HBX-Mediated Migration of HBV-Replicating HepG2 Cells: Insights on Development of Hepatocellular Carcinoma

被引:11
作者
Feng, Huixing [1 ]
Zhang, Jianhua [1 ]
Li, Xi [1 ]
Chen, Wei Ning [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
来源
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY | 2009年
关键词
HEPATITIS-B-VIRUS; RHO-GTPASES; ADHESION; INFECTION; BIOLOGY; INVOLVEMENT; EXPRESSION; KINASE; FAMILY; MATRIX;
D O I
10.1155/2009/930268
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Hepatitus B virus (HBV) is a major cause of the development of hepatpcellular carcinoma (HCC). One of the significant characteristics of tumor progression is cell migration which is reflective of cytoskeletal dynamics. The Rho GTPases contribute to a multiple cellular processes, including the cellular cytoskeletal reorganization and motility. It has been found that some Rho GTPases have oncogenic activity and can promote cancer cell invasion. Here we discuss one of the Rho GTPases, Rac1 can be activated by HBV replication and such activation results in the high motility of HBV-replicating cells. The enhanced cell motility can be interestingly alleviated by the mutation at the sites of proline rich domain located in HBX. Our findings may provide new insights on the mechanism of HCC development associated with chronic HBV infection. Copyright (C) 2009 Huixing Feng et al.
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页数:6
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