Overexpression of hepatitis C virus NS5A protein induces chromosome instability via mitotic cell cycle dysregulation

被引:34
作者
Baek, Kwan-Hyuck
Park, Hye-Young
Kang, Chang-Mo
Kim, So-Jung
Jeong, Sook-Jung
Hong, Eun-Kyung
Park, Joong-Won
Sung, Young-Chul
Suzuki, Tetsuro
Kim, Chang-Min
Lee, Chang-Woo [1 ]
机构
[1] Natl Canc Ctr, Inst Res, Goyang 411764, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Biomed Res Inst, Ctr Mol Med,Dept Mol Cell Biol, Suwon 440746, South Korea
[3] Korea Inst Radiol & Med Sci, Seoul 139706, South Korea
[4] Pohang Univ Sci & Technol, POSTECH Biotech Ctr, Div Mol & Life Sci, Pohang 790784, South Korea
[5] Natl Inst Infect Dis, Tokyo 1628640, Japan
关键词
hepatitis C virus; NS5A; mitotic cell cycle; chromosome instability; hepatocellular carcinoma;
D O I
10.1016/j.jmb.2006.03.020
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
Hepatocellular carcinoma (HCC) is a common primary cancer associated with high incidences of genetic variations including chromosome instability. Moreover, it has been demonstrated that hepatitis C virus (HCV) is one of the major causes of HCC. However, no previous work has assessed whether HCV proteins are associated with the induction of chromosome instability. Here, we found that liver cell lines constitutively expressing full-length or truncated versions of the HCV genome show a high incidence of chromosome instability. In particular, the overexpression of HCV NS5A protein in cultured liver cells was found to promote chromosome instability and aneuploidy. Further experiments showed that NS5A-induced chromosome instability is associated with aberrant mitotic regulations, such as, an unscheduled delay in mitotic exit and other mitotic impairments (e.g. multi-polar spindles). Thus, our results indicate that HCV NS5A protein may be directly involved in the induction of chromosome instability via mitotic cell cycle dysregulation, and provide novel insights into the molecular mechanisms of HCV-associated hepatocarcinogenesis. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:22 / 34
页数:13
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