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Analysis of TGF-beta/Smad signal pathway involved in metastasis of oral squamous cell carcinoma

Research Project

Project/Area Number 25861934
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Surgical dentistry
Research InstitutionOsaka University

Principal Investigator

ATSUKO YONEKAWA  大阪大学, 歯学研究科, 招へい教員 (70600914)

Project Period (FY) 2013-04-01 – 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 2014: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords口腔扁平上皮癌 / 頸部リンパ節転移 / TGF-β / 運動能 / EMT / TGF-beta / リンパ節転移
Outline of Final Research Achievements

We exaimned the effect of TGF-β on the highly lymph nodes metastatic oral squamous cell carcinoma cell line, LM8 and its parental cell, SAS-GFP. We found that TGF-β didn't mediate their morphological change, cell to cell contact and growth. But, TGF-β induced increase in their migration and invasiveness. Epithelial-mesenchymal transition was inclined to be induced through up regulation of N-cadherin and Vimentin and enlogation of actin fiber in TGF-β stimulated cells. Additionaly, the expression of Wnt5b was elevated, not Wnt5a. Over all, these results suggest that TGF-β could increase migration and invasion of highly lymph nodes metastatic oral squamous cell carcinoma cell through EMT, in which Wnt5b could be involved.

Report

(5 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (7 results)

All 2016 2015 2014 2013

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (6 results)

  • [Journal Article] Wnt5b promotes the cell motility essential for metastasis of oral squamous cell carcinoma through active Cdc42 and RhoA2014

    • Author(s)
      Takeshita A, et al.
    • Journal Title

      International Journal of Oncology

      Volume: 44 Issue: 1 Pages: 59-68

    • DOI

      10.3892/ijo.2013.2172

    • Related Report
      2013 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] Wnt5bを介する口腔扁平上皮癌細胞の上皮間葉転換ならびに癌幹細胞様形質の誘導2016

    • Author(s)
      岸本聡子, 森田祥弘, 竹下彰範, 仁木敦子, 多田晋也, 濵田正和, 岩井聡一
    • Organizer
      第61回(公社)日本口腔外科学会・学術大会
    • Place of Presentation
      幕張メッセ 千葉県千葉市
    • Year and Date
      2016-11-25
    • Related Report
      2016 Annual Research Report
  • [Presentation] Wnt5bによるヒト口腔扁平上皮癌細胞の上皮間葉転換ならびに癌幹細胞様形質の誘導2015

    • Author(s)
      岸本聡子, 岩井聡一, 森田祥弘, 竹下彰範, 仁木敦子, 多田晋也, 由良義明
    • 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(名古屋市)
    • Year and Date
      2015-10-16
    • Related Report
      2015 Research-status Report
  • [Presentation] FibronectinはFocal adhesion kinaseのリン酸化を介して腫瘍リンパ管新生を促進する2015

    • Author(s)
      森田祥弘, 岩上隆紀, 仁木敦子, 楠山友紀子, 岩井聡一, 大亦哲司, 森田展雄, 由良義明
    • 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(名古屋市)
    • Year and Date
      2015-10-16
    • Related Report
      2015 Research-status Report
  • [Presentation] ヒト口腔扁平上皮癌におけるWntと上皮間葉転換の関連についての検討2015

    • Author(s)
      岸本聡子, 岩井聡一, 森田祥弘, 竹下彰範, 仁木敦子, 多田晋也, 由良義明
    • 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(大阪市)
    • Year and Date
      2015-05-13
    • Related Report
      2015 Research-status Report
  • [Presentation] Wnt5bはCdc42とRhoAを介して口腔扁平上皮癌細胞の細胞運動能を亢進する.2013

    • Author(s)
      竹下彰範, 岩井聡一, 仁木-米川敦子, 森田祥弘, 濱田正和, 奥長秀介, 由良義明
    • Organizer
      第58回日本口腔外科学会総会・学術大会
    • Place of Presentation
      福岡
    • Related Report
      2013 Research-status Report
  • [Presentation] Wnt5bは口腔扁平上皮癌細胞の運動能を亢進する.2013

    • Author(s)
      竹下彰範, 岩井聡一, 仁木-米川敦子, 森田祥弘, 濱田正和, 岩上隆紀, 由良義明
    • Organizer
      日本口腔組織培養学会設立50周年記念学術大会・総会
    • Place of Presentation
      東京
    • Related Report
      2013 Research-status Report

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Published: 2014-07-25   Modified: 2019-07-29  

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