Project/Area Number |
24650642
|
Research Category |
Grant-in-Aid for Challenging Exploratory Research
|
Allocation Type | Single-year Grants |
Research Field |
Clinical oncology
|
Research Institution | Tohoku University |
Principal Investigator |
|
Co-Investigator(Renkei-kenkyūsha) |
KATO Shunsuke 東北大学, 加齢医学研究所, 准教授 (40312657)
|
Research Collaborator |
IMAI Hiroo 東北大学, 大学院医学系研究科, 大学院生
|
Project Period (FY) |
2012-04-01 – 2014-03-31
|
Project Status |
Completed (Fiscal Year 2013)
|
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.
|