Awakening guardian angels: drugging the p53 pathway

被引:743
作者
Brown, Christopher J. [1 ]
Lain, Sonia [2 ]
Verma, Chandra S. [3 ]
Fersht, Alan R. [4 ]
Lane, David P. [1 ]
机构
[1] ASTAR, Lab P53, Singapore 138648, Singapore
[2] Karolinska Inst, SE-17177 Stockholm, Sweden
[3] ASTAR, Bioinformat Inst, Matrix 138671, Singapore
[4] MRC, Ctr Prot Engn, Cambridge CB2 0QH, England
关键词
WILD-TYPE P53; SMALL-MOLECULE INHIBITORS; PROTEIN-PROTEIN INTERACTION; UBIQUITIN LIGASE ACTIVITY; STRUCTURE-BASED DESIGN; BASE EXCISION-REPAIR; TUMOR-SUPPRESSOR P53; DNA-BINDING FUNCTION; C-TERMINAL PEPTIDE; HUMAN CANCER-CELLS;
D O I
10.1038/nrc2763
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Currently, around 11 million people are living with a tumour that contains an inactivating mutation of TP53 (the human gene that encodes p53) and another 11 million have tumours in which the p53 pathway is partially abrogated through the inactivation of other signalling or effector components. The p53 pathway is therefore a prime target for new cancer drug development, and several original approaches to drug discovery that could have wide applications to drug development are being used. In one approach, molecules that activate p53 by blocking protein-protein interactions with MDM2 are in early clinical development. Remarkable progress has also been made in the development of p53-binding molecules that can rescue the function of certain p53 mutants. Finally, cell-based assays are being used to discover compounds that exploit the p53 pathway by either seeking targets and compounds that show synthetic lethality with TP53 mutations or by looking for non-genotoxic activators of the p53 response.
引用
收藏
页码:862 / 873
页数:12
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