Temporal treatment with interferon-beta prevents hepatocellular carcinoma in hepatitis B virus X gene transgenic mice

J Hepatol. 2008 Feb;48(2):255-65. doi: 10.1016/j.jhep.2007.09.012. Epub 2007 Nov 20.

Abstract

Background/aims: The preventive effect of interferon (IFN) against hepatocellular carcinoma (HCC) has been confirmed clinically. We sought to determine whether the temporal administration of IFN-beta prevents hepatocarcinogenesis in a mouse model where HCC develops without necroinflammation.

Methods: Hepatocarcinogenic mice that are transgenic for the hepatitis B virus X gene (HBx-Tg) were treated with IFN-beta or saline (control) for three months, from 3 to 6 months of age, and the incidence of HCC was determined at 18 months of age. The effects of IFN-beta on DNA synthesis and apoptosis were tested.

Results: The incidence of HCC was significantly lower in the IFN-beta-treated mice than the controls (0 vs. 50%, P<0.01). Inhibition of DNA synthesis in hepatocytes by IFN-beta was observed in the livers of HBx-Tg, without any significant induction of apoptosis. Although the treatment of IFN-beta was temporal, the number of hepatocytes with DNA synthesis remained lower 3 and 12 months later in life.

Conclusions: Temporal administration of IFN-beta has a significant preventive effect on the occurrence of HCC in a mouse model where HCC develops without inflammation. The mechanisms are the inhibition of DNA synthesis and cell cycle progression of hepatocytes.

MeSH terms

  • Animals
  • Cells, Cultured
  • DNA / biosynthesis
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Humans
  • Interferon-beta / pharmacology
  • Interferon-beta / therapeutic use*
  • Liver Neoplasms, Experimental / pathology
  • Liver Neoplasms, Experimental / prevention & control*
  • Mice
  • Mice, Transgenic
  • S Phase / drug effects
  • STAT1 Transcription Factor / physiology
  • Signal Transduction
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Viral Regulatory and Accessory Proteins

Substances

  • STAT1 Transcription Factor
  • Trans-Activators
  • Viral Regulatory and Accessory Proteins
  • hepatitis B virus X protein
  • Interferon-beta
  • DNA