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Screening for the suppressor of the expression of thymidylate synthase

Research Project

Project/Area Number 24659305
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Hygiene
Research InstitutionKyoto Prefectural University of Medicine

Principal Investigator

SOWA Yoshihiro  京都府立医科大学, 医学(系)研究科(研究院), 准教授 (70315935)

Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2012: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywordsthymidylate synthase / fenofibrate / PI3K阻害剤 / PI3K/Akt経路 / MAPK経路
Research Abstract

Since the activity of thymidylate synthase (TS) is essential for cell proliferation, the expression of TS is higher in various cancer cells than in normal cells. Therefore, we tried to find the suppressors of the expression of TS for cancer prevention. As the results, we found that fenofibrate, which is used to reduce cholesterol levels, reduced the expression of TS in human colon cancer HT-29 cells and that LY294002, a PI3K inhibitor, also reduced it in human colon cancer HCT15 cells. These results raise a possibility that these compounds might be useful for the treatment and prevention against colon cancer.

Report

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

    (6 results)

All 2013 Other

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

  • [Journal Article] Novel MEK inhibitor trametinib and other retinoblastoma gene (RB)-reactivating agents enhance efficacy of 5-fluorouracil on human colon cancer cells2013

    • Author(s)
      Watanabe M, Sowa Y, Yogosawa M, Sakai T.
    • Journal Title

      Cancer Sci.

      Volume: Epub ahead of print Issue: 6 Pages: 687-693

    • DOI

      10.1111/cas.12139

    • Related Report
      2013 Annual Research Report 2013 Final Research Report
    • Peer Reviewed
  • [Presentation] Novel MEK inhibitor trametinib and other RB-reactivating agents enhance efficacy of 5-fluorouracil on human colon cancer cells2013

    • Author(s)
      Motoki Watanabe, Yoshihiro Sowa, Toshiyuki Sakai
    • Organizer
      日本癌学会学術集会
    • Place of Presentation
      横浜
    • Year and Date
      2013-10-03
    • Related Report
      2013 Final Research Report
  • [Presentation] 新規MEK阻害剤trametinibなどによるRB再活性化により大腸癌細胞に対する5-FU感受性が増強される2013

    • Author(s)
      渡邉元樹、曽和義広、酒井敏行
    • Organizer
      日本がん分子標的治療学会学術集会
    • Place of Presentation
      京都
    • Year and Date
      2013-06-14
    • Related Report
      2013 Final Research Report
  • [Presentation] 新規MEK阻害剤trametinibなどによるRB再活性化により大腸癌細胞株に対する5-FU感受性が増強される

    • Author(s)
      渡邉元樹、曽和義広、酒井敏行
    • Organizer
      日本がん分子標的治療学会学術集会
    • Place of Presentation
      横浜
    • Related Report
      2013 Annual Research Report
  • [Presentation] Novel MEK inhibitor trametinib and RB-reactivating agents enhance efficiency of 5-Fluorouracil on human colon cancer cells

    • Author(s)
      Motoki Watanabe, Yoshihiro Sowa, Toshiyuki Sakai
    • Organizer
      日本癌学会学術総会
    • Place of Presentation
      京都
    • Related Report
      2013 Annual Research Report
  • [Remarks]

    • URL

      http://www.f.kpu-m.ac.jp/k/pubmed/

    • Related Report
      2013 Final Research Report

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

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