Identification of the genes regulate Ras-mediated signalingby cDNA expression cloning method
Project/Area Number |
22501010
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Tumor biology
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Research Institution | Kyoto University |
Principal Investigator |
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Project Period (FY) |
2010 – 2012
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Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2010: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
Keywords | がん制御遺伝子 |
Research Abstract |
It is important to regulate Ras-mediated signaling since constitutively active mutations of Ras genes are frequently found in various kinds of tumor cells. In this project we are aiming to identify genes with transformation suppressor activity against DT cells harboring constitutively active Ras oncogene. After a series of cDNA expression cloning around 80 candidate genes were identified.
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Report
(4 results)
Research Products
(8 results)
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[Journal Article] The transformation suppressor gene Reck is required for postaxial patterning in mouse forelimbs2012
Author(s)
Yamamoto M, Matsuzaki T, Takahashi R, Adachi E, Maeda Y, Yamaguchi S, Kitayama H, Echizenya M, Morioka Y, Alexander DB, Yagi T, Itohara S, Nakamura T, Akiyama H, Noda M
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Journal Title
Biology Open
Volume: (in press)
Issue: 5
Pages: 458-466
DOI
Related Report
Peer Reviewed
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[Journal Article] A novel screen using the Reck tumor suppressor gene promoter detects both conventional and metastasis-suppressing anticancer drugs2010
Author(s)
Murai R, Yoshida Y, Muraguchi T, Nishimoto E, Morioka Y, Kitayama H, Kondoh S, Kawazoe Y, Hiraoka M, Uesugi M, Noda M
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Journal Title
Oncotarget
Volume: 1
Pages: 252-64
URL
Related Report
Peer Reviewed
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