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Elucidation of chemoresistance of refracory cancer by single-cell gene expression analyses

Research Project

Project/Area Number 26293073
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypePartial Multi-year Fund
Section一般
Research Field Pathological medical chemistry
Research InstitutionNational Cancer Center Japan

Principal Investigator

Okamoto Koji  国立研究開発法人国立がん研究センター, その他部局等, その他 (80342913)

Co-Investigator(Renkei-kenkyūsha) NAKAGAMA Hitoshi  国立がん研究センター, 理事長 (30198030)
KATO Mamoru  国立がん研究センター研究所, 基盤的臨床開発研究コアセンター・バイオインフォマティクス部門, 部門長 (40391916)
Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥14,820,000 (Direct Cost: ¥11,400,000、Indirect Cost: ¥3,420,000)
Fiscal Year 2016: ¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2015: ¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2014: ¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Keywords癌 / 分子腫瘍学
Outline of Final Research Achievements

It is likely that cancer chemoresistance is attributed to a subset of chemoresistant cells in cancer tissues. Therefore, it will be important to understand cancer heterogeneity to overcome cancer chemorisitance and cure refractory cancer. We aimed to elucidate cancer heterogeneity by examining mouse xenograft tumors derived from in-vitro cultivated human colon cancer stem cells. By performing single-cell gene expression analyses of the tumors, we demonstrated that a subset of Lgr5-positive stem-like cells are associated with chemoresitance. We also performed single-cell analyses in a mouse model of colon carcinogenesis and identified a stem cell group that is responsible for tumorigenicity of colon tumors.

Report

(4 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Annual Research Report
  • 2014 Annual Research Report
  • Research Products

    (16 results)

All 2017 2016 2015 2014

All Journal Article (9 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 8 results,  Open Access: 7 results,  Acknowledgement Compliant: 2 results) Presentation (7 results) (of which Invited: 4 results)

  • [Journal Article] 卵巣がん幹細胞の鍵シグナル2017

    • Author(s)
      岡本康司
    • Journal Title

      月刊「細胞」

      Volume: 49 Pages: 108-111

    • Related Report
      2016 Annual Research Report
  • [Journal Article] Sox2-dependent inhibition of p21 is associated with poor prognosis of endometrial cancer2017

    • Author(s)
      Yamawaki K, Ishiguro T, Mori Y, Yoshihara K, Suda K, Tamura R, Yamaguchi M, Sekine M, Kashima K, Higuchi M, Fujii M, Okamoto K, Enomoto T
    • Journal Title

      Cancer Sci.

      Volume: 108 Issue: 4 Pages: 632

    • DOI

      10.1111/cas.13196

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Tumor-derived spheroids: class FormattedString { value: Relevance to cancer stem cells and clinical applications }2017

    • Author(s)
      Ishiguro T, Ohata H, Sato A, Yamawaki K, Enomoto T, Okamoto K.
    • Journal Title

      Cancer Sci.

      Volume: 108 Issue: 3 Pages: 283

    • DOI

      10.1111/cas.13155

    • URL

      https://localhost/en/publications/eef7fb2c-fd0d-4541-a89f-9f16a203d42e

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] TNIK inhibition abrogates colorectal cancer stemness2016

    • Author(s)
      Masuda M, Uno Y, Ohbayashi N, Ohata H, Mimata A, Kukimoto-Niino M, Moriyama H, Kashimoto S, Inoue T, Goto N, Okamoto K, Shirouzu M, Sawa M, Yamada T.
    • Journal Title

      Nature Comm.

      Volume: 7 Issue: 1 Pages: 12586-12586

    • DOI

      10.1038/ncomms12586

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Establishment and characterization of an in vitro model of ovarian cancer stem-like cells with an enhanced proliferative capacity2016

    • Author(s)
      Ishiguro T, Sato A, Ohata H, Ikarashi Y, Takahashi R, Ochiya T, Yoshida M, Tsuda H, Onda T, Kato T, Kasamatsu T, Enomoto T, Tanaka K, Nakagama H, Okamoto K.
    • Journal Title

      Cancer Research

      Volume: 76 Issue: 1 Pages: 150

    • DOI

      10.1158/0008-5472.can-15-0361

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Microrna library-based functional screening identified androgen-sensitive miR-216a as a player in bicalutamide resistance in prostate cancer2015

    • Author(s)
      Miyazaki T, Ikeda K, Horie-Inoue K, Okamoto K, Inoue S
    • Journal Title

