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Function of Hepatitis B virus X gene in carcinogenesis of liven cells

Research Project

Project/Area Number 09670539
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Gastroenterology
Research InstitutionMie University

Principal Investigator

TAKASE koujiro  Mie University, Faculty of Medicine, Associate Professor, 医学部, 助教授 (00163204)

Co-Investigator(Kenkyū-buntansha) ITO Masaaki  Mie University, Hospital, Lecturer, 医学部・附属病院, 講師 (00223181)
SHIMIZU Atsuya  Mie University, Faculty of Medicine, Assistant, 医学部, 助手 (10283524)
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 1998: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1997: ¥2,500,000 (Direct Cost: ¥2,500,000)
KeywordsHBx / LBP / Two Hybrid System / Apoptosis / HBx / two hybrid / Ywo hybrid
Research Abstract

The X gene lesion of HBV from nine patients with hepatocellular carcinoma were amplified by PCR and sequenced. The X gene sequences were well conserved and no point mutations were detected compared to these form the healthy HBV carriers.
The laminin binding protein (LBP) was indentified as a protein interacting with X protein in the yeast two hybrid system. The interaction was confirmed by far western blot using recombinant GST- fusion proteins. As LBP was reported to have function in metastasis and proliferation of cancer cells via laminin receptor, we will continue to investigate the functions of these interaction in carcinogenesis of liver cells.
A specific antibody which could recognize X protein was developed and purified. The specificity of this antibody was confirmed by the evidence that this antibody could detect a single band of X protein expressed in both E. Coil (DH5α,45 kDa GST-fusion protein) and cultured cells (using pcDNA vector).
The X protein expressed in cultured cells transfected by pcDNA3.1(-)/Myc-His vector was stained mainly in the cytoplasm with granular pattern using both anti-X and anti-Myc antibodies. The expressed X protein was also observed in nucleus.
The X protein positive cells were diffusely observed in the liver tissues (biopsy form the patients with chronic active hepatitis B) and clustering positive cells were seen more frequently around the portal area.

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] Murata K.et al.: "Splenectomy enhances liver regeneration through tumor necrosis factor(TNF)-alpha following dimethy Initrosamine-induced cirrhchc rat model"Hepato・Gastroenterology. (in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Kazushi Sugimoto et al.: "Expression of functional CD40 in human hepatocellular carcinoma"Hepatology. (in press).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Murata K, Shiraki K, Takashe k, Furusaka A, Tameda Y: "splenectomy enhances liver regeneration through tumor necrosis factor (TNF)-alpha following dimethylnitrosamine-induced cirrhotic rat model"Hepato-Gastroenterology. in press.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Kazushi Sugimoto, Katsuya Shiraki, Takeshi Ito, katsuhiko Fujikawa, Koujiro takase, Yukihiko Tameda, Masami Moriyama, Takeshi Nakano: Hepatology. in press.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary

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Published: 1997-04-01   Modified: 2016-04-21  

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