Hepatitis C virus represses E-cadherin expression via DNA methylation to induce epithelial to mesenchymal transition in human hepatocytes

被引:19
|
作者
Park, Jungmi [1 ]
Jang, Kyung Lib [1 ]
机构
[1] Pusan Natl Univ, Coll Nat Sci, Dept Microbiol, Pusan 609735, South Korea
基金
新加坡国家研究基金会;
关键词
DNA methylation; E-cadherin; Hepatitis C virus; Epithelial-mesenchymal transition; TUMOR-SUPPRESSOR GENES; CELL-CELL ADHESION; X PROTEIN; ACTIVATION; PROMOTER; SYSTEM; GROWTH; HYPERMETHYLATION; INFECTION;
D O I
10.1016/j.bbrc.2014.03.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis C virus (HCV) core protein is known to induce promoter hypermethylation of tumor suppressor genes including E-cadherin to repress their expression when overexpressed in human hepatocytes; however, its actual role during HCV infection is still unknown. Here, we report that infection with HCV derived from pJFH-1 replicon system that mimics natural infection elevates protein levels of DNA methyltransferase 1 and 3b to enhance DNMT activity in human hepatocytes. As a consequence, HCV induced promoter hypermethylation of E-cadherin, resulting in repression of its expression. In addition down-regulation of E-cadherin by HCV led to epithelial-mesenchymal transition that is known to be a critical event during the late stage of tumorigenesis. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:561 / 567
页数:7
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