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1989 Fiscal Year Final Research Report Summary

Production of hepatoma in cirrhotic liver and its prediction

Research Project

Project/Area Number 63480286
Research Category

Grant-in-Aid for General Scientific Research (B)

Allocation TypeSingle-year Grants
Research Field General surgery
Research InstitutionAkita University

Principal Investigator

KOYAMA Kenji  Akita Univ. School of Med. Dep. of Surg. Professor, 医学部, 教授 (80004638)

Co-Investigator(Kenkyū-buntansha) ASANUMA Yoshihiro  Ditto Lecturer, 医学部, 講師 (20142937)
Project Period (FY) 1988 – 1989
KeywordsCirrhosis / Hepatoma / DNA / Cell cycle / DEN / TAA / G-GTP
Research Abstract

I Animal experiments
1. Experimental production of hepatic cirrhosis in rat
Continuous oral administration of thioacetamide (TAA) was performed in rats, and liver cirrhosis was produced after 24 weeks.
1) DNA damage of cirrhotic hepatocytes was revealed by nick translation method, and becomes increasingly serious with the prolongation of TAA administration. The DNA damage was supposed to have some relationship with carcinogenic gene( c-myc ).
2) In the cirrhotic liver above-mentioned, DNA analysis by the flow cytometry and cll cycle by labeling index after BrdU administration. As the results, hepatocyte cell cycle increase at 3rd and 16th week after TAA administration, however, it decreases at 24th - 32nd week, when the liver cirrhosis was established. That is, the regeneration nodule shows no particular increase of cell cycle. As to bile duct epithelium, the peak of cell cycle appeared earlier than in hepatocyte. The labeling index at 24th was very high, when the so-called cholangio-fibrosis -- alleged as the precancerous state. From these results, liver cirrhosis in rat dose not develop into hepatoma.
3) Importance of initiator in production of hepatoma in cirrhosis was studied. As the cancer initiator, diethylnitrosamine( DEN ) was administrated only once and TAA was administered as mentioned above. The cell cyle increases in this model comparing with the rats treated with DEN alone and TAA alone. At the same time, there were many hepatocyte which revealed positive G GTP Cancer specific enzyme, in regenerating nodules.These results indicates that indicator, although only one time, is very important in carcinogenesis of hepatoma in cifrhosis

  • Research Products

    (8 results)

All Other

All Publications (8 results)

  • [Publications] 武正寿明・小山研二他: "チオアセトアミド投与を受けたラット肝細胞おけるDNA損傷生成とその修復の時間的差異" 医学のあゆみ. 146. 57-58 (1988)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 吉田節朗・小山研二他: "肝切除後の残存肝DNA損傷と肝再生" 日本外科学会雑誌. 90. 1814-1814 (1989)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 佐藤泰彦・小山研二他: "ラットにおけるチオアセトアシドによる肝硬変の細胞回転について" 肝臓(掲載予定). 31. (1990)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 武正寿明: "ニックトランスレ-ション法を用いて測定したラット肝細胞核内DNA損傷と修復合成との関係" 秋田医学. 16. 309-318 (1989)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takemasa, T., Koyama, K. et al.: "Time lag between DNA damage and DNA synthesis in the rat hepatocyte after administration of thioacetamide." "Igaku no Ayumi". 146:57-58, 1988.

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yoshida, S., Takemasa, T., Koyama, K. et al.: "DNA damage and hepatic regeneration after partial hepatectomy." "Japanese Journal of Surgery". 90:1814, 1989.

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Sato, Y., Koyama, K, et al.: "Cell kinetic studies on the experimental liver cirrhosis induced by thioacetamide in the rat." "Acta Hepatologica Japonica" accepted and in press.

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takemasa, T.: "Damage and repair of nuclear DNA of rat hepatocytes measured by nick translation and unscheduled DNA synthesis." "Akita Igaku". 16:309-318, 1989.

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 1993-03-26  

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