      J. Clin. Med.

      Volume: 4 Issue: 10 Pages: 1853

    • DOI

      10.3390/jcm4101853

    • Related Report
      2015 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] MicroRNA-574-3p, identified by microRNA library-based functional screening, modulates tamoxifen response in breast cancer2015

    • Author(s)
      Ujihira T, Ikeda K, Suzuki T, Yamaga R, Sato W, Horie-Inoue K, Shigekawa T, Osaki A, Saeki T, Okamoto K, Takeda S, Inoue S
    • Journal Title

      Sci Rep

      Volume: 5 Issue: 1 Pages: 7641-7641

    • DOI

      10.1038/srep07641

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] MKK7 mediates miR-493-dependent suppression of liver metastasis of colon cancer cells2014

    • Author(s)
      Sakai H, Sato A, Aihara Y, Ikarashi Y, Midorikawa Y, Nakagama H, Okamoto K.
    • Journal Title

      Cancer Sci

      Volume: 105 Issue: 4 Pages: 425

    • DOI

      10.1111/cas.12380

    • URL

      https://pure.teikyo.jp/en/publications/77fa342c-3823-4c88-acd4-7e47ab6553c8

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Short hairpin RNA library-based functional screening identified ribosomal protein l31 that modulates prostate cancer cell growth via p53 pathway e1087432014

    • Author(s)
      Maruyama Y, Miyazaki T, Ikeda K, Okumura T, Sato W, Horie-Inoue K, Okamoto K, Takeda S, Inoue S
    • Journal Title

      PLoS ONE

      Volume: 9 Issue: 10 Pages: 828-833

    • DOI

      10.1371/journal.pone.0108743

    • URL

      https://pure.teikyo.jp/en/publications/5283fd41-a96f-4cca-af58-a45ca6a9c8d7

    • Related Report
      2014 Annual Research Report
    • Peer Reviewed / Open Access
  • [Presentation] スフェロイド形成による難治がん由来がん幹細胞の培養と特性解析2016

    • Author(s)
      岡本康司
    • Organizer
      第39 回日本分子生物学会年会
    • 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 Annual Research Report
    • Invited
  • [Presentation] 単一細胞レベルの遺伝子発現解析による大腸がんの造腫瘍性細胞及び治療抵抗性細胞の同定2015

    • Author(s)
      岡本康司
    • Organizer
      第38回日本分子生物学会年会
    • Place of Presentation
      神戸ポートアイランド
    • Year and Date
      2015-12-01
    • Related Report
      2015 Annual Research Report
    • Invited
  • [Presentation] 単一細胞レベルの遺伝子発現解析により示されたLgr5 陽性大腸がん幹細胞の多様性2015

    • Author(s)
      塩川大介、大畑広和、岡本康司
    • Organizer
      第74回日本癌学会年会
    • Place of Presentation
      横浜パシフィコ
    • Year and Date
      2015-10-08
    • Related Report
      2015 Annual Research Report
  • [Presentation] ヒト大腸がん幹細胞の転移能制御機構の解析2015

    • Author(s)
      岡本康司
    • Organizer
      第3回がんと代謝研究会
    • Place of Presentation
      石川県立音楽堂交流ホール
    • Year and Date
      2015-07-16
    • Related Report
      2015 Annual Research Report
    • Invited
  • [Presentation] 単一細胞レベルの発現解析による難治性固形がんの発がんメカニズムの解析2014

    • Author(s)
      岡本 康司
    • Organizer
      第37回日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2014-11-25 – 2014-11-27
    • Related Report
      2014 Annual Research Report
    • Invited
  • [Presentation] NADPH oxidaseの産生するROSはがん幹細胞の維持に広範な役割を果たす2014

    • Author(s)
      岡本 康司
    • Organizer
      第73回日本癌学会学術総会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2014-09-25 – 2014-09-27
    • Related Report
      2014 Annual Research Report
  • [Presentation] 肝転移巣由来の大腸がん幹細胞に特徴的な代謝プロファイルの検索2014

    • Author(s)
      岡本 康司
    • Organizer
      第22 回がん代謝研究会
    • Place of Presentation
      東京理科大学 葛飾キャンパス講堂
    • Year and Date
      2014-07-10 – 2014-07-11
    • Related Report
      2014 Annual Research Report

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Published: 2014-04-04   Modified: 2018-03-22  

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