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Regulation epithelial stem cells by reactive oxgens species during oncogenic transformation

Research Project

Project/Area Number 15K14390
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Tumor biology
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, 研究所, 分野長 (80342913)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords癌 / 幹細胞
Outline of Final Research Achievements

In general, reactive oxygen species (ROS) inhibit proliferation of non-tumor cells. Recently we found that high levels of ROS function to promote proliferation of colon cancer stem cells in vitro. We aimed to elucidate the molecular mechanism by which ROS differentially affect cell proliferation during carcinogenesis. In order to investigate the regulation of ROS levels during colon carcinogenesis, we established the in vitro three-dimensional culture from non-tumor and tumor tissues, and examined the gene expression profiles as well as ROS levels. We revealed that levels of NADPH oxidase increased during the carcinogenesis. Detailed investigation based on these observation is underway.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report
  • Research Products

    (10 results)

All 2017 2016 2015

All Journal Article (6 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 5 results,  Open Access: 4 results,  Acknowledgement Compliant: 1 results) Presentation (4 results) (of which Invited: 3 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 Research-status 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 Research-status 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 Research-status 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 Research-status 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 Research-status Report
    • Invited

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Published: 2015-04-16   Modified: 2018-03-22  

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