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Elucidation of Epigenetics in Head and Neck Squamous Cell Carcinoma.

Research Project

Project/Area Number 25293414
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypePartial Multi-year Fund
Section一般
Research Field Surgical dentistry
Research InstitutionKanagawa Dental College

Principal Investigator

Kubota Eiro  神奈川歯科大学, 歯学部, その他 (50170030)

Co-Investigator(Kenkyū-buntansha) KONDO TADANORI  神奈川歯科大学, 歯学部, その他 (00587727)
IKOMA TAKEHARU  神奈川歯科大学, 大学院歯学研究科, 助教 (10638290)
OZAWA SHIGEYUKI  神奈川歯科大学, 大学院歯学研究科, 講師 (40434394)
SUZUKI KENJI  神奈川歯科大学, 大学院歯学研究科, 講師 (80350536)
MAEHATA YOUJIRO  神奈川歯科大学, 大学院歯学研究科, 講師 (80410009)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥17,810,000 (Direct Cost: ¥13,700,000、Indirect Cost: ¥4,110,000)
Fiscal Year 2015: ¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2014: ¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2013: ¥10,270,000 (Direct Cost: ¥7,900,000、Indirect Cost: ¥2,370,000)
KeywordsCXCL14 / BRAK / 頭頚部癌 / メチル化 / 頭頸部癌 / メチル化異常 / セツキシマブ
Outline of Final Research Achievements

We employed the CXCL14-expressing HSC-3 cells and the CXCL14-nonexpressing YCU-H891 cells as representatives of the two groups and compared their responses to cetuximab and their CXCL14 expression under various conditions. The growth of xenografted tumours initiated by HSC-3 cells, which expressed CXCL14 in vivo and in vitro, was suppressed by the injection of cetuximab into tumour-bearing mice, however neither the expression of the chemokine nor the cetuximab-dependent suppression of xenogarfted tumour growth were observed for YCU-H891 cells.
The inhibition of ERK MAP kinase signaling increased the levels of CXCL14 mRNA in HSC-3 cells, but not in YCU-H891 cells. We also found that the CXCL14 promoter region in YCU-H891 cells was hypermethylated, and that demethylation of the promoter by treatment with 5-aza-2’-deoxycytidine restored CXCL14 mRNA expression and in vivo cetuximab-mediated tumour-growth suppression.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Annual Research Report
  • 2013 Annual Research Report
  • Research Products

    (3 results)

All 2014 2013

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (2 results)

  • [Journal Article] Fasudil, a Rho kinase inhibitor, suppresses tumor growth by inducing CXCL14/BRAK in head and neck squamous cell carcinoma2014

    • Author(s)
      Chihiro MIYAMOTO, Yojiro MAEHATA, Kazuhiko MOTOHASHI, Shigeyuki OZAWA, Takeharu IKOMA, Kouki HIDAKA, Satoko WADA-TAKAHASHI, Shun-Suke TAKAHASHI, Fumihiko YOSHINO, Ayaka YOSHIDA, Eiro KUBOTA, Ryu-Ichiro HATA, Masaichi-Chang-il LEE
    • Journal Title

      Biomedical Research

      Volume: 35 Pages: 381-388

    • NAID

      130004903867

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] CXCL14のメチル化異常に着目したセツキシマブの抗腫瘍効果判定のための基礎研究2014

    • Author(s)
      近藤忠稚、小澤重幸、生駒丈晴、鈴木健司、久保田英朗
    • Organizer
      日本口腔外科学会総会・学術大会
    • Place of Presentation
      千葉 (幕張メッセ)
    • Year and Date
      2014-10-17 – 2014-10-19
    • Related Report
      2014 Annual Research Report
  • [Presentation] セツキシマブによる抗腫瘍性ケモカインBRAKの発現上昇メカニズムの解明2013

    • Author(s)
      小澤重幸
    • Organizer
      日本口腔外科学会総会
    • Place of Presentation
      福岡
    • Related Report
      2013 Annual Research Report

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Published: 2013-05-21   Modified: 2019-07-29  

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