT). SMAD7 was identified as a direct target of miR-520g. Accordingly, we conclude that high miR-520g expression promotes HCC cell mobility and EMT by targeting SMAD7, and this is correlated with reduced survival in HCC patients. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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