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Elucidation of the mechanism of action of the olfactory receptor involved in cancer-specific metabolism

Research Project

Project/Area Number 18K07060
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 49030:Experimental pathology-related
Research InstitutionHokkaido University

Principal Investigator

Takei Norio  北海道大学, 医学研究院, 助教 (50523461)

Co-Investigator(Kenkyū-buntansha) 太田 明伸  愛知医科大学, 医学部, 講師 (30438048)
桜井 敬之  信州大学, 学術研究院医学系, 准教授 (80317825)
Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2020: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2018: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
KeywordsGPCR / ワールブルグ効果 / 癌 / 糖代謝 / CRISPR/Cas9 / 嗅受容体 / CRISPR./Cas9 / OR7C1 / Warburg effect / GCPR / olfactory receptor / cancer / warburg effect
Outline of Final Research Achievements

In glucose metabolism, cancer cells are known to have a predominant energy metabolism by glycolysis, even in an aerobic environment, as compared to normal cells. This property has been suggested to be associated with malignant tumors of cancer in various stress environments within the tumor.
In this study, we focused on the characteristic metabolic pathways of cancer that differ from these normal cells and conducted a study about the role of a orphan receptor, which is thought to be involved in its metabolism, and the verification of therapeutic effect of its inhibition. This result suggested that this molecule may be involved in the regulation of major metabolic enzymes in cancer-specific energy metabolic pathways, and expected to be a novel target molecule in cancer treatment.

Academic Significance and Societal Importance of the Research Achievements

申請者は、癌の特殊なエネルギー代謝として知られ、癌の悪性化に影響を及ぼす可能性が示されているワールブルグ効果に着目し、その機構への関連が示唆される分子の機能を解明し治療への応用が可能かの基礎的知見を示した。
癌細胞は正常の細胞とは異なり、高い増殖能と分化・転移能を有しており、生物学的に癌細胞においてそのような悪性化に影響をおよぼす因子は治療標的・診断マーカーとなる可能性があることから、それらに関与する新規の因子を同定し、その役割を明らかにすることは、新しい治療法や診断法の開発に有用である。

Report

(4 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (9 results)

All 2020 2019 2018

All Journal Article (3 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 3 results,  Open Access: 3 results) Presentation (6 results)

  • [Journal Article] Novel Interleukin-6 Inducible Gene PDZ-Binding Kinase Promotes Tumor Growth of Multiple Myeloma Cells2020

    • Author(s)
      Ota Akinobu、Hanamura Ichiro、Karnan Sivasundaram、Inaguma Shingo、Takei Norio、Lam Vu Quang、Mizuno Shohei、Kanasugi Jo、Wahiduzzaman Md、Rahman Md Lutfur、Hyodo Toshinori、Konishi Hiroyuki、Tsuzuki Shinobu、Ikeda Hiroshi、Takami Akiyoshi、Hosokawa Yoshitaka
    • Journal Title

      Journal of Interferon & Cytokine Research

      Volume: 40 Issue: 8 Pages: 389-405

    • DOI

      10.1089/jir.2020.0111

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] ERO1α is a novel endogenous marker of hypoxia in human cancer cell lines2019

    • Author(s)
      Takei Norio、Yoneda Akihiro、Kosaka Marina、Sakai-Sawada Kaori、Tamura Yasuaki
    • Journal Title

      BMC Cancer

      Volume: 19 Issue: 1 Pages: 510-510

    • DOI

      10.1186/s12885-019-5727-9

    • Related Report
      2019 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Bindel-PCR: a novel and convenient method for identifying CRISPR/Cas9-induced biallelic mutants through modified PCR using Thermus aquaticus DNA polymerase2019

    • Author(s)
      Sakurai Takayuki、Kamiyoshi Akiko、Takei Norio、Watanabe Satoshi、Sato Masahiro、Shindo Takayuki
    • Journal Title

      Scientific Reports

      Volume: 9 Issue: 1 Pages: 9923-9923

    • DOI

      10.1038/s41598-019-46357-8

    • Related Report
      2019 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] Deletion of Pbk Locus by using CRISPR/Cas9-based gene editing without apparent phenotype in C57BL/6 Mice2020

    • Author(s)
      武井則雄, 太田明伸, シバスンダランカルナン, 稲熊真悟, 細川好孝
    • Organizer
      日本動物学会第91回大会
    • Related Report
      2020 Annual Research Report
  • [Presentation] ERO1αは癌における新規内在性低酸素マーカーと成り得る2018

    • Author(s)
      武井 則雄, 米田 明弘, 澤田 香織, 小坂 まりな, 田村 保明
    • Organizer
      第77回 日本癌学会学術総会
    • Related Report
      2018 Research-status Report
  • [Presentation] 癌におけるERO1αの新規内在性低酸素マーカーとしての有効性の検証2018

    • Author(s)
      武井 則雄, 米田 明弘, 澤田 香織, 小坂 まりな, 田村 保明
    • Organizer
      第13回 臨床ストレス応答学会大会
    • Related Report
      2018 Research-status Report
  • [Presentation] HSP47はトリプルネガティブ乳癌の転移能を増強する2018

    • Author(s)
      米田 明弘, 武井 則雄, 澤田 香織, 小坂 まりな, 田村 保明
    • Organizer
      第77回 日本癌学会学術総会
    • Related Report
      2018 Research-status Report
  • [Presentation] トリプルネガティブ乳癌の転移能におけるHSP47の作用機序の解明2018

    • Author(s)
      米田 明弘, 武井 則雄, 澤田 香織, 小坂 まりな, 田村 保明
    • Organizer
      第13回 臨床ストレス応答学会大会
    • Related Report
      2018 Research-status Report
  • [Presentation] HSP47によるトリプルネガティブ乳癌の転移能獲得機序の解明2018

    • Author(s)
      米田 明弘, 武井 則雄, 澤田 香織, 小坂 まりな, 田村 保明
    • Organizer
      第41回日本分子生物学会年会
    • Related Report
      2018 Research-status Report

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Published: 2018-04-23   Modified: 2022-01-27  

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