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Tumoral immune escape mechanism in malignant glioma

Research Project

Project/Area Number 26870237
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Immunology
Neurosurgery
Research InstitutionUniversity of Yamanashi

Principal Investigator

MITSUKA Kentaro  山梨大学, 総合研究部, 医学研究員 (70402071)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2016: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywordsグリオーマ / 免疫療法 / トリプトファン / キヌレニン / インドールアミン2,3ジオキシゲナーゼ / インドールアミン2,3ジオキシゲナーゼ / テモゾロミド / Indoleamine dioxigenase / malignant glioma / T-reg / temozolomide / 1-MT / トリプトファン代謝酵素 / IDO
Outline of Final Research Achievements

Indoleamine 2,3-dioxygenase (IDO), a key enzyme of tryptophan (Trp) metabolism, is involved in tumor-derived immune suppression by depleting Trp and accumulating the metabolite. We have recently shown that IDO expression was markedly increased in human glioblastoma and secondary glioblastoma with malignant change. The aim of this study is to investigate anti-tumor effect of IDO inhibition and to search the synergistic function of IDO inhibitor (1-MT) and temozolomide in a murine glioma model. In subcutaneous model, oral administration of 1-MT significantly suppressed tumor growth and synergistic anti-tumor effects of 1-MT and temozolomide were observed (P<0.01). The mice intracranially inoculated IDO knockdown cells had a significantly longer survival compared to the control mice (P<0.01). The mice intracranially inoculated IDO knockdown cells had a significantly longer survival compared to the control mice (P<0.01).

Report

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

    (5 results)

All 2016 2014 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (3 results) (of which Int'l Joint Research: 1 results) Remarks (1 results)

  • [Journal Article] Synergistic anti-tumor effect with indoleamine 2,3-dioxygenase inhibition and temozolomide in a murine glioma model.2016

    • Author(s)
      1.Hanihara M, Kawataki T, Oh-oka K, Mitsuka K, Nakao A, and Kinouchi H
    • Journal Title

      Journal of Neurosurgery

      Volume: in printing Issue: 6 Pages: 1594-1601

    • DOI

      10.3171/2015.5.jns141901

    • Related Report
      2016 Annual Research Report 2015 Research-status Report
    • Peer Reviewed
  • [Presentation] Synergistic anti-tumor effect with Indoleamine 2,3-dioxygenase inhibition and Temozolomide in a murine glioma model2016

    • Author(s)
      Mitsuto Hanihara, Tomoyuki Kawataki, Hiroyuki Kinouchi
    • Organizer
      Tumor section satellite symposium, CNS Annual Meeting 2016
    • Place of Presentation
      米国、サンディエゴ
    • Year and Date
      2016-09-24
    • Related Report
      2016 Annual Research Report
    • Int'l Joint Research
  • [Presentation] 悪性グリオーマと免疫療法:トリプトファン代謝酵素Indoleamine 2, 3- dioxygenase (IDO)の抑制とテモゾロミドの併用効果2016

    • Author(s)
      埴原 光人、川瀧 智之、大岡 杏子、中尾 篤人、木内 博之
    • Organizer
      第11回 脳腫瘍の基礎シンポジウム
    • Place of Presentation
      東京、千代田区
    • Year and Date
      2016-05-14
    • Related Report
      2016 Annual Research Report
  • [Presentation] マウスグリオーマモデルにおけるインドールアミン2,3ジオキシゲナーゼ阻害による抗腫瘍効果2014

    • Author(s)
      埴原光人、川瀧智之、三塚健太郎、大岡杏子、荻原雅和、中尾篤人、木内博之
    • Organizer
      一般社団法人日本脳神経外科学会 第73回学術総会
    • Place of Presentation
      グランドプリンスホテル新高輪 (東京・港区)
    • Year and Date
      2014-10-09 – 2014-10-11
    • Related Report
      2014 Research-status Report
  • [Remarks] 山梨大学医学部附属病院 脳神経外科 講座紹介

    • URL

      http://www.med.yamanashi.ac.jp/clinical/neurosur/html/course-info/index.html

    • Related Report
      2016 Annual Research Report

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

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