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Hepatitis C virus core protein promotes proliferation of human hepatoma cells through enhancement of transforming growth factor α expression via activation of nuclear factor-κB
  1. Y Sato,
  2. J Kato,
  3. R Takimoto,
  4. K Takada,
  5. Y Kawano,
  6. K Miyanishi,
  7. M Kobune,
  8. Y Sato,
  9. T Takayama,
  10. T Matunaga,
  11. Y Niitsu
  1. Fourth Department of Internal Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan
  1. Correspondence to:
    J Kato
    Fourth Department of Internal Medicine, Sapporo Medical University School of Medicine, South-1, West-16, Chuo-ku, Sapporo 060-8543,Japan; jkato{at}sapmed.ac.jp

Abstract

Background: Hepatitis C virus (HCV) infection is a major cause of human hepatocellular carcinoma (HCC). The precise mechanism of hepatocarcinogenesis in humans by HCV is currently unclear. It was recently shown, however, that transgenic mice with the HCV core gene often develop HCC, suggesting tumorigenic activity of the HCV core protein. Further, the HCV core protein expressed in HepG2 cells transfected with the core gene was shown to stimulate proliferation of transfectants through activation of nuclear factor-κB (NF-κB). The downstream target molecule(s) of NF-κB activated by the HCV core protein to evoke cell proliferation is not yet identified. Transforming growth factor (TGF) α, which is often overexpressed in various tumour tissues such as HCC, has been shown to stimulate hepatocyte proliferation through activation of the mitogen-activated protein kinase or extracellular signal-related protein kinase (MAPK/ERK) cascade.

Aims: To explore the possibility that TGFα might be a target molecule for NF-κB activated by the HCV core, and that TGFα participates in the growth promotion of the core transfectants in an autocrine manner, activating the MAPK/ERK pathway.

Methods: A HCV core expression vector was transfected into human hepatoma Huh-7, HepG2 and Hep3B cells. NF-κB activity was examined by an electrophoretic mobility shift assay. TGFα transcription was assessed by a luciferase reporter assay. TGFα protein was determined by immunoblot and ELISA. MAPK/ERK activity was examined by an in vitro kinase assay. Cell proliferation was assessed by a water-soluble tetrazolium salt-1 assay.

Results: In the HCV core transfectants, NF-κB bound to the κB site in the TGFα proximal promoter region, resulting in an increase in TGFα transcription. Immunoblot as well as ELISA showed increased TGFα expression in the HCV core transfectants. SN50, a specific inhibitory peptide for NF-κB, cancelled HCV core-induced TGFα expression. HCV core protein increased cell proliferation as well as ERK activity of the HCV core transfectants as compared with the mock transfectants. The growth-promoting activity and activation of ERK by the HCV core protein were negated by treatment with anti-TGFα antibodies.

Conclusions: These results suggest that the HCV core protein promotes proliferation of human hepatoma cells by activation of the MAPK/ERK pathway through up regulation of TGFα transcription via activation of NF-κB. Our finding provides a new insight into the mechanism of hepatocarcinogenesis by HCV infection.

  • EGF, epidermal growth factor
  • ERK, extracellular signal-regulated kinase
  • FBS, fetal bovine serum
  • HCC, hepatocellular carcinoma
  • HCV, hepatitis C virus
  • MAPK, mitogen-activated protein kinase
  • MEK, MAPK kinase
  • NF-κB, nuclear factor-κB
  • PBS, phosphate-buffered saline
  • PCR, polymerase chain reaction
  • SDS-PAGE, sodium dodecyl sulphate-polyacrylamide gel electrophoresis
  • TGFα, transforming growth factor α
  • TNF, tumour necrosis factor

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Footnotes

  • Published Online First 31 March 2006

  • Funding: Supported in part by a grant-in-aid for scientific research (14570487 to JK) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.

  • Competing interests: None declared.

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