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Uncovering the molecular mechanisms of OR7C1 in cancer biology.

Research Project

Project/Area Number 16K20874
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Biological pharmacy
Experimental pathology
Research InstitutionHokkaido University

Principal Investigator

Takei Norio  北海道大学, 産学・地域協働推進機構, 特任助教 (50523461)

Project Period (FY) 2016-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2017: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2016: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
KeywordsGPCR / OR7C1 / CRISPR/Cas9 / 糖代謝 / 癌 / 嗅神経細胞 / cancer / 癌幹細胞
Outline of Final Research Achievements

OR7C1 is a G protein coupled receptor and expressed in cancer stem cell and suggested the possibility as a novel factor of poor prognosis. However, the function in cancer remain unclear. In this study, to uncover the importance of OR7C1 expression in cancer biology, we generated conventional OR7C1 knockout clones by using the CRISPR/Cas9 system. As a result, OR7C1 KO decreased tumorigenicity and metastasis in vivo and cell proliferation under specific medium conditions in vitro. In conclusion, our findings suggest that OR7C1 is predominantly activated under specific condition such as starvation and contributes to cancer progression. Collectively, OR7C1 could be used as both a diagnostic biomarker of cancer exacerbation and a therapeutic target.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • Research Products

    (10 results)

All 2017 2016

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 1 results) Presentation (7 results)

  • [Journal Article] Endoplasmic reticulum oxidase 1α is critical for collagen secretion from and membrane type 1-matrix metalloproteinase levels in hepatic stellate cells2017

    • Author(s)
      Fujii M, Yoneda A, Takei N, Sakai-Sawada K, Kosaka M, Minomi K, Yokoyama A, Tamura Y.
    • Journal Title

      Journal of Biological Chemistry

      Volume: 292 Issue: 38 Pages: 15649-15660

    • DOI

      10.1074/jbc.m117.783126

    • NAID

      120006522663

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Hypoxia-inducible ERO1α promotes cancer progression through modulation of integrin-β1 modification and signalling in HCT116 colorectal cancer cells.2017

    • Author(s)
      Takei N, Yoneda A, Sakai-Sawada K, Kosaka M, Minomi K, Tamura Y.
    • Journal Title

      Sci Rep.

      Volume: 7(1) Issue: 1 Pages: 9389-9389

    • DOI

      10.1038/s41598-017-09976-7

    • NAID

      120006352230

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Spatiotemporal Regulation of Hsp90-Ligand Complex Leads to Immune Activation.2016

    • Author(s)
      Tamura Y, Yoneda A, Takei N, Sawada K.
    • Journal Title

      Front Immunol.

      Volume: 7

    • DOI

      10.3389/fimmu.2016.00201

    • Related Report
      2016 Research-status Report
    • Peer Reviewed
  • [Presentation] Heat shock protein 47 maintain cancer cell survival through its inhibitory effect on ER stress sensor IRE1α activity2017

    • Author(s)
      Akihiro Yoneda, Norio Takei, Kori Sakai-Sawada, Marina Kosaka, Kenjiro Minomi, Yasuaki Tamura.
    • Organizer
      American Association for Cancer Research
    • Place of Presentation
      WASHINGTON, DC, USA
    • Year and Date
      2017-04-01
    • Related Report
      2016 Research-status Report
  • [Presentation] 癌細胞におけるHSP47のERストレスセンサーIRE1αの活性調節機構2017

    • Author(s)
      米田明弘、武井則雄、澤田香織、小坂まりな、味呑憲二郎、田村保明
    • Organizer
      2017年度生命科学会合同年次大会(ConBio2017)
    • Related Report
      2017 Annual Research Report
  • [Presentation] HSP47はERストレスセンサーIRE1αの活性抑制を介して癌細胞増殖を調節する2017

    • Author(s)
      米田明弘、武井則雄、澤田香織、小坂まりな、味呑憲二郎、田村保明
    • Organizer
      第76回日本癌学会学術総会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 低酸素誘導性ERO1αは大腸がん細胞株においてがん増殖に寄与する2017

    • Author(s)
      武井則雄、米田明弘、澤田香織、田村保明
    • Organizer
      第76回日本癌学会学術総会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 癌細胞における HSP47 の IRE1α活性調節機構2017

    • Author(s)
      米田明弘、武井則雄、澤田香織、小坂まりな、味呑憲二郎、田村保明
    • Organizer
      第12回臨床ストレス応答学会大会
    • Related Report
      2017 Annual Research Report
  • [Presentation] ERO1α は低酸素環境下において integrin-β1 の立体構造形成に関与し癌細胞増 殖に寄与する2017

    • Author(s)
      武井則雄、米田明弘、澤田香織、小坂まりな、味呑憲二郎、田村保明
    • Organizer
      第12回臨床ストレス応答学会大会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 肝星細胞における小胞体酸化還元酵素ERO1αの機能解析2016

    • Author(s)
      米田明弘、藤井瑞希、武井則雄、澤田香織、横山敦郎、田村保明
    • Organizer
      日本分子生物学会
    • Place of Presentation
      パシフィコ横浜(神奈川県横浜市)
    • Year and Date
      2016-11-30
    • Related Report
      2016 Research-status Report

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Published: 2016-04-21   Modified: 2019-03-29  

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