New insights into p53 activation

被引:0
|
作者
Christopher L Brooks
Wei Gu
机构
[1] Stemline Therapeutics,and Department of Pathology
[2] Inc.,undefined
[3] Institute for Cancer Genetics,undefined
[4] College of Physicians & Surgeons,undefined
[5] Columbia University,undefined
来源
Cell Research | 2010年 / 20卷
关键词
Mdm2; antirepression; destabilization; ubiquitination; transcriptional activation and stability;
D O I
暂无
中图分类号
学科分类号
摘要
The tumor suppressor p53 is a multifunctional, highly regulated, and promoter-specific transcriptional factor that is uniquely sensitive to DNA damage and cellular stress signaling. The mechanisms by which p53 directs a damaged cell down either a cell growth arrest or an apoptotic pathway remain poorly understood. Evidence suggests that the in vivo functions of p53 seem to balance the cell-fate choice with the type and severity of damage that occurs. The concept of antirepression, or inhibition of factors that normally keep p53 at bay, may help explain the physiological mechanisms for p53 activation. These factors also provide novel chemotherapeutic targets for the reactivation of p53 in tumors harboring a wild-type copy of the gene.
引用
收藏
页码:614 / 621
页数:7
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