analysis of a new endogenous protein in endometrial cancer
Project/Area Number |
26830084
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Tumor biology
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Research Institution | Osaka Medical College |
Principal Investigator |
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Project Period (FY) |
2014-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
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Keywords | 子宮内膜細胞 / デコリン / プロゲステロン / ディナゲスト / 細胞周期 / 細胞外基質蛋白 / Decorin / EMT / 子宮内膜症 / 子宮内膜癌 / 上皮間葉転換 |
Outline of Final Research Achievements |
Decorin has been shown to be a powerful endogenous tumor repressor acting in a paracrine fashion to limit tumor growth. It was noted that progesterone and dienogest directly induced the binding of the decorin promoter.Progesterone and dienogest also led to significant induced cell cycle arrest via decorin by promoting production of p21. Decorin induced by dienogest appears to play a crucial role in suppressing endometriosis by exerting anti-proliferative effects and inducing cell cycle arrest via the production of p21 human ectopic endometrial cells and eutopic endometrial stromal cells.
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Report
(3 results)
Research Products
(3 results)
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[Journal Article] The EMT (epithelial-mesenchymal-transition)-related protein expression indicates the metastatic status and prognosis in patients with ovarian cancer.2014
Author(s)
Takai M, Terai Y, Kawaguchi H, Ashihara K, Fujiwara S, Tanaka T, Tsunetoh S, Tanaka Y, Sasaki H, Kanemura M, Tanabe A, Ohmichi M.
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Journal Title
J Ovarian Res.
Volume: 27
Pages: 76-80
Related Report
Peer Reviewed
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