Search of mutant p53-specific target of cancer cells
Project/Area Number |
24650642
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Single-year Grants |
Research Field |
Clinical oncology
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Research Institution | Tohoku University |
Principal Investigator |
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Co-Investigator(Renkei-kenkyūsha) |
KATO Shunsuke 東北大学, 加齢医学研究所, 准教授 (40312657)
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Research Collaborator |
IMAI Hiroo 東北大学, 大学院医学系研究科, 大学院生
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Project Period (FY) |
2012-04-01 – 2014-03-31
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Project Status |
Completed (Fiscal Year 2013)
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Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
|
Keywords | 変異p53 / 合成致死 |
Research Abstract |
This study aimed to find out a synthetic lethal/sickness gene for cancer cells expressing R175H mutant p53, a most frequent mutation in human cancer. A lentiviral shRNA library was transfected in SF126 cells expressing R175H mutant p53 and multiple candidate synthetic lethal/sickness genes against R175H mutant p53 were isolated. One of genes, ID1, truly introduced synthetic lethal/sickness in SF126 by a lentivirus-mediated knockdown by ID1 shRNA. In future, development of ID1 inhibitor might contribute a new era of anti-cancer drugs.
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Report
(3 results)
Research Products
(4 results)
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[Presentation] High throughput RNAi screening of synthetic lethal genes interacting with the common TP53 mutation R175H2012
Author(s)
Imai, H.,Kato, S.,Sakamoto, Y.,Takahashi, S.,Kakudo Y.,Shimodaira H.,Ishioka C.
Organizer
The 103rd Annual Meeting of American Association of Cancer Research
Place of Presentation
Chicago, IL, U.S.A.
Year and Date
2012-04-02
Related Report
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