拟肽
细胞凋亡
癌症
Bcl-2家族
小分子
功能(生物学)
癌症研究
药物发现
生物
蛋白质家族
程序性细胞死亡
生物信息学
计算生物学
细胞生物学
生物化学
遗传学
基因
肽
作者
Naval Bajwa,Chenzhong Liao,Zaneta Nikolovska‐Coleska
标识
DOI:10.1517/13543776.2012.644274
摘要
The feasibility of disrupting protein-protein interactions between anti-apoptotic and pro-apoptotic proteins, members of the Bcl-2 family, using peptidomimetics and small-molecule inhibitors has been successfully established. Three small-molecule inhibitors have entered human clinical trials, which will allow the evaluation of this potential therapeutic approach in cancer patients. It will be important to gain a better understanding of pan and selective Bcl-2 inhibitors in order to facilitate future drug design efforts.
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