Will the Ubiquitin System Furnish as Many Drug Targets as Protein Kinases?

被引:229
作者
Cohen, Philip [1 ,2 ]
Tcherpakov, Marianna [3 ]
机构
[1] MRC Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland
[2] Scottish Inst Cell Signalling, Sir James Black Ctr, Dundee DD1 5EH, Scotland
[3] BCC Res, Wellesley, MA 02481 USA
基金
英国医学研究理事会;
关键词
SMALL-MOLECULE INHIBITOR; UNANCHORED POLYUBIQUITIN CHAINS; KAPPA-B ACTIVATION; DEUBIQUITINATING ENZYME; DNA-DAMAGE; LIGASE; PROTEASOME; MDM2; P53; IDENTIFICATION;
D O I
10.1016/j.cell.2010.11.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein phosphorylation and protein ubiquitination regulate most aspects of cell life, and defects in these control mechanisms cause cancer and many other diseases. In the past decade, protein kinases have become one of the most important classes of drug targets for the pharmaceutical industry. In contrast, drug discovery programs that target components of the ubiquitin system have lagged behind. In this Perspective, we discuss the reasons for the delay in this pipeline, the drugs targeting the ubiquitin system that have been developed, and new approaches that may popularize this area of drug discovery in the future.
引用
收藏
页码:686 / 693
页数:8
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