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The expression of Angiopoietin and Tie receptor in colorectal cancer and its roles in proliferation and invasion

Research Project

Project/Area Number 17590351
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Experimental pathology
Research InstitutionNagasaki University

Principal Investigator

NAKAYAMA Toshiyuki  Nagasaki University, Graduate School of Biomedical Sciences, Atomic Bomb Disease Institute, Tumor and Diagnostic Pathology, Associate Professor, 大学院医歯薬学総合研究科, 准教授 (30284673)

Co-Investigator(Kenkyū-buntansha) SEKINE Ichiro  Nagasaki University, Professor and Chair, 大学院医歯薬学総合研究科, 教授 (60039922)
温 春陽  長崎大学, 大学院・医歯薬学総合研究科, 助手 (80346957)
Project Period (FY) 2005 – 2006
Project Status Completed (Fiscal Year 2006)
Budget Amount *help
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2006: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2005: ¥2,400,000 (Direct Cost: ¥2,400,000)
KeywordsColorectal cancer / Angiopoietin / Tie / Invasion / Differentiation
Research Abstract

There is strong evidence that tyrosine kinases are involved in the regulation of tumor progression, cellular growth and differentiation. Recently, many types of tyrosine kinase receptors have been reported, among which Tie-1 and 2 constitute a major class. Angiopoietin (Ang)-1 is known to be a ligand of the Tie-2 tyrosine kinase receptor. The objective of this study was to establish a comprehensive Tie-1 and 2 and Ang-1, 2 and 4 expression profile in colorectal adenocarcinoma cells.
To elucidate the involvement of Tie-1 and 2 and Ang-1, 2 and 4 in human colorectal adenocarcinomas, we examined 96 cases of surgically resected human colorectal adenocarcinoma by immunohistochemistry and molecular techniques.
Among the 96 cases of adenocarcinoma, 87 (90.6%), 92 (95.8%), 83 (86.5%), 89 (92.7%), and 76 cases (79.2%) showed positive staining in the cytoplasm of the carcinoma cells for the Tie-1 and 2, and Ang-1, 2 and 4 proteins, respectively. Histologically, the expression of Ties and Angs was variable. Tie and Ang expression patterns were correlated with several clinicopathological factors, but did not correlate with the presence of lymph node metastasis. Ang-1 and 2 proteins upregulated the tumor cell growth and the invasive activity. And it showed the deformation of tumor cell with the treatment of Ang-1 and 2. Ang-1 and 2 showed upregulated the MAPKinase and PI3Kinase pathways in tumor cells by western blot analyses. However, experiment is still going on.
Ties and Angs are highly expressed in human colorectal adenocarcinoma cells and correlated with histological differentiation, tumor progression in colorectal cancer. And the cell signaling pathway was upregulated by the treatment of Ang-1 and 2. These findings suggest that the Tie-Ang receptor-ligand complex is involved in the cellular differentiation and progression of human colorectal adenocarcinoma.

Report

(3 results)
  • 2006 Annual Research Report   Final Research Report Summary
  • 2005 Annual Research Report

Research Products

(2 results)

All 2007

All Journal Article (2 results)

  • [Journal Article] Expression of Angiopoietin-1, 2 and 4 and Tie-1 and 2 in gastrointestinal stromal tumor, leiomyoma and schwannoma.2007

    • Author(s)
      中山敏幸
    • Journal Title

      World Journal of Gastroenterology (印刷中)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Expression of Angiopoietin-1, 2 and 4 and Tie-1 and 2 in gastrointestinal stromal tumor, leiomyoma and schwannoma2007

    • Author(s)
      Toshiyuki Nakayama
    • Journal Title

      World Journal of Gastroenterology (Now printing)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2006 Final Research Report Summary

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Published: 2005-03-31   Modified: 2016-04-21  

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