[Mechanism of hepatocarcinogenesis by hepatitis B virus]

Nihon Rinsho. 1993 Feb;51(2):364-9.
[Article in Japanese]

Abstract

The X gene product of hepatitis B virus (HBV) has a trans-activation function. The AP-1, AP-2, kappa B-like, and C/EBP-like sequences, and the 26-bp element in HBV enhancer were identified as X-responsive elements. Although the X protein possesses a transcriptional activation domain, it doesn't bind to the X-responsive elements. However, CREB/ATF-2 becomes able to bind to a CRE-related sequence in the 26-bp element once it complexes with X protein. In addition, X protein was shown to have amino acid sequences homologous to the essential domain of Kunitz-type serine protease inhibitors and directly interacted with the protease, tryptase TL2. Results suggest that X protein modulates the tryptase TL2 activity, which may be involved in the proteolytic cleavage of cellular transcription factors.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Amino Acid Sequence
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / microbiology*
  • Chymases
  • Genes, Viral
  • Hepatitis B virus / genetics*
  • Humans
  • Liver Neoplasms / genetics
  • Liver Neoplasms / microbiology*
  • Molecular Sequence Data
  • Sequence Homology, Amino Acid
  • Serine Endopeptidases / metabolism
  • Serine Proteinase Inhibitors
  • Transcriptional Activation
  • Tryptases
  • Viral Proteins

Substances

  • Serine Proteinase Inhibitors
  • Viral Proteins
  • Serine Endopeptidases
  • chymase 2
  • Chymases
  • Tryptases