• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Study on Epithelial-Mesenchymal Interaction During Promotion Stage of Carcinogenesis

Research Project

Project/Area Number 01570205
Research Category

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

Allocation TypeSingle-year Grants
Research Field Experimental pathology
Research InstitutionSapporo Medical Collge

Principal Investigator

ENOMOTO Katsuhiko  Sapporo Medical Collge, Dept. of Pathology, Associate Professor, 医学部(病理学), 助教授 (20151988)

Co-Investigator(Kenkyū-buntansha) HATTORI Atsuo  Sapporo Medical Collge, Dept. of Pathology, Instructor, 医学部(病理学), 助手 (90208538)
MORI Michio  Sapporo Medical Collge, Dept. of Pathology, Professor, 医学部(病理学), 教授 (00045288)
池田 健  札幌医科大学, 医学部, 助手 (40202890)
Project Period (FY) 1989 – 1990
Project Status Completed (Fiscal Year 1990)
Budget Amount *help
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1990: ¥200,000 (Direct Cost: ¥200,000)
Fiscal Year 1989: ¥1,700,000 (Direct Cost: ¥1,700,000)
KeywordsEpithelial-mesenchymal interaction / Carcinogenesis / Co-culture / Gap junction / Tight junction / 発癌プロモ-ション過程 / 細胞接着装置 / ギャップ結合 / コネクシン32 / 肝芽腫細胞 / 分化誘導 / 乳癌細胞 / 造腫瘍性 / 初代培養肝細胞 / 培養肝癌細胞 / 血管内皮細胞 / 上皮・間葉相互作用 / 分化
Research Abstract

1. Analysis of epithelial-mesenchymal interaction by the co-culture system.
Although the cultured hepatocytes rapidly lost their epithelial morphology, rat hepatocytes co-cultured with bovine aortic endothelial cells maintained their epithelial morphology and trabecular arrangement more than 2 weeks. Rapid appearance of bilecanaliculus like structures and reappearance of intercellular communication ability which was assayed by microinjection of fluorescent dye were also observed in the co-cultured hepatocytes. These suggest that the contact with endothelial cells is important for maintaining the differentiated phenotypes of the cultured hepatocytes.
Co-culture experiments were also carried out using hepatoma cell line HuH7 and hepatoblastoma cell line HuH6, HuH7 did not show any phenotypes of differentiation by the co-culture with endothelial cells, whereas proliferation of endothelial cells was induced. Thus, it is suggested that HuH7 may produce endothelial cell growth factors. On the … More other hand, HuH6 co-cultured with BALB3T3 cells showed reorganization of cell junction structures and reappearance of intercellular communication ability, suggesting the induction of differentiated phenotypes in HuH6 by the co-culture with fibroblasts.
2. Changes of the cell junction molecules during promotion stage of hepatocarcinogenesis.
In order to study alterations of cell junction molecules during rat hepatocarcinogenesis, antibodies against gap junction protein connexin 32 and tight junction protein were generated. Specificity of these antibodies was determined by immunoelectronmicroscopic examination and Western blot analysis. Preneoplastic and neoplastic rat liver lesions induced by an intraperitoneal injection of diethylnitrosamine were examined using these antibodies. The results indicated a great decrease of connexin 32 and tight junction proteins in the hyperplastic nodules and liver cancers. Thus, it is suggested t hat changes of cell junction molecules, which consist of the cell-cell recognition system, occur during promotion stage of hepatocarcinogenesis. Less

Report

(3 results)
  • 1990 Annual Research Report   Final Research Report Summary
  • 1989 Annual Research Report
  • Research Products

    (26 results)

All Other

All Publications (26 results)

  • [Publications] 榎本 克彦,中島 康雄 他: "発癌と局所因子" Medical Immunology. 19. 339-343 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] 榎本 克彦,鐘 雲: "肝細胞の癌化と細胞膜の異常ー接着装置特にgap junctionを中心としてー" 肝胆膵. 21. 773-779 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Sawaki,M.,Enomoto,K.,et al.: "Phenotype of preneoplastic and neoplastic liver lesions during spontaneous liver carcinogenesis of LEC rats" Carcinogenesis. 11. 1857-1861 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Nakajima,Y.,Enomoto,K.,et al.: "Immuno electron microscopic and immunohis to chemical demonstration of the connexin32 gap janction protein in rat liver." J.Clin.Electron microscopy. 23. 140-141 (1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Enomoto,K.,Takahashi,H.Mori,M.: "A new rat model for the study of hepatocarcinogenesis" J.Gastroenterol.Hepatol. (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] 佐藤 睦,榎本 克彦: "ヒト肝芽腫細胞の分化形項誘導に関する研究ー分化誘導物質ならびに線維芽細胞とのco‐cultureによる影響ー" 札幌医学雑誌. 60. (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Yamasaki,H.,Enomoto,K.,et al: "IARC Scientific Publication no,92 “Cell differentiation,Genes and Cancer"" Oxford University Press, 203 (1988)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Enomoto, K., et al.: "Carcinogenesis and tissue factors." Medical Immunology. 19. 339-343 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Enomoto, K., et al.: "Liver carcinogenesis and changes of cell membrane. -changes of cell junctions-" Kan-Tan-Sui. 21. 773-779 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Sawaki, M., Enomoto, K., et al.: "Phenotype of preneoplastic and neoplastic liver lesions during spontaneous liver carcinogenesis of LEC rats." Carcinogenesis. 11. 1857-1861 (1990)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Nakajima, Y., Enomoto, K., et al.: "Immunoelectronmicroscopic and immunohistochemical demonstration of the connexin 32 gap junction protein in rat liver." J. Clin. Electronmicroscopy. (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Enomoto, K., et al.: "A new rats model for the study of hepatocarcinogenesis." J. Gastroenterol. Hepatol.(1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Satoh, I. M., and Enomoto, K.: "Study of differentiation in human hepatoblastoma cells : changes in cell properties by differentiation-inducing agents and co-culture with fibroblastic cells." Sapporo Med. J.60. (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] Yamasaki, H., Enomoto, K., et al.: ""Cell differentiation, Genes and Cancer. "" IARC Scientific Publication No. 92. Oxford University Press. 57-74 (1988)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1990 Final Research Report Summary
  • [Publications] 榎本 克彦,中島 康雄,他: "発癌と局所因子" Medical Immunology. 19. 339-343 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] 榎本 克彦,鐘雲,他: "肝細胞の癌化と細胞膜の異常 ー接着装置特にgap junctionを中心としてー" 肝胆膵. 21. 773-779 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] Sawaki,M.,Enomoto,K.,et al.: "Phenotype of preneoplastic and neoplstic liver lesions during spontaneous liver carcinogenesis of LEC rats." Carcinogensis. 11. 1857-1861 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] Enomoto,K.,Takahashi,H.,Mori,M.: "A new rat model for the study of hepatocarcinogenesis." J.Gastroenterol.Hepatol.(1991)

    • Related Report
      1990 Annual Research Report
  • [Publications] Nakajima,Y.,Enomoto,K.,et al.: "Immunoelectron microscopic and immunohisto chemical demonstration of the connexin 32 gap junction protein in rat liver." J.Clin.Electronmicroscopy. (1991)

    • Related Report
      1990 Annual Research Report
  • [Publications] 佐藤 睦,榎本 克彦: "ヒト肝芽腫細胞の分化形質誘導に関する研究 ー分化誘導物質ならびに線椎芽細胞とのcoーculture" 札幌医学雑誌. (1991)

    • Related Report
      1990 Annual Research Report
  • [Publications] Yamasaki,H.,Enomoto,K.,Fitzgerald,D.J.et al: "Role of intercellular communication in the control of critical gene expression during multistage carcinogenesis" IARC Scientific Publication,No.92. 57-75 (1988)

    • Related Report
      1989 Annual Research Report
  • [Publications] Ikeda,T.,Sawada,N.,Fujinaga,K.et al: "c-H-ras gene is expressed at the G_1 phase in primary cultures of hepatocytes." Exp.Cell.Res.185. 292-296 (1989)

    • Related Report
      1989 Annual Research Report
  • [Publications] Takahashi,H.,Enomoto,K.,Nakajima,Y.and Mori,M: "High sensitivity of the LEC rat liver to the carcinogenic effect of diethyl nitrosamine." Cancer Letters,in press.

    • Related Report
      1989 Annual Research Report
  • [Publications] Sawaki,M.,Enomoto,K.,Takahashi,H.et al: "Phenotypic changes of preneoplastic and neoplastic lesions during sponteneous liver carcinogenesis of LEC rat." Manuscript,in preparation.

    • Related Report
      1989 Annual Research Report
  • [Publications] 榎本克彦,他: "発癌と局所因子" Medical Immunology,.

    • Related Report
      1989 Annual Research Report
  • [Publications] 榎本克彦,他: "細胞のがん化" からだの科学.

    • Related Report
      1989 Annual Research Report

URL: 

Published: 1989-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi