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Analysis of cancer relapse mechanisms by proteomic profiling using drug-tolerant cell subpopulation

Research Project

Project/Area Number 25830121
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Tumor therapeutics
Research InstitutionIwate Medical University

Principal Investigator

KUME Kohei  岩手医科大学, 医学部, ポストドクター (10609663)

Project Period (FY) 2013-04-01 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywords抗癌剤耐性 / 癌性腹膜炎 / RNAポリメラーゼ / 逆相タンパク質マイクロアレイ / RNAポリメラーゼII / TAF15 / 薬剤寛容性細胞集団 / コロニー形成 / シスプラチン
Outline of Final Research Achievements

Cancer relapse is often seen even after curative operation followed by adjuvant chemotherapy. In this study, we analyzed cancer cell colonies that emerge in the presence of anticancer drugs (drug-tolerant colonies, DTCs) as a cancer relapse model. Proteomic characterization of DTCs identified two major subgroups, but none of these characters associated with DTCs. A lead compound screening identified an RNA polymerase inhibitor (RNAPi) bearing potency in DTC suppression. RNAPi with cisplatin significantly reduced the number of nodules of peritoneal dissemination of gastric cancer in mice. These findings suggest that RNAPi is potent in suppression of cancer relapse such as peritoneal dissemination of gastric cancer.

Report

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

    (13 results)

All 2014 2013 Other

All Journal Article (2 results) (of which Peer Reviewed: 2 results) Presentation (9 results) Remarks (2 results)

  • [Journal Article] A Compensatory Role of NF-κB to p53 in Response to 5-FU–Based Chemotherapy for Gastric Cancer Cell Lines2013

    • Author(s)
      Fumitaka Endo
    • Journal Title

      PLoS ONE

      Volume: 9

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Journal Article] Chitin and Chitosan (DAC-70) -Biomedical Application-2013

    • Author(s)
      Akio Sugitachi
    • Journal Title

      Chitin and Chitosan Tesearch

      Volume: 19 Pages: 12-15

    • Related Report
      2013 Research-status Report
    • Peer Reviewed
  • [Presentation] Inhibition of RNA Pol II suppresses the emergence of drug-tolerant cell subpopulations.2014

    • Author(s)
      久米浩平, 西塚哲, 遠藤史隆, 片桐弘勝, 前沢千早, 若林剛.
    • Organizer
      第73回日本癌学会学術総会
    • Place of Presentation
      横浜
    • Year and Date
      2014-09-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] Emergence of bimodal responses to etoposide in human cancer cell lines.2014

    • Author(s)
      久米浩平, 西塚哲, 若林剛.
    • Organizer
      The 15th International Conference on Systems Biology
    • Place of Presentation
      コペンハーゲン
    • Year and Date
      2014-09-15
    • Related Report
      2014 Annual Research Report
  • [Presentation] コロニー形成試験を用いた薬剤寛容性細胞集団の分子プロファイリング2014

    • Author(s)
      久米浩平, 西塚哲, 池田めぐみ, 三浦佐和子, 若林剛.
    • Organizer
      未来医療開発プロジェクトシンポジウム
    • Place of Presentation
      盛岡
    • Year and Date
      2014-08-07
    • Related Report
      2014 Annual Research Report
  • [Presentation] Imaging cytometric analysis of cancer cell subpopulation accumulating p53 in the nucleous in response to etoposide.2014

    • Author(s)
      久米浩平, 西塚哲, 前沢千早, 若林剛.
    • Organizer
      37th The Naito Conference
    • Place of Presentation
      ニセコ
    • Year and Date
      2014-07-15 – 2014-07-18
    • Related Report
      2014 Annual Research Report
  • [Presentation] Imaging cytometric analysis of cancer cell subpopulation accumulating p53 in response to etoposide2014

    • Author(s)
      Kohei Kume
    • Organizer
      The 37th Naito Conference
    • Place of Presentation
      Niseko
    • Related Report
      2013 Research-status Report
  • [Presentation] Transcriptional and proteomic profiling of drug-tolerant cancer cell subpopulations using colonies that emerge in the presence of anticancer agents2014

    • Author(s)
      Kohei Kume
    • Organizer
      AACR2014
    • Place of Presentation
      San Diego
    • Related Report
      2013 Research-status Report
  • [Presentation] Genotoxic drug-induced switch-like protein expression of nuclear p53 in human cancer cells2013

    • Author(s)
      Kohei Kume
    • Organizer
      ICSB2013
    • Place of Presentation
      Copenhagen
    • Related Report
      2013 Research-status Report
  • [Presentation] Analysis of drug-tolerant phenotype by molecular profiling of single colonies2013

    • Author(s)
      Kohei Kume
    • Organizer
      JCA2013
    • Place of Presentation
      Yokohama
    • Related Report
      2013 Research-status Report
  • [Presentation] Analysis of cancer cell populations by isolated single colonies for the identification of drug-tolerance inducing factor2013

    • Author(s)
      Kohei Kume
    • Organizer
      AACR2013
    • Place of Presentation
      Washington, DC
    • Related Report
      2013 Research-status Report
  • [Remarks] Nishizuka Lab at Depertment of Surgery

    • URL

      http://www.nishizukalab.org/

    • Related Report
      2014 Annual Research Report
  • [Remarks] Nishizuka Lab Education

    • URL

      https://www.facebook.com/pages/Nishizuka-Lab/329548837116478

    • Related Report
      2014 Annual Research Report

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Published: 2014-07-25   Modified: 2019-07-29  

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