Semin Liver Dis 1999; 19(3): 253-262
DOI: 10.1055/s-2007-1007115
ORIGINAL ARTICLE

© 1999 by Thieme Medical Publishers, Inc.

Hepatitis B Virus Infection and Hepatocellular Carcinoma: Molecular Genetics and Clinical Perspectives

Pei-Jer Chen, Ding-Shinn Chen
  • Hepatitis Research Center, Department of Internal Medicine, National Taiwan University Hospital and Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University
Further Information

Publication History

Publication Date:
17 March 2008 (online)

ABSTRACT

Chronic hepatitis B progresses across a spectrum of asymtomatic carriers, active hepatitis, and liver cirrhosis. With more advanced disease stage, the risk for developing hepatocellular carcinoma (HCC) becomes higher. Recent studies suggest that this progressive risk may reflect an accumulation of multistage genetic mutations in the chromosomes of affected hepatocytes. Mutations of the known candidate genes such as p53 and β-catenin have been found. Recent genome-wide analysis of HCC chromosomes by comparative genomic hybridization or loss of heterozygosity have identified more new loci implicated in hepatocarcinogenesis. Persistent hepatitis B is essential for inducing these mutations through immune-mediated injuries of the hepatocytes and the resulting hyperplasia. Prevention of hepatitis B by active immunization effectively interrupts persistent viral infections in children and sub-sequently reduces the risk of childhood HCC. Treatment for chronic hepatitis B by interferon or antiviral analogues can control hepatitis B activity, but its effect on controlling HCC remains to be seen. Insights for the hepatocarcino-genesis process should come from a multidisciplinary collaboration to explore important viral and host genes so that new approaches to diagnosis and treatment can be developed.

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