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Functional analysis of the novel metastasis-promoting factor Merm1

Research Project

Project/Area Number 25890022
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Tumor biology
Research InstitutionJapanese Foundation for Cancer Research

Principal Investigator

TAKEMOTO Ai  公益財団法人がん研究会, がん化学療法センター, 研究員 (20706494)

Project Period (FY) 2013-08-30 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywordsがん転移
Outline of Final Research Achievements

Merm1 is a metastasis-promoting factor isolated from in vivo screening. We performed the analysis of Merm1 to elucidate the mechanism of Merm1-regulated metastasis and to propose the new target for metastasis therapy. We found Merm1 MTase domain related to invasion ability of Merm1-expressing high metastatic cells. We searched Merm1-interactants and identified the conserved component of Merm1-holo complex and the ubiquitinylation enzymes which possibly regulate Merm1. And we observed that the some population of nuclear Merm1 localized in a nucleolus and Merm1 level and its MTase domain affected nucleolus morphology. Further analysis of the relationship between the interactants, the function in nucleolus and metastasis regulation by Merm1 is required.

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Annual Research Report
  • Research Products

    (6 results)

All 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (4 results) Book (1 results)

  • [Journal Article] Platelets promote osteosarcoma cell growth through activation of the PDGFR-Akt signaling axis.2014

    • Author(s)
      Satoshi Takagi, Ai Takemoto, Miho Takami, Tomoko Oh-hara, and Naoya Fujita
    • Journal Title

      Cancer Sci.

      Volume: 105 Issue: 8 Pages: 983-988

    • DOI

      10.1111/cas.12464

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Presentation] Aggrus依存的な血小板凝集はEMTを介してがん転移を促進する2015

    • Author(s)
      竹本愛、 大原智子、 藤田直也
    • Organizer
      第19回日本がん分子標的治療学会学術集会
    • Place of Presentation
      松山
    • Year and Date
      2015-06-10 – 2015-06-12
    • Related Report
      2014 Annual Research Report
  • [Presentation] Aggrus-induced platelet aggregation promotes tumor metastasis by enhancing EMT2015

    • Author(s)
      Ai Takemoto, Satoshi Takagi, Mina Okitaka, Miho Takami, Shigeo Sato, Tomoko Oh-hara, and Naoya Fujita
    • Organizer
      Joint International Symposium on TGF-beta Family and Cancer Signal Network in Tumor Microenvironment
    • Place of Presentation
      Tsukuba
    • Year and Date
      2015-01-12 – 2015-01-13
    • Related Report
      2014 Annual Research Report
  • [Presentation] 血小板はPDGFR-Akt経路活性化を介して骨肉腫の悪性化に寄与する2014

    • Author(s)
      竹本愛、高木聡、高見美穂、大原智子、藤田直也
    • Organizer
      第73回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2014-09-25 – 2014-09-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] 血小板はPDGFR-Akt経路活性化を介して骨肉腫の悪性化に寄与する2014

    • Author(s)
      竹本愛、高木聡、高見美穂、大原智子、藤田直也
    • Organizer
      平成26年度がん若手研究者ワークショップ
    • Place of Presentation
      蓼科
    • Year and Date
      2014-09-03 – 2014-09-06
    • Related Report
      2014 Annual Research Report
  • [Book] 実験医学増刊 がん微小環境と標的治療、第4章-5. がん悪性化に関わる血小板の凝集機構を標的とした治療2015

    • Author(s)
      竹本愛、藤田直也
    • Total Pages
      6
    • Publisher
      羊土社
    • Related Report
      2014 Annual Research Report

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Published: 2013-09-12   Modified: 2019-07-29  

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