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Development of cancer prevention based on the molecular mechanism against malignant mesothelioma.

Research Project

Project/Area Number 21390192
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Hygiene
Research InstitutionKyoto Prefectural University of Medicine

Principal Investigator

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

Co-Investigator(Kenkyū-buntansha) TOMOSUGI Mano (HORINKA Mano)  京都府立医科大学, 医学研究科, 助教 (80512037)
Project Period (FY) 2009 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥17,160,000 (Direct Cost: ¥13,200,000、Indirect Cost: ¥3,960,000)
Fiscal Year 2012: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2011: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2010: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2009: ¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Keywords悪性中皮腫 / DNA メチル化 / microRNA / HDAC 阻害剤 / DNAメチル化 / HDAC阻害剤 / Reactive oxygen species (ROS) / ミトコンドリア / Reactive oxygen species(ROS) / グルタチオン / アポトーシス
Research Abstract

In malignant mesothelioma cells, miR-34b/c, which is known as a tumor suppressive microRNA, is suppressed by DNA methylation. Since the combination treatment of DNA methyltransferase inhibitor and histone deacetylase (HDAC) inhibitor abrogated the DNA methylation, we treated malignant mesothelioma cells with the combination. As a result, the combination induced growth arrest, apoptosis and the upregulation of miR-34b/c. These results raise a possibility that the combination treatment of DNA methyltransferase inhibitor and HDAC inhibitor might be useful for the treatment and prevention against malignant mesothelioma.

Report

(5 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Annual Research Report
  • 2010 Annual Research Report
  • 2009 Annual Research Report
  • Research Products

    (8 results)

All 2010 Other

All Journal Article (2 results) (of which Peer Reviewed: 1 results) Presentation (2 results) Remarks (4 results)

  • [Journal Article] Histone deacetylase inhibitors and 15-deoxy-Δ^<12,14>-prostaglandin J_2 synergistically induce apoptosis.2010

    • Author(s)
      Koyama M, et al.
    • Journal Title

      Clinical Cancer Research

      Volume: 16(8) Pages: 2320-2332

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Journal Article] HDAC阻害剤の開発状況2010

    • Author(s)
      曽和義広
    • Journal Title

      癌と化学療法

      Volume: 37(9) Pages: 1665-1668

    • Related Report
      2010 Annual Research Report
  • [Presentation] HDAC阻害剤と15-deoxy-Δ^<12,14>-prostaglandin J_2の併用療法は相乗的にアポトーシスを引き起こす2010

    • Author(s)
      小山真, 他
    • Organizer
      日本がん分子標的治療学会
    • Place of Presentation
      東京
    • Year and Date
      2010-07-08
    • Related Report
      2010 Annual Research Report
  • [Presentation] Histone deacetylase inhibitors and 15-deoxy-Δ^<12,14>-prostaglandin J_2 synergistically induce apoptosis.2010

    • Author(s)
      Koyama M, et al.
    • Organizer
      American Association for Cancer Research
    • Place of Presentation
      Washington D.C., U.S.A
    • Year and Date
      2010-04-21
    • Related Report
      2010 Annual Research Report
  • [Remarks]

    • URL

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

    • Related Report
      2012 Final Research Report
  • [Remarks]

    • URL

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

    • Related Report
      2011 Annual Research Report
  • [Remarks]

    • URL

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

    • Related Report
      2010 Annual Research Report
  • [Remarks]

    • URL

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

    • Related Report
      2009 Annual Research Report

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Published: 2009-04-01   Modified: 2019-07-29  

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