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Development of molecular target therapy using new angiogenin inhibitor against cancer induced bone diseases

Research Project

Project/Area Number 23390463
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Surgical dentistry
Research InstitutionOkayama University

Principal Investigator

SASAKI AKIRA  岡山大学, 医歯(薬)学総合研究科, 教授 (00170663)

Co-Investigator(Kenkyū-buntansha) SHIMO Tsuyoshi  岡山大学, 大学院・医歯薬学総合研究科, 准教授 (40362991)
KISHIMOTO Koji  岡山大学, 大学院・医歯薬学総合研究科, 助教 (40243480)
IBARAGI Souitiro  岡山大学病院, 助教 (80549866)
YOSHIOKA Norie  岡山大学, 大学院・医歯薬学総合研究科, 助教 (50362984)
Project Period (FY) 2011-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥12,870,000 (Direct Cost: ¥9,900,000、Indirect Cost: ¥2,970,000)
Fiscal Year 2013: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
Fiscal Year 2012: ¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2011: ¥6,500,000 (Direct Cost: ¥5,000,000、Indirect Cost: ¥1,500,000)
Keywordsangiogenin / neomycine / 口腔扁平上皮癌 / 骨浸潤 / 癌誘発骨破壊 / 血管新生因子 / 破骨細胞 / 血管新生阻害薬 / angionenin / 骨破壊モデル / ノックアウトマウス / 骨破壊 / 癌 / 骨吸収
Research Abstract

Osteoclast-mediated bone resorption plays an important role in bone invasion or bone destruction of the cancer. We have been establishing the treatment of the cancer induced-bone diseases which assumed angiogenesis factor, angiogenin (ANG) as a molecular target.
In the present study, we examined a therapeutic utility of ANG inhibitor and investigated the role of ANG using ANG-1 knockout mouse (ANG-KO). Trabecular bone formation of the early period of growth was suppressed in ANG-KO compare to the wild type mice (WT), and the in vitro osteoclasts formation using cells of ANG-KO was inhibited, but there were few differences in vivo model. The ANG inhibitor was able to confirm a utility for a mouse cancer bone destruction model. Newly developed medicine, Terrein, which inhibit the production of ANG, had not only the inhibition of angiogenesis, but also the antitumor activity. Therefore, a utility of ANG inhibitors against the cancer induced bone diseases was suggested.

Report

(4 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Annual Research Report
  • 2011 Annual Research Report
  • Research Products

    (5 results)

All 2014 2013 2012 2011

All Journal Article (2 results) (of which Peer Reviewed: 1 results) Presentation (3 results)

  • [Journal Article] Neamine inhibits oral cancer progression by suppressing angiogenin-mediated angiogenesis and cancer cell proliferation2014

    • Author(s)
      Koji Kishimoto, Shoko Yoshida, Soichiro Ibaragi, Norie Yoshioka, Guo-Fu Hu, Akira Sasaki
    • Journal Title

      Anticancer Research

      Volume: 34 Pages: 2113-2122

    • URL

      http://www.ncbi.nlm.nih.gov/pubmed/24778013

    • Related Report
      2013 Final Research Report
    • Peer Reviewed
  • [Journal Article] 血管新生因子angiogeninを標的とした口腔扁平上皮癌の癌骨破壊制御に関する研究2012

    • Author(s)
      青木香澄
    • Journal Title

      岡山歯学会雑誌

      Volume: 31

    • Related Report
      2012 Annual Research Report
  • [Presentation] Neamine の口腔癌に対する抗腫瘍効果の検討2013

    • Author(s)
      岸本晃治, 他
    • Organizer
      第31回日本口腔腫瘍学会総会・学術大会
    • Place of Presentation
      東京
    • Year and Date
      2013-01-24
    • Related Report
      2013 Final Research Report
  • [Presentation] Neamine inhibits progression of oral cancer by suppressing angiogenin-stimulated angiogenesis and cancer cell proliferation2012

    • Author(s)
      岸本晃治, 他
    • Organizer
      21 Congress of the European Association for Cranio-Maxillo-Facial Surgery
    • Place of Presentation
      Dubrovnik (Croatia)
    • Related Report
      2013 Final Research Report
  • [Presentation] Angiogeninの発現亢進は口腔癌の増殖と進展に関与する2011

    • Author(s)
      岸本晃治, 他
    • Organizer
      第29回日本口腔腫瘍学会総会・学術大会
    • Place of Presentation
      熊本
    • Year and Date
      2011-01-27
    • Related Report
      2013 Final Research Report

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Published: 2011-04-06   Modified: 2019-07-29  

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