Regulatory mechanisms of viral hepatitis B and C

被引:71
作者
Waris, G [1 ]
Siddiqui, A [1 ]
机构
[1] Univ Colorado, Hlth Sci Ctr, Program Mol Biol, Dept Microbiol, Denver, CO 80262 USA
关键词
ER stress; hepatitis B virus; hepatitis C virus; NF-kappa B; oxidative stress; STAT-3;
D O I
10.1007/BF02970150
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Of all the hepatitis viruses, only the hepatitis B virus (HBV) and hepatitis C virus (HCV) cause chronic hepatitis, which can progress to cirrhosis and hepatocellular carcinoma. In this review, we discuss how these two biologically diverse viruses use common pathways to induce oxidative stress and activation of key transcription factors, known to be involved in inflammatory processes in cells. Activation of NF-kappaB and STAT-3 most likely contribute to the progression of viral infections to chronic hepatitis and liver oncogenesis associated with HBV and HCV infections. In this review, we focus on the mechanisms of action of HBx and HCV NS5A proteins in inducing intracellular events associated with the viral infections.
引用
收藏
页码:311 / 321
页数:11
相关论文
共 99 条
  • [31] Mitochondria and apoptosis
    Green, DR
    Reed, JC
    [J]. SCIENCE, 1998, 281 (5381) : 1309 - 1312
  • [32] Hepatitis B virus pX targets TFIIB in transcription coactivation
    Haviv, I
    Shamay, M
    Doitsh, G
    Shaul, Y
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (03) : 1562 - 1569
  • [33] Association between chronic hepatitis C infection and hepatocellular carcinoma in a Scottish population
    Haydon, GH
    Jarvis, LM
    Simmonds, P
    Harrison, DJ
    Garden, OJ
    Hayes, PC
    [J]. GUT, 1997, 40 (01) : 128 - 132
  • [34] Mammalian transcription factor ATF6 is synthesized as a transmembrane protein and activated by proteolysis in response to endoplasmic reticulum stress
    Haze, K
    Yoshida, H
    Yanagi, H
    Yura, T
    Mori, K
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (11) : 3787 - 3799
  • [35] Intracellular localization of the hepatitis B virus HBx protein
    Henkler, F
    Hoare, J
    Waseem, N
    Goldin, RD
    McGarvey, MJ
    Koshy, R
    King, IA
    [J]. JOURNAL OF GENERAL VIROLOGY, 2001, 82 : 871 - 882
  • [36] PROTEOLYTIC PROCESSING AND MEMBRANE ASSOCIATION OF PUTATIVE NONSTRUCTURAL PROTEINS OF HEPATITIS-C VIRUS
    HIJIKATA, M
    MIZUSHIMA, H
    TANJI, Y
    KOMODA, Y
    HIROWATARI, Y
    AKAGI, T
    KATO, N
    KIMURA, K
    SHIMOTOHNO, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) : 10773 - 10777
  • [37] Hepatitis C: The clinical spectrum of disease
    Hoofnagle, JH
    [J]. HEPATOLOGY, 1997, 26 (03) : S15 - S20
  • [38] Proteasome complex as a potential cellular target of hepatitis B virus X protein
    Huang, JK
    Kwong, J
    Sun, ECY
    Liang, TJ
    [J]. JOURNAL OF VIROLOGY, 1996, 70 (08) : 5582 - 5591
  • [39] Characterization of the mitochondrial association of hepatitis B virus X protein, HBx
    Huh, KW
    Siddiqui, A
    [J]. MITOCHONDRION, 2002, 1 (04) : 349 - 359
  • [40] Selectable subgenomic and genome-length dicistronic RNAs derived from an infectious molecular clone of the HCV-N strain of hepatitis C virus replicate efficiently in cultured Huh7 cells
    Ikeda, M
    Yi, MK
    Li, K
    Lemon, SA
    [J]. JOURNAL OF VIROLOGY, 2002, 76 (06) : 2997 - 3006