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2011 Fiscal Year Final Research Report

Basic research on personalized treatment of cancer by HDAC inhibitors

Research Project

  • PDF
Project/Area Number 21590166
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Medical pharmacy
Research InstitutionNagasaki University

Principal Investigator

OZAKI Kei-ichi  長崎大学, 大学院・医歯薬学総合研究科, 准教授 (50252466)

Research Collaborator 坂元 利彰  , 大学院生
藤尾 康祐  , 大学院生
梶川 修平  , 大学院生
Project Period (FY) 2009 – 2011
Keywordsオーダーメード医療
Research Abstract

Histone deacetylase(HDAC) inhibitors which are promising anti-tumor agents have high selectivity to the cancer cell in which the ERK-MAP kinase pathway is constitutively activated. The molecular mechanism which results in remarkable HDAC inhibitor sensitivity by blockade of this pathway with MEK inhibitors was clarified. Moreover, in vitro and the animal experiment with xenograft model proved that it is effective also in the cancers which are resistant to some molecular-targeted drugs such as tyrosine kinase inhibitors. It is expected that these results will be useful for the personalized treatment of cancer by HDAC inhibitors.

  • Research Products

    (12 results)

All 2011 2010 2009

All Journal Article (4 results) Presentation (8 results)

  • [Journal Article] Targeting the extracellular signal-regulated kinase pathway in cancer therapy2011

    • Author(s)
      M. Kohno, S. Tanimura, and K. Ozaki
    • Journal Title

      Biol. Pharm. Bull

      Volume: 34 Pages: 1781-1784

  • [Journal Article] Blockade of the extracellular signal-regulated kinase pathway enhances the therapeutic efficacy of microtubule-destabilizing agents in human tumor xenograft models2010

    • Author(s)
      K. Watanabe, S. Tanimura, A. Uchiyama, T. Sakamoto, T. Kawabata, K. Ozaki, and M. Kohno
    • Journal Title

      Clin. Cancer Res

      Volume: 16 Pages: 1170-1178

  • [Journal Article] Blockade of the ERK or PI3K-Akt pathway enhances the cytotoxicity of histone deacetylase inhibitors in tumor cells resistant to gefitinib or imatinib2010

    • Author(s)
      K. Ozaki, M. Kosugi, N. Baba, T. Sakamoto, K. Fujio, S. Kimura and M. Kohno
    • Journal Title

      Biochem. Biophys. Res. Commun

      Volume: 391 Pages: 1610-1615

  • [Journal Article] Blockade of constitutively activated ERK signaling enhances cytotoxicity of microtubule-destabilizing agents in tumor cells2009

    • Author(s)
      S. Tanimura, A. Uchiyama, K. Watanabe, M. Yasunaga, T. Kawabata, K. Ozaki and M. Kohno
    • Journal Title

      Biochem. Biophys. Res. Commun

      Volume: 378 Pages: 650-655

  • [Presentation] ERK経路の活性化及びp53遺伝子型とHDAC阻害剤感受性の相関2011

    • Author(s)
      梶川修平, 坂元利彰, 尾崎惠一, 河野通明
    • Organizer
      第34回日本分子生物学会年会
    • Place of Presentation
      横浜
    • Year and Date
      20111200
  • [Presentation] HC-toxin and PD184352 synergistically up-regulate Bim and TBP-2 to induce the enhanced ROS accumulation and cell death2011

    • Author(s)
      K, Ozaki, K, Fujio, T, Sakamoto, S, Kajikawa, and M, Kohno
    • Organizer
      第70回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Year and Date
      20111000
  • [Presentation] HDAC阻害剤とMEK阻害剤の併用による細胞死誘導増強-FOXO転写因子ファミリーの役割2010

    • Author(s)
      藤尾康祐, 梶川修平, 坂元利彰, 尾崎惠一, 河野通明
    • Organizer
      第27回日本薬学会九州支部大会
    • Place of Presentation
      長崎
    • Year and Date
      20101200
  • [Presentation] Blockade of the ERK pathway enhances the therapeutic efficacy of HDAC inhibitors in human tumor xenograft models2010

    • Author(s)
      T. Sakamoto, K. Fujio, S. Kajikawa, S. Uesato, K. Watanabe, S. Tanimura, K. Ozaki, M. Kohno
    • Organizer
      第69回日本癌学会学術総会
    • Place of Presentation
      大阪
    • Year and Date
      20101000
  • [Presentation] がん細胞におけるERK経路活性化とHDAC阻害剤感受性の相関2010

    • Author(s)
      梶川修平, 坂元利彰, 藤尾康祐, 尾崎惠一, 河野通明
    • Organizer
      第9回次世代を担う若手ファーマ・バイオフォーラム2010
    • Place of Presentation
      京都
    • Year and Date
      20100900
  • [Presentation] MEK阻害剤とHDAC阻害剤の併用による抗腫瘍効果増強-xenograftでの検討2009

    • Author(s)
      坂元利彰, 藤尾康祐, 梶川修平, 尾崎惠一, 河野通明
    • Organizer
      第26回日本薬学会九州支部大会
    • Place of Presentation
      福岡
    • Year and Date
      20091200
  • [Presentation] イマチニブ抵抗性Bcr-Abl変異(T315I)白血病細胞に対する効果的治療法の開発2009

    • Author(s)
      馬場伸幸, 尾崎惠一, 河野通明
    • Organizer
      第26回日本薬学会九州支部大会
    • Place of Presentation
      福岡
    • Year and Date
      20091200
  • [Presentation] HDAC阻害剤とMEK阻害剤の併用による細胞死増強の分子機構2009

    • Author(s)
      坂元利彰, 尾崎惠一, 馬場伸幸, 藤尾康祐, 梶川修平, 河野通明
    • Organizer
      第18回日本アポトーシス研究会学術集会
    • Place of Presentation
      長崎
    • Year and Date
      20090800

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Published: 2013-07-31  

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