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Expression and function of CDCA5 in OSCC

Research Project

Project/Area Number 26861727
Research Category

Grant-in-Aid for Young Scientists (B)

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

Principal Investigator

Tokuzen Norihiko  愛媛大学, 医学部附属病院, その他 (10723843)

Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords口腔扁平上皮癌 / CDCA5 / 予後 / 治療標的分子 / 治療標的
Outline of Final Research Achievements

We identified cell division cycle associated 5 (CDCA5) as a cancer-related gene which was overexpressed in all the human OSCC cells tested by microarray analysis. In this study, we investigated the expression and function of CDCA5 in OSCC. First, we confirmed that CDCA5 was overexpressed in human OSCC cell lines and OSCC tissues. We then tested the effect of synthetic small interfering RNAs specific for CDCA5 on the growth and invasion of human OSCC cells. Knockdown of CDCA5 markedly inhibited the growth of OSCC cells in vitro and in vivo. We also examined the expression of CDCA5 protein in 80 cases of OSCC immunohistochemically and found a significant association between CDCA5 expression levels and overall survival. These results suggest that CDCA5 functions as a critical gene supporting OSCC progression and that targeting CDCA5 may be a useful therapeutic strategy for OSCC.

Report

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

    (6 results)

All 2016 2015 2014 Other

All Journal Article (1 results) (of which Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (4 results) (of which Int'l Joint Research: 1 results) Remarks (1 results)

  • [Journal Article] Therapeutic potential of targeting cell division cycle associated 5 for oral squamous cell carcinoma2016

    • Author(s)
      Tokuzen N, Nakashiro K, Tanaka H, Iwamoto K, Hamakawa H
    • Journal Title

      Oncotarget

      Volume: 7 Issue: 3 Pages: 2343-53

    • DOI

      10.18632/oncotarget.6148

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] CDCA5 is a novel therapeutic target molecule in oral squamous cell carcinoma2016

    • Author(s)
      Norihiko Tokuzen, Koh-ichi Nakashiro, Hiroshi Tanaka, Kazuki Iwamoto, Hitoshi Akiyama, Hiroyuki Hamakawa
    • Organizer
      AACR Annual Meeting 2016
    • Place of Presentation
      Ernest N. Morial Convention Center, New Orleans, USA
    • Year and Date
      2016-04-16
    • Related Report
      2015 Annual Research Report
    • Int'l Joint Research
  • [Presentation] CDCA5 is a potential therapeutic target for oral squamous cell carcinoma2015

    • Author(s)
      Norihiko Tokuzen, Koh-ichi Nakashiro, Hiroshi Tanaka, Kazuki Iwamoto, Hiroyuki Hamakawa
    • Organizer
      第74回日本癌学会学術総会
    • Place of Presentation
      名古屋国際会議場, 名古屋市, 愛知県
    • Year and Date
      2015-10-08
    • Related Report
      2015 Annual Research Report
  • [Presentation] 口腔扁平上皮癌における新規治療標的分子 CDCA5 の同定2015

    • Author(s)
      徳善紀彦、中城公一、岩本和樹、田中宏史、浜川裕之
    • Organizer
      第19回日本がん分子標的治療学会
    • Place of Presentation
      松山全日空ホテル, 松山市, 愛媛県
    • Year and Date
      2015-06-10
    • Related Report
      2015 Annual Research Report
  • [Presentation] 口腔扁平上皮癌におけるCell Division Cycle Associated 5 の発現機能解析2014

    • Author(s)
      徳善 紀彦
    • Organizer
      第51回日本口腔組織培養学会
    • Place of Presentation
      北九州
    • Year and Date
      2014-11-15
    • Related Report
      2014 Research-status Report
  • [Remarks] 愛媛大学大学院医学系研究科 口腔顎顔面外科学分野

    • Related Report
      2015 Annual Research Report

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Published: 2014-04-04   Modified: 2017-05-10  

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