Literature DB >> 16616934

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

Kwan-Hyuck Baek1, Hye-Young Park, Chang-Mo Kang, So-Jung Kim, Sook-Jung Jeong, Eun-Kyung Hong, Joong-Won Park, Young-Chul Sung, Tetsuro Suzuki, Chang-Min Kim, Chang-Woo Lee.   

Abstract

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.

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Year:  2006        PMID: 16616934     DOI: 10.1016/j.jmb.2006.03.020

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  13 in total

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9.  Micronuclei formation in liver fibrosis samples from patients infected by hepatitis C virus.

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10.  Hepatitis C virus NS5A protein down-regulates the expression of spindle gene Aspm through PKR-p38 signaling pathway.

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Journal:  J Biol Chem       Date:  2008-08-26       Impact factor: 5.157

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