Genotypic variability of hepatitis viruses associated with chronic infection and the development of hepatocellular carcinoma

被引:32
作者
Pujol, FH [1 ]
Devesa, M [1 ]
机构
[1] Inst Venezolano Invest Cient, CMBC, Mol Virol Lab, Caracas 1020A, Venezuela
关键词
hepatitis; hepatocellular carcinoma; molecular epidemiology; genotype; cancer;
D O I
10.1097/01.mcg.0000170770.49394.92
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
At least five hepatitis viruses are known to date. Infection by enterically transmitted viruses (HAV and HEV) is generally benign compared with the disease caused by parenterally transmitted viruses (HBV, HCV, and HDV). Chronic infection by HBV is common and may evolve to cirrhosis and hepatocellular carcinoma (HCC). Eight HBV genotypes (A-H) have been described, with the South American genotype F being the most divergent. Seven clades of HDV have been described; among them, the South American genotype III is associated to a high frequency of fulminant hepatitis. HCV infection leads to a high rate of chronicity and HCC. From the six HCV genotypes, infection with genotype 1 might have the worst prognostic. Chronic infection by HCV and HBV is the major risk factor for HCC, which occurs, in the majority of the cases, as a consequence of cirrhosis. However, there is growing evidence that some HBV and HCV proteins might contribute to the generation of HCC. Some HBV and HCV variants and specific mutations within the viral genomes might be more frequently associated with the evolution to HCC. Although more studies are needed, emerging evidence indicates that it might be important to address the genetic variability of these viruses and their contribution to the development of HCC.
引用
收藏
页码:611 / 618
页数:8
相关论文
共 162 条
[1]
Aguilar MS, 2001, ANN TROP MED PARASIT, V95, P187, DOI 10.1080/00034980120042944
[2]
Phylogenetic origin of hepatitis B virus strains with precore C-1858 variant [J].
Alestig, E ;
Hannoun, C ;
Horal, P ;
Lindh, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (09) :3200-3203
[3]
Allain JP, 2000, VOX SANG, V78, P243
[4]
The prevalence of hepatitis C virus infection in the United States, 1988 through 1994 [J].
Alter, MJ ;
Kruszon-Moran, D ;
Nainan, OV ;
McQuillan, GM ;
Gao, FX ;
Moyer, LA ;
Kaslow, RA ;
Margolis, HS .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (08) :556-562
[5]
Genotype H: a new Amerindian genotype of hepatitis B virus revealed in Central America [J].
Arauz-Ruiz, P ;
Norder, H ;
Robertson, BH ;
Magnius, LO .
JOURNAL OF GENERAL VIROLOGY, 2002, 83 :2059-2073
[6]
Arbuthnot P, 2001, INT J EXP PATHOL, V82, P77, DOI 10.1111/j.1365-2613.2001.iep178.x
[7]
Molecular properties, biology, and clinical implications of TT virus, a recently identified widespread infectious agent of humans [J].
Bendinelli, M ;
Pistello, M ;
Maggi, F ;
Fornai, C ;
Freer, G ;
Vatteroni, ML .
CLINICAL MICROBIOLOGY REVIEWS, 2001, 14 (01) :98-+
[8]
Molecular mechanisms underlying the development of hepatocellular carcinoma [J].
Bergsland, EK .
SEMINARS IN ONCOLOGY, 2001, 28 (05) :521-531
[9]
Antigenic diversity of hepatitis B virus strains of genotype F in Amerindians and other population groups from Venezuela [J].
Blitz, L ;
Pujol, FH ;
Swenson, PD ;
Porto, L ;
Atencio, R ;
Araujo, M ;
Costa, L ;
Monsalve, DC ;
Torres, JR ;
Fields, HA ;
Lambert, S ;
Van Geyt, C ;
Norder, H ;
Magnius, LO ;
Echevarría, JM ;
Stuyver, L .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (03) :648-651
[10]
Calcium signaling by HBx protein in hepatitis B virus DNA replication [J].
Bouchard, MJ ;
Wang, LH ;
Schneider, RJ .
SCIENCE, 2001, 294 (5550) :2376-2378