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Analysis of the cell growth mechanism by ZIC2 transcription factor in pancreatic cancer cells.

Research Project

Project/Area Number 23790424
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Human pathology
Research InstitutionAichi Medical University

Principal Investigator

INAGUMA Shingo  愛知医科大学, 医学部, 講師 (80410786)

Project Period (FY) 2011 – 2013
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywordsヘッジホッグ / 膵臓癌 / ZIC2 / アポトーシス / 細胞増殖 / 転写因子
Research Abstract

ZIC2 is one of five members of ZIC family gene those are indispensable for the development of central nervous system. Recently, we uncovered that ZIC2 is a unique member which is expressed in all (11/11) of the pancreatic ductal adenocarcinoma (PDAC) cell lines we tested.
From the cDNA expression microarray analysis, we identified ANXA8 and FGFR3 as ZIC2 transcriptional targets. Furthermore, we uncovered that forced expression of ANXA8 reduced the apoptotic cell death of the ZIC2-knockdown PDAC cells and that ZIC2 accelerated ERK phosphorylation in FGFR3 dependent manner. Although ZIC2, ANXA8 and FGFR3 expressions were immunohistochemically under-detectable levels in the normal pancreatic duct, their expression was prominent in PanIN and PDAC cells.
Our in vitro and in vivo experimental results indicate that ZIC2-ANXA8 and ZIC2-FGFR3-ERK axis are important signaling pathways for the regulation of apoptosis and cell proliferation in the PDAC development.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • 2011 Research-status Report
  • Research Products

    (6 results)

All 2014 2012 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (4 results) Remarks (1 results)

  • [Journal Article] GLI1 modulates EMT in pancreatic cancer-Letter2012

    • Author(s)
      Shingo Inaguma, Kenji Kasai, Mitsuyoshi Hashimoto, Hiroshi Ikeda
    • Journal Title

      Cancer Research

      Volume: (in press) Issue: 14 Pages: 3702-3

    • DOI

      10.1158/0008-5472.can-12-0379

    • Related Report
      2012 Research-status Report
    • Peer Reviewed
  • [Presentation] ヘッジホッグシグナル系転写因子ZIC2はFGFR3, ANXA8L2発現誘導を介して膵発がんを促進する2014

    • Author(s)
      稲熊真悟, ら
    • Organizer
      第103回日本病理学会総会
    • Place of Presentation
      広島
    • Year and Date
      2014-04-25
    • Related Report
      2013 Final Research Report
  • [Presentation] ZIC2 is an indispensable transcription factor for the cell growth of pancreatic ductal adenocarcinoma2014

    • Author(s)
      Shingo INAGUMA, et.al
    • Organizer
      USCAP 2014 annual meeting
    • Place of Presentation
      San Diego
    • Year and Date
      2014-03-04
    • Related Report
      2013 Final Research Report
  • [Presentation] ZIC2 is an indispensable transcription factor for the cell growth of pancreatic ductal adenocarcinoma.2014

    • Author(s)
      Shingo Inaguma, Kenji Kasai, Mitsuyoshi Hashimoto, Miho Riku, Hiroshi Ikeda.
    • Organizer
      USCAP 2014, annual meeting.
    • Place of Presentation
      San Diego, CA.
    • Related Report
      2013 Annual Research Report
  • [Presentation] ヘッジホッグシグナル系転写因子ZIC2はFGFR3, ANXA8L2発現誘導を介して膵発癌を促進する2014

    • Author(s)
      稲熊真悟、笠井謙次、橋本光義、陸美穂、池田洋
    • Organizer
      第103回 日本病理学会総会
    • Place of Presentation
      広島
    • Related Report
      2013 Annual Research Report
  • [Remarks]

    • URL

      http://www.aichi-med-u.ac.jp/univ/medic/lecture2/10.html

    • Related Report
      2011 Research-status Report

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Published: 2011-08-05   Modified: 2019-07-29  

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