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Analysis of gene expression on interstitial cells of Cajal

Research Project

Project/Area Number 24590494
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Experimental pathology
Research InstitutionHyogo Medical University

Principal Investigator

ISOZAKI Koji  兵庫医科大学, 医学部, 非常勤講師 (00425117)

Co-Investigator(Kenkyū-buntansha) HIROTA Seiichi  兵庫医科大学, 医学部, 教授 (50218856)
Project Period (FY) 2012-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywordsカハールの介在細胞 / c-kit / GISTs / CADM1 / c-kit遺伝子 / c-kit 遺伝子
Outline of Final Research Achievements

By using cDNA library of interstitial cells of Cajal(ICCs), we first clarified that CADM1, one of cell adhesion molecules, is specifically expressed by ICCs. We investigated CADM1 expression in gastrointestinal stromal tumors (GISTs) which are considered to be originated from ICCs, and found that most of GISTs in the small intestine express CADM1, but most of gastric GISTs do not. The specific expression of CADM1 in small intestinal GISTs might mean that specific expression of CADM1 in ICCs in the small intestine. ICCs in different sites may show different protein expression pattern and may have different role.

Report

(4 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • 2012 Research-status Report
  • Research Products

    (4 results)

All 2015 2014 2013 2012

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (1 results)

  • [Journal Article] Gastrointestinal stromal tumors with exon8 c-kit gene mutation might occur at extragastric sites and have metastasis-prone nature2014

    • Author(s)
      Ito T,Yamamura M,Hirai T,Ishikawa T,Kanda T,Nakai T,Ohkouchi M,Hashikura Y,Isozaki K,Hirota S
    • Journal Title

      In J Clin Exp Pathology

      Volume: 7 Pages: 80248031-80248031

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Extracellular domain c-kit mutation with duplication of Ser501Ala502 found in gastrointestinal stromal tumors is more imatinib- and nilotinib-sensitive than that with duplication of Ala502Tyr5032013

    • Author(s)
      Liu N-N, Ohkouchi M, Hashikura Y, Kajimoto N, Matsuda I, Isozaki K, Toh Y, Takahashi T, Nishida T, Hirota S
    • Journal Title

      Lab Invest

      Volume: 93 Issue: 5 Pages: 502-507

    • DOI

      10.1038/labinvest.2013.43

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Characterization of novel germline c-kit gene mutation, KIT-Tyr553Cys, observed in a family with multiple gastrointestinal stromal tumors2012

    • Author(s)
      Nakai M, Hashikura Y, Ohkouchi M, Yamamura M, Akiyama T, Shiba K, Kajimoto N, Tsukamoto Y, Hao H, Isozaki K, Hirai T, Hirota S
    • Journal Title

      Lab Invest

      Volume: 92 Issue: 3 Pages: 451-457

    • DOI

      10.1038/labinvest.2011.165

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Presentation] c-kit遺伝子のexon8に変異を持つ消化管間葉系腫瘍にはimatinibによる分子標的治療が有効2015

    • Author(s)
      礒崎耕次
    • Organizer
      第16回関西がんチーム医療研究会
    • Place of Presentation
      大阪
    • Year and Date
      2015-02-28
    • Related Report
      2014 Annual Research Report

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Published: 2013-05-31   Modified: 2019-07-29  

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