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Development research of molecular targeted therapy for oral cancer mediated by ubiquitin ligase inhibitor

Research Project

Project/Area Number 26893166
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Surgical dentistry
Research InstitutionHiroshima University

Principal Investigator

SAKAUE TAISHI  広島大学, 大学病院, 歯科診療医 (00735160)

Project Period (FY) 2014-08-29 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords口腔癌 / インテグリン / ユビキチンリガーゼ
Outline of Final Research Achievements

It was revealed that HDM2 was the ubiquitin ligase which regulated the ubiquitination of integrin beta 8 by binding to EGF-like repeat domains in integrin beta 8 subunit leg. Treatment of oral squamous cell carcinoma cells with HDM2 E3 ligase inhibitor led to the enhancement of expression of integrin beta 8 protein. In addition, the enhancement of expression of HDM2 protein promoted cell motility of oral squamous cell carcinoma cells. These findings indicated that HDM2 might tightlyregulate the degradation of integrin beta 8 protein by ubiquitin-proteasome system, and participate in regulation of invasion and metastasis of oral cancer. Therefore, it is expected that molecular targeted therapy targeting HDM2 ubiquitin ligase has the potential to be the novel therapy for oral squamous cell carcinoma.

Report

(3 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Annual Research Report
  • Research Products

    (4 results)

All 2015 2014

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (3 results)

  • [Journal Article] Overexpression of integrin αv facilitates proliferation and invasion of oral squamous cell carcinoma cells via MEK/ERK signaling pathway that is activated by interaction of integrin αvβ8 with type Ⅰ collagen2014

    • Author(s)
      Hayashido Y, Kitano H, Sakaue T, Fujii T, Suematsu M, Sakurai S, Okamoto T
    • Journal Title

      Int J Oncol

      Volume: 45(5) Issue: 5 Pages: 1875-1882

    • DOI

      10.3892/ijo.2014.2642

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] 顎下部に髄外性病変を生じた多発性骨髄腫の1例2015

    • Author(s)
      坂上泰士,小泉浩一, 中瀬洋司, 小川郁子, 虎谷茂昭, 岡本哲治
    • Organizer
      第60回(公社)日本口腔外科学会総会・学術大会
    • Place of Presentation
      名古屋国際会議場
    • Year and Date
      2015-10-18
    • Related Report
      2015 Annual Research Report
  • [Presentation] 扁平上皮癌細胞におけるsequestosome 1を介した選択的オートファジーによるインテグリンαvの蛋白翻訳後修飾2015

    • Author(s)
      末松美玲, 林堂安貴, 坂上泰士, 藤井隆彦, 岡本哲治
    • Organizer
      第69回NPO法人日本口腔科学会学術集会
    • Place of Presentation
      大阪国際会議場
    • Year and Date
      2015-05-14
    • Related Report
      2015 Annual Research Report
  • [Presentation] 扁平上皮癌細胞におけるsequestosome 1を介した選択的オートファジーによるインテグリンαvの蛋白翻訳後修飾2014

    • Author(s)
      末松美玲, 林堂安貴, 坂上泰士, 藤井隆彦, 岡本哲治
    • Organizer
      第51回日本口腔組織培養学会学術大会・総会
    • Place of Presentation
      九州歯科大学講堂
    • Year and Date
      2014-11-15
    • Related Report
      2014 Annual Research Report

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Published: 2014-09-09   Modified: 2017-05-10  

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