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Development of novel therapeutic agents for malignant peripheral nerve sheath tumor

Research Project

Project/Area Number 15K18436
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Tumor therapeutics
Research InstitutionTohoku University

Principal Investigator

Saijo Ken  東北大学, 大学病院, 助教 (70636729)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords悪性末梢神経鞘腫 / 軟部肉腫 / HDAC / PI3K / 創薬 / 分子標的薬
Outline of Final Research Achievements

Malignant peripheral nerve sheath tumor (MPNST) is a histologic subtype of soft tissue sarcoma. Patients with advanced soft tissue sarcoma including MPNST have poor prognosis and no effective therapeutic drugs, so that development of novel therapeutic drugs is awaited. We have found that depsipeptide analogs inhibit cancer cell proliferation with a mechanism of dual inhibition of HDAC and PI3K, both of which are regarded as molecular targets for soft tissue sarcoma therapy. In this study, the effects of depsipeptide analogs were evaluated using MPNST cell lines and a fibrosarcoma cell line. Because the proliferation rate of MPNST cells was slow and it was difficult to establish an experimental system by a mouse model, experiments were carried out using a fibrosarcoma cell line. We showed antitumor effect and the mechanism of action of HDAC/PI3K dual inhibition of the depsipeptide analog in fibrosarcoma tumor tissue.

Report

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

    (5 results)

All 2017 2016 2015

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results,  Acknowledgement Compliant: 1 results) Presentation (3 results) (of which Int'l Joint Research: 2 results) Funded Workshop (1 results)

  • [Journal Article] Antitumor activity and pharmacologic characterization of the depsipeptide analog as a novel HDAC/PI3K dual inhibitor.2017

    • Author(s)
      Saijo K, Imai H, Chikamatsu S, Narita K, Katoh T, Ishioka C.
    • Journal Title

      Cancer Science

      Volume: 印刷中 Issue: 7 Pages: 1469-1475

    • DOI

      10.1111/cas.13255

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Presentation] Evaluation of anti-tumor effects of depsipeptide analogs as HDAC/PI3K dual inhibitors in human soft tissue sarcoma cells2016

    • Author(s)
      Ken SAIJO, Koichi NARITA, Tadashi KATOH, and Chikashi ISHIOKA
    • Organizer
      日本癌学会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2016-10-06
    • Related Report
      2016 Annual Research Report
    • Int'l Joint Research
  • [Presentation] In vivo anti-tumor activity of FK-A11, a depsipeptide analog targeting both histone deacetylase and phosphoinositide 3-kinase2015

    • Author(s)
      Ken Saijo, Koichi Narita, Tadashi Katoh, and Chikashi Ishioka
    • Organizer
      ESMO Asia
    • Place of Presentation
      singapore, Singapore
    • Year and Date
      2015-12-19
    • Related Report
      2015 Research-status Report
    • Int'l Joint Research
  • [Presentation] Characterization of depsipeptide analogs as PI3K inhibitors2015

    • Author(s)
      Ken SAIJO, Koichi NARITA, Tadashi KATOH, and Chikashi ISHIOKA
    • Organizer
      日本癌学会学術総会
    • Place of Presentation
      名古屋, 名古屋国際会議場
    • Year and Date
      2015-10-10
    • Related Report
      2015 Research-status Report
  • [Funded Workshop] ESMO Asia 20152015

    • Place of Presentation
      singapore, Singapore
    • Year and Date
      2015-12-18
    • Related Report
      2015 Research-status Report

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Published: 2015-04-16   Modified: 2018-03-22  

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