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Novel therapeutic approach for endometriosis targeting variant isoforms of CD44

Research Project

Project/Area Number 18K09234
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 56040:Obstetrics and gynecology-related
Research InstitutionNara Medical University

Principal Investigator

OGAWA KENJI  奈良県立医科大学, 医学部附属病院, 研究員 (60623494)

Co-Investigator(Kenkyū-buntansha) 吉元 千陽  奈良県立医科大学, 医学部, 助教 (00526725)
棚瀬 康仁  奈良県立医科大学, 医学部, 助教 (20423915)
小林 浩  奈良県立医科大学, 医学部, 研究員 (40178330)
竹田 善紀  奈良県立医科大学, 医学部附属病院, 研究員 (50825239)
Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2020: ¥520,000 (Direct Cost: ¥400,000、Indirect Cost: ¥120,000)
Fiscal Year 2019: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2018: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords子宮内膜症 / CD44v9 / 酸化ストレス / ROS
Outline of Final Research Achievements

Endometriosis occurs in 7-10% of women of reproductive age and causes dysmenorrhea, infertility, and in rare cases, cancer. We focused on the oxidation-reduction reaction that occurs in endometriosis in order to develop a new treatment method. In the ELISA of tumor contents, we found that endometriosis was exposed to strong oxidative stress. Next, we examined the expression of CD44v9, oxidative and antioxidant markers (8OHdG, HO-1) by immunohistochemistry using pathological specimens operated at our hospital. We found that the antioxidant capacity was high in endometriosis and low in clear cell carcinoma, and that DNA damage increased as the antioxidant capacity decreased. It is thought that DNA damage increases as antioxidant capacity decreases.

Academic Significance and Societal Importance of the Research Achievements

子宮内膜症においては、嚢胞内で強い酸化ストレスに晒されている状態であるが、抗酸化作用を持つCD44v9の発現低下によって、酸化ストレスのマーカーである8-OHdGの発現が上昇していると推察された。抗酸化ストレス能の低下が、DNA損傷を増長させ、発癌リスクの上昇となる可能性が考えられ、今後CD44v9の発現低下の機序を明らかにしていくことで子宮内膜症の発生・癌化のメカニズムの解明や、治療法の開発へつながると考えられる。

Report

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

    (3 results)

All 2020 2018

All Presentation (3 results)

  • [Presentation] Immunohistochemical expression of CD44v9 and 8-OHdG in ovarian endometrioma and the benign endometriotic lesions adjacent to clear cell carcinoma.2020

    • Author(s)
      竹田善紀
    • Organizer
      第72回日本産科婦人科学会学術講演会
    • Related Report
      2020 Annual Research Report
  • [Presentation] 卵巣明細胞癌の発生、進展におけるCD44v9の関与2018

    • Author(s)
      小川憲二、山田有紀、小林浩
    • Organizer
      第27回日本がん転移学会
    • Related Report
      2018 Research-status Report
  • [Presentation] 子宮内膜症より発生した卵巣明細胞腺癌におけるCD44v9の免疫組織学的検討2018

    • Author(s)
      小川憲二、河原直紀、山田有紀、吉元千陽、川口龍二、佐道俊幸、小林浩
    • Organizer
      第40回日本エンドメトリオーシス学会
    • Related Report
      2018 Research-status Report

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

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