Modulation of programmed cell death pathways by the hepatitis C virus

被引:12
|
作者
Aweya, Jude Juventus [1 ,2 ]
Tan, Yee-Joo [1 ,2 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Microbiol, Singapore 117597, Singapore
[2] ASTAR, Collaborat Antiviral Res Grp, Inst Mol & Cell Biol, Singapore, Singapore
来源
关键词
Hepatitis C virus; HCV; Infection; Replication; Programmed Cell Death; Apoptosis; Autophagy; Structural Proteins; Non-Structural Proteins; Prosurvival; Proapoptotic; Review; HCV CORE PROTEIN; ALPHA-MEDIATED APOPTOSIS; NONSTRUCTURAL 5A PROTEIN; INHIBITS APOPTOSIS; TRIGGERS APOPTOSIS; ENVELOPE PROTEINS; INDUCE APOPTOSIS; ION-CHANNEL; NS3; PROTEIN; P7;
D O I
10.2741/3709
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
Hepatitis C virus (HCV), a positive stranded RNA virus of the family Flaviviridae, is the major cause of non-A, non-B hepatitis worldwide. The HCV genome encodes a precursor polyprotein of similar to 3,000 amino acids that is processed co-translationally and post-translationally to give rise to viral structural and non-structural proteins. Nearly all of these viral proteins have been shown to modulate cell death via various mechanisms. In addition, studies using the replicon and recombinant HCV cell culture systems have yield important insights into the modulation of programmed cell death by HCV replication. Here, we summarize current knowledge on the modulation of apoptosis and other programmed cell death pathways by the HCV in these cell culture systems.
引用
收藏
页码:608 / 618
页数:11
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