The roles of hepatitis C virus proteins in modulation of cellular functions: A novel action mechanism of the HCV core protein on gene regulation by nuclear hormone receptors

被引:19
作者
Watashi, K [1 ]
Shimotohno, K [1 ]
机构
[1] Kyoto Univ, Inst Virus Res, Dept Viral Oncol, Sakyo Ku, Kyoto 6068507, Japan
关键词
D O I
10.1111/j.1349-7006.2003.tb01381.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatitis C virus (HCV) is one of the major causative agents inducing the development of hepatocellular carcinoma. The underlying mechanism of HCV pathogenesis, however, is largely unknown. Recent reports have implicated specific HCV proteins in persistent HCV infection, reduction of interferon sensitivity, and the modulation of cell proliferation, including alterations in apoptotic responses. However, the roles of these viral proteins remain controversial, because of conflicting results. Thus, it remains necessary to elucidate the precise molecular mechanisms through which the viral proteins influence cell growth and pathogenesis. In this review, after briefly describing what is known about the roles of the HCV proteins, in particular HCV core protein (core), in the modulation of cellular functions, we propose a novel molecular mechanism of the core in modulating gene expression via activation of nuclear hormone receptors.
引用
收藏
页码:937 / 943
页数:7
相关论文
共 42 条
[1]   Transforming growth factor betas and their receptors in human liver cirrhosis [J].
Baer, HU ;
Friess, H ;
Abou-Shady, M ;
Berberat, P ;
Zimmermann, A ;
Gold, LI ;
Korc, M ;
Büchler, MW .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1998, 10 (12) :1031-1039
[2]   Hepatitis C virus core protein shows a cytoplasmic localization and associates to cellular lipid storage droplets [J].
Barba, G ;
Harper, F ;
Harada, T ;
Kohara, M ;
Goulinet, S ;
Matsuura, Y ;
Eder, G ;
Schaff, Z ;
Chapman, MJ ;
Miyamura, T ;
Brechot, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (04) :1200-1205
[3]   Sp110 localizes to the PML-Sp100 nuclear body and may function as a nuclear hormone receptor transcriptional coactivator [J].
Bloch, DB ;
Nakajima, A ;
Gulick, T ;
Chiche, JD ;
Orth, D ;
de la Monte, SM ;
Bloch, KD .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (16) :6138-6146
[4]   Identification and characterization of a histone binding site of the non-structural protein 3 of hepatitis C virus [J].
Borowski, P ;
Kühl, R ;
Laufs, R ;
zur Wiesch, JS ;
Heiland, M .
JOURNAL OF CLINICAL VIROLOGY, 1999, 13 (1-2) :61-69
[5]  
CEMY A, 1999, HEPATOLOGY, V30, P595
[6]   Hepatitis C virus core from two different genotypes has an oncogenic potential but is not sufficient for transforming primary rat embryo fibroblasts in cooperation with the H-ras oncogene [J].
Chang, J ;
Yang, SH ;
Cho, YG ;
Hwang, SB ;
Hahn, YS ;
Sung, YC .
JOURNAL OF VIROLOGY, 1998, 72 (04) :3060-3065
[7]   Direct interaction of hepatitis C virus core protein with the cellular lymphotoxin-beta receptor modulates the signal pathway of the lymphotoxin-beta receptor [J].
Chen, CM ;
You, LR ;
Hwang, LH ;
Lee, YHW .
JOURNAL OF VIROLOGY, 1997, 71 (12) :9417-9426
[8]  
Dubuisson J, 1998, Bull Mem Acad R Med Belg, V153, P343
[9]   Alterations of RB1, p53 and Wnt pathways in hepatocellular carcinomas associated with hepatitis C, hepatitis B and alcoholic liver cirrhosis [J].
Edamoto, Y ;
Hara, A ;
Biernat, W ;
Terracciano, L ;
Cathomas, G ;
Riehle, HM ;
Matsuda, M ;
Fujii, H ;
Scoazec, JY ;
Ohgaki, H .
INTERNATIONAL JOURNAL OF CANCER, 2003, 106 (03) :334-341
[10]   Expression of hepatitis C virus proteins induces distinct membrane alterations including a candidate viral replication complex [J].
Egger, D ;
Wölk, B ;
Gosert, R ;
Bianchi, L ;
Blum, HE ;
Moradpour, D ;
Bienz, K .
JOURNAL OF VIROLOGY, 2002, 76 (12) :5974-5984