Analysis of the mechanism for control of proliferation of ovarian and endometrial cancer stem cells
Project/Area Number |
15K20132
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Obstetrics and gynecology
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Research Institution | Niigata University |
Principal Investigator |
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Project Period (FY) |
2015-04-01 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2017: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2016: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2015: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
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Keywords | がん幹細胞 / 子宮体がん / 卵巣がん / SOX2 |
Outline of Final Research Achievements |
We established and grew spheroid cell cultures from a variety of endometrial and ovarian cancer specimens. Endometrial cancer spheroid cells that expressed the cancer stem cell specific marker X formed larger tumors and grew more rapidly than the cells that did not express marker X. These results demonstrate the importance of marker X in proliferation of endometrial cancer stem cells. All procedures were performed following protocols approved by the Ethics and Animal Care and Use Committees of Niigata University.
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Report
(4 results)
Research Products
(5 results)
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[Journal Article] Sox2-dependent inhibition of p21 is associated with poor prognosis of endometrial cancer.2017
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
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Journal Title
Cancer Sci.
Volume: 108
Issue: 4
Pages: 632-640
DOI
Related Report
Peer Reviewed / Open Access
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