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Anti-proliferative activity of Adenoviral vector expressing short hairpin RNA targeting G-Protein coupled receptor (GPR87) in urothelial carcinoma

Research Project

Project/Area Number 25462482
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Urology
Research InstitutionKagawa University

Principal Investigator

zhang xia  香川大学, 医学部, 助教 (30524061)

Co-Investigator(Kenkyū-buntansha) Sugimoto Mikio  香川大学, 医学部, 准教授 (10243768)
Kakehi Yoshiyuki  香川大学, 医学部, 教授 (20214273)
Liu Dage  香川大学, 医学部, 助教 (30314941)
Hayashita Yushi  香川大学, 医学部, 助教 (30615034)
Hirama Hiromi  香川大学, 医学部, 助教 (50552725)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
KeywordsGPR87 / shRNA / Adenovirus / Gene therapy / xenograft / proliferation / apoptosis / Gene herapy / p53 / p21
Outline of Final Research Achievements

GPR87 is a newly deorphanized member of the cell surface molecule G protein-coupled receptor family. GPR signaling was shown to play a role in promotion of cell growth and survival, metastasis, and drug resistance. To explore effective gene therapies for GPR87-expressing cancers including urothelial cancer, we constructed an adenoviral vector expressing short hairpin RNA targeting GPR87 (Ad-shGPR87). We found that Ad-shGPR87 effectively inhibited the proliferation of GPR87-expressing cell lines both in vitro and in vivo. With this effective tool, we then analyzed the intracellular pathways to uncover the mechanism by which GPR87 is able to regulate the proliferation and survival of human bladder cancer cells. Further, knockdown of GPR87 led to a p53-dependent signal transduction and caused apoptosis in the bladder cancer cells. Consequently, GPR87 appeared to be a promising target for gene therapy. These results of were adopted by domestic and international conferences.

Report

(3 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2013 Research-status Report
  • Research Products

    (3 results)

All 2015 2013

All Journal Article (1 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 1 results,  Open Access: 1 results) Presentation (2 results)

  • [Journal Article] G Protein-Coupled Receptor 87 (GPR87) Promotes Cell Proliferation in Human Bladder Cancer Cells2015

    • Author(s)
      Zhang, X.; Liu, D.; Hayashida, Y.; Okazoe, H.; Hashimoto, T.; Ueda, N.; Sugimoto, M.; Kakehi, Y.,
    • Journal Title

      Int J Mol Sci

      Volume: 16 Issue: 10 Pages: 24319-31

    • DOI

      10.3390/ijms161024319

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Presentation] Anti-tumor activity of enhydrin in human prostate cancer cell lines.2013

    • Author(s)
      Xia Zhang, Dage Liu, Takuma Kato, Mikio Sugimoto, Yoshiyuki Kakehi, Hirotoshi Tamura, Yurika Kitai
    • Organizer
      第72回日本癌学会学術総会
    • Place of Presentation
      東京都
    • Related Report
      2013 Research-status Report
  • [Presentation] Expression and Role of GPR87 In Urothelial Carcinoma of The Bladder.2013

    • Author(s)
      Kakehi Yoshiyuki
    • Organizer
      URS
    • Place of Presentation
      オーストラリア
    • Related Report
      2013 Research-status Report

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

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