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Identification of endometriosis-stem cells for the development of novel molecular-target therapy

Research Project

Project/Area Number 26670718
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Obstetrics and gynecology
Research InstitutionShimane University

Principal Investigator

SATORU KYO  島根大学, 医学部, 教授 (50272969)

Project Period (FY) 2014-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,380,000 (Direct Cost: ¥2,600,000、Indirect Cost: ¥780,000)
Fiscal Year 2016: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Keywords子宮内膜症 / 幹細胞 / 癌化
Outline of Final Research Achievements

To identify the stem cell of endometriosis, we first isolated epithelial and stromal cells from ovarian endometriomas resected by operation. The hTERT, cyclinD1 and CDK4 cDNAs were transfected to these cells by lentiviral transfection, and immortalized cells were successfully isolated. Using these cells, FACS analysis was performed, in which the cells with various cell surface markers were analyzed for invasion and sphere formation capacities. We found that CD44-positive cells have increased invasive ability and obtain efficient sphere formation activity, and therefore contain stem-cell population.

Report

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

    (6 results)

All 2017 2016 2015 2014

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 2 results) Presentation (3 results) (of which Invited: 2 results)

  • [Journal Article] The diagnostic utility of PAX8 immunostaining of malignant peritoneal mesothelioma presented as serous ovarian carcinomas: A single center experience of two cases.2017

    • Author(s)
      Nakamura K, Nakayama K, Nagaoka R, Nishisako K, Ishikawa M, Katagiri H, Sato E, Amano C, Kyo S.
    • Journal Title

      Oncol Lett.

      Volume: 13 Issue: 1 Pages: 263-266

    • DOI

      10.3892/ol.2016.5444

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] KRAS/BRAF Analysis in Ovarian Low-Grade Serous Carcinoma Having Synchronous All Pathological Precursor Regions.2016

    • Author(s)
      Nakamura K, Nakayama K, Ishibashi T, Ishikawa N, Ishikawa M, Katagiri H, Minamoto T, Sato E, Sanuki K, Yamashita H, Iida K, Sultana R, Kyo S.
    • Journal Title

      Int J Mol Sci.

      Volume: 17 Issue: 5 Pages: 625-625

    • DOI

      10.3390/ijms17050625

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Current concepts and practical techniques of nerve-sparing laparoscopic radical hysterectomy.2016

    • Author(s)
      Kyo S, Kato T, Nakayama K.
    • Journal Title

      Eur J Obstet Gynecol Reprod Biol.

      Volume: 207 Pages: 80-88

    • DOI

      10.1016/j.ejogrb.2016.10.033

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed
  • [Presentation] 細胞の機能異常:癌化過程を整理する2016

    • Author(s)
      京哲
    • Organizer
      第58回日本婦人科腫瘍学会
    • Place of Presentation
      米子市
    • Year and Date
      2016-08-26
    • Related Report
      2016 Annual Research Report
  • [Presentation] 卵巣チョコレート嚢胞の癌化を考える2015

    • Author(s)
      京哲
    • Organizer
      第36回日本エンドメトリオージス学会
    • Place of Presentation
      東京
    • Year and Date
      2015-01-25
    • Related Report
      2014 Research-status Report
    • Invited
  • [Presentation] 卵巣チョコレート嚢胞癌化の分子機構の解析2014

    • Author(s)
      京哲
    • Organizer
      第一回新潟産婦人科シンポジウム
    • Place of Presentation
      新潟市
    • Year and Date
      2014-09-14
    • Related Report
      2014 Research-status Report
    • Invited

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

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