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Single-cell gene expression analysis reveals the cellular heterogeneity of colon tumors and identifies novel therapeutic target genes

Research Project

Project/Area Number 18K07283
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 50020:Tumor diagnostics and therapeutics-related
Research InstitutionNational Cancer Center Japan

Principal Investigator

Shiokawa Daisuke  国立研究開発法人国立がん研究センター, 研究所, ユニット長 (90277278)

Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2020: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2019: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2018: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywordsシングルセル / がん幹細胞 / 大腸がん / 遺伝子発現解析 / Wntシグナル / 細胞多様性 / 細胞不均一性
Outline of Final Research Achievements

LGR5 is an established stem cell marker gene in many digestive tissues, and we previously showed that a subpopulation of LGR5+ cells in colon tumors were responsible for tumorigenicity. In this study, we demonstrated that the tumorigenic subpopulation of mouse LGR5+ cells exist in a quiescent state, and identified a unique gene signature that characterize these quiescent CSCs. Furthermore, seven of the signature genes are specifically expressed in a quiescent LGR5+ cells from xenografted human colon tumors and upregulated in colon cancer clinical specimens. Among these seven, PROX1 is expressed in invasive fronts of colon tumors, and shown to be induced by TCF7 to maintain a quiescent state. Importantly, PROX1 knockout significantly reduces tumor recurrence after chemotherapeutic treatment. The identified slow-cycling CSC signatures will be instrumental in targeting the chemoresistant CSCs and devising effective chemotherapy.

Academic Significance and Societal Importance of the Research Achievements

本研究の成果により、これまで不明であったLGR5陽性幹細胞群の細胞多様性が明らかなり、当該細胞集団が増殖型と休止型の2種に大別されることが示された。さらに休止型がん幹細胞で特異的に発現する遺伝子であるPROX1の機能を抑制することにより抗癌剤への感受性を高めることに成功した。即ち、本件研究の成果として得られた知見は、がん本態解明を目指す基礎研究としてのみならず、効果的ながん治療法の開発の礎となり社会に貢献する大きな意義を持つ研究成果であると考えられる。

Report

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

    (5 results)

All 2020 2019 2018

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

  • [Journal Article] Slow-cycling cancer stem cells regulate progression and chemoresistance in colon cancer2020

    • Author(s)
      Shiokawa Daisuke、Sakai Hiroaki、Ohata Hirokazu、Miyazaki Toshiaki、Kanda Yusuke、Sekine Shigeki、Narushima Daichi、Hosokawa Masahito、Kato Mamoru、Suzuki Yutaka、Takeyama Haruko、Kambara Hideki、Nakagama Hitoshi、Okamoto Koji
    • Journal Title

      Cancer Research

      Volume: 80 Issue: 20 Pages: 4451

    • DOI

      10.1158/0008-5472.can-20-0378

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed
  • [Journal Article] NOX1-Dependent mTORC1 Activation via S100A9 Oxidation in Cancer Stem-like Cells Leads to Colon Cancer Progression2019

    • Author(s)
      Ohata H, Shiokawa D, Obata Y, Sato A, Sakai H, Fukami M, Hara W, Taniguchi H, Ono M, Nakagama H, Okamoto K.
    • Journal Title

      Cell Rep.

      Volume: 28 Issue: 5 Pages: 1282

    • DOI

      10.1016/j.celrep.2019.06.085

    • Related Report
      2019 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] Transcriptional factor Tcf1 controls the drug resistance of Lgr5-positive colon tumor stem cells2019

    • Author(s)
      Daisuke Shiokawa, Hirokazu Ohata, Koji Okamoto
    • Organizer
      日本癌学会
    • Related Report
      2019 Research-status Report
  • [Presentation] The slow-growing sub-population of Lgr5-positive colon tumor stem cells is resistant to an anti-cancer drug treatment2018

    • Author(s)
      Daisuke Shiokawa
    • Organizer
      日本癌学会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Book] 阻害剤・活性化剤ハンドブック (秋山徹、河府和義 編)2019

    • Author(s)
      塩川大介
    • Total Pages
      646
    • Publisher
      羊土社
    • ISBN
      9784758120999
    • Related Report
      2019 Research-status Report

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

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