Association between hepatitis B virus core promoter rearrangements and hepatocellular carcinoma

被引:21
作者
Laskus, T [1 ]
Radkowski, M
Nowicki, M
Wang, LF
Vargas, H
Rakela, J
机构
[1] Univ Pittsburgh, Thomas E Starzl Transplantat Inst, Pittsburgh, PA 15260 USA
[2] Univ So Calif, Sch Med, Los Angeles, CA USA
[3] Univ Pittsburgh, Med Ctr, Div Gastroenterol & Hepatol, Pittsburgh, PA USA
关键词
D O I
10.1006/bbrc.1998.8249
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Hepatitis B virus (HBV) is the major etiological agent of hepatocellular carcinoma (HCC). Whether any particular viral variants are associated with HCC is unknown. We studied 53 Gambian patients with HCC and 33 HBsAg positive controls. A functional part of HBV core promoter and whole precore region were sequenced directly and/or after cloning. HBV DNA was amplified from sera from 27 HCC patients and in all controls. Fourteen (52%) patients and 12 (36%) controls (NS) were found to harbor an HBV strain with G to A transition mutation at position 1896 leading to HBeAg negative phenotype. Nine (33%) HCC patients and 2 (6%) controls (p<0.01) harbored a mixture of wild type and HBV strains with deletions/insertions; strong consensus sequences for topoisomerase I breakage were located in the vicinity of these changes. In Africa, HCC is associated with HBV strains that have deletions/insertions in the HBV core promoter region. (C) 1998 Academic Press.
引用
收藏
页码:812 / 814
页数:3
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