Elucidation of biological functions of CD133, a marker for brain tumor-initiating cells, and its application
Project/Area Number |
24659659
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Single-year Grants |
Research Field |
Cerebral neurosurgery
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Research Institution | 愛知県がんセンター(研究所) |
Principal Investigator |
IZAWA Ichiro 愛知県がんセンター(研究所), 腫瘍医化学部, 室長 (20311441)
|
Project Period (FY) |
2012-04-01 – 2014-03-31
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
|
Keywords | 脳腫瘍 / がん幹細胞 / CD133 / 癌幹細胞 |
Research Abstract |
CD133 is utilized as a marker for tumor-initiating cells of glioma, but its physiological function is still not well understood. To dissect the function of CD133, we tried to identify CD133-binding proteins, using pull-down methods, immunoprecipitation assays, and yeast two-hybrid techniques. On the other hand, we found that in human embryonic carcinoma NTERA-2 cells, CD133 suppresses the expression of Epithelial Splicing Regulatory Protein 1 (ESRP1), an RNA splicing factor that regulates epithelial-mesenchymal transition (EMT).
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Report
(3 results)
Research Products
(12 results)
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[Journal Article] Defect of mitotic vimentin phosphorylation causes microophthalmia and cataract via aneuploidy and senescence in lens epithelial cells2013
Author(s)
Matsuyama, M., Tanaka, H., Inoko, A., Goto, H., Yonemura, S., Kobori, K., Hayashi, Y., Kondo, E., Itohara, S., Izawa, I. and Inagaki, M
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Journal Title
J. Biol. Chem
Volume: 288
Pages: 35626-35635
Related Report
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[Journal Article] PI 3-kinase-dependent phosphorylation of Plk1-Ser99 promotes association with 14-3-3γ and is required for metaphase-anaphase transition2013
Author(s)
Kasahara, K., Goto, H., Izawa, I., Kiyono, T., Watanabe, N., Elowe, S., Nigg, E.A. and Inagaki, M.
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Journal Title
Nat. Commun.
Volume: 4
Issue: 1
Pages: 1882-1882
DOI
Related Report
Peer Reviewed / Open Access
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