• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Establishment of an novel reversal of anticancer drug resistance based on the epigenetic information

Research Project

Project/Area Number 26460246
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Medical pharmacy
Research InstitutionHimeji Dokkyo University

Principal Investigator

Takara Kohji  姫路獨協大学, 薬学部, 教授 (00329939)

Co-Investigator(Kenkyū-buntansha) 峯垣 哲也  京都薬科大学, 薬学部, 助教 (10549306)
木下 淳  姫路獨協大学, 薬学部, 講師 (60454766)
中山 優子  姫路獨協大学, 薬学部, 助手 (50708419)
Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywordsエピジェネティクス / 癌 / 抗癌剤耐性
Outline of Final Research Achievements

The various types of mechanism are participated in the phenomena which shows the resistance to anticancer drugs in cancer cells. Herein, from the viewpoints of epigenetics causing the change in the gene function, the relation with the drug resistance and epigenetics were examined. As results, the differences in the global DNA methylation were not found in HeLa and its resistant cells. However, the expressions of mRNA involving in the epigenetics were different among the cells. Treatment with drugs having the activity of demethylation increased sensitivity to cisplatin in either cells. Consequently, the novel possibility of reversal of resistance may be demonstrated, although the relation with the drug resistance and epigenetics has not reached the sufficient evidence.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • Research Products

    (6 results)

All 2016 2015

All Presentation (6 results)

  • [Presentation] ABCB5発現抑制によるシスプラチン耐性の誘導2016

    • Author(s)
      中山優子、木下 淳、峯垣哲也、山本和宏、髙良恒史
    • Organizer
      日本薬学会第136年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2016-03-26
    • Related Report
      2015 Research-status Report
  • [Presentation] アミノ酸トランスポーターの発現と抗癌剤耐性との関連性2016

    • Author(s)
      中山優子、木下 淳、峯垣哲也、山本和宏、髙良恒史
    • Organizer
      日本薬学会第136年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2016-03-26
    • Related Report
      2015 Research-status Report
  • [Presentation] アミノ酸トランスポーターを標的としたシスプラチン耐性の克服2015

    • Author(s)
      中山優子、深澤郁也、木下 淳、峯垣哲也、山本和宏、髙良恒史
    • Organizer
      第25回日本医療薬学会年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2015-11-21
    • Related Report
      2015 Research-status Report
  • [Presentation] アキシチニブで長期曝露したヒト腎臓癌由来Caki-2の細胞特性2015

    • Author(s)
      中山優子、山本和宏、峯垣哲也、木下 淳、髙良恒史
    • Organizer
      日本薬学会第135年会
    • Place of Presentation
      デザイン・クリエイティブセンター神戸
    • Year and Date
      2015-03-26 – 2015-03-28
    • Related Report
      2014 Research-status Report
  • [Presentation] Poly (ADP-ribose) polymerase阻害剤Veliparib耐性ヒト乳癌細胞株の樹立とその特性2015

    • Author(s)
      山本 彩佳, 峯垣 哲也, 棚橋 真実, 宮本 恵輔, 荒木 悠, 稲垣 恵未, 林 絵里, 伊藤 恵, 吉本 咲貴, 中山 優子, 高良 恒史, 辻本 雅之, 西口 工司
    • Organizer
      日本薬学会第135年会
    • Place of Presentation
      デザイン・クリエイティブセンター神戸
    • Year and Date
      2015-03-26 – 2015-03-28
    • Related Report
      2014 Research-status Report
  • [Presentation] 腎細胞癌におけるスニチニブ不応性および耐性メカニズムの探索2015

    • Author(s)
      水本 篤志, 山本 和宏, 高良 恒史, 中山 優子, 中川 勉, 平野 剛, 平井 みどり
    • Organizer
      日本薬学会第135年会
    • Place of Presentation
      神戸学院大学
    • Year and Date
      2015-03-26 – 2015-03-28
    • Related Report
      2014 Research-status Report

URL: 

Published: 2014-04-04   Modified: 2018-03-22  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi