期刊
MEDICINAL RESEARCH REVIEWS
卷 32, 期 6, 页码 1159-1196出版社
WILEY
DOI: 10.1002/med.20236
关键词
p53; MDM2; anticancer; structure-activity relationship (SAR)
资金
- National Natural Science Foundation of China [30873163]
- National Key Tech Project for Major Creation of New Drugs [2009ZX09501-003]
- Fundamental Research Funds for the Central Universities [KYJD038]
The powerful tumor suppressor p53 takes charge of a regulatory network to guard over the living cells from harmful effect of different forms of stress and eradicate the tumor cells for normal physiological condition maintenance. However the antitumor function of p53 is often attenuated or even omitted mainly due to two alternative mechanisms, direct gene alterations in p53 or negative controlled by MDM2 protein. In this article, overview on different therapeutic strategies that are exploited to restore the neoplasm therapeutic effect to p53 will be provided, including pharmacological rescue of mutant p53 and modulation of the p53-MDM2 interaction. We attempt to focus on the medicinal chemistry aspects of small molecule agents targeting the p53-MDM2 pathway and recent progress in these agents. In addition, the mechanism of action and anticancer activity of different classes of compounds targeting the p53-MDM2 pathway, as well as structureactivity relationships, are discussed.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据