LIFE AND DEATH BY P53

被引:90
作者
ELLEDGE, RM
LEE, WH
机构
[1] UNIV TEXAS,HLTH SCI CTR,INST BIOTECHNOL,CTR MOLEC MED,SAN ANTONIO,TX 78245
[2] UNIV TEXAS,HLTH SCI CTR,DIV MED ONCOL,SAN ANTONIO,TX 78284
关键词
D O I
10.1002/bies.950171105
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
p53 is a multifunctional protein which plays a role in modulating gene transcription, policing cell cycle checkpoints, activating apoptosis, controlling DNA replication and repair, maintaining genomic stability and responding to genetic insults. Mutation of the p53 gene confers the single greatest known selective advantage favoring cancer formation. Point mutations result not only in the loss of tumor suppressor functions, but also in the gain of tumor promotion functions. These dual circumstances may be unique to p53 and, in part, could explain the relatively powerful force behind this selection pressure. General mechanisms of gain of function by mutated p53 may include alteration in transcriptional modulation and newly acquired targets for transcriptional regulation and protein binding, Despite the direct significance of p53 mutations, loss of the remaining wild-type allele is usually required for the formation of tumors in the natural setting. Novel applications of the basic scientific knowledge of p53 could lead to an improvement in cancer treatment, hopefully in the not so distant future.
引用
收藏
页码:923 / 930
页数:8
相关论文
共 93 条
[1]   SUPPRESSION OF HUMAN COLORECTAL-CARCINOMA CELL-GROWTH BY WILD-TYPE-P53 [J].
BAKER, SJ ;
MARKOWITZ, S ;
FEARON, ER ;
WILLSON, JKV ;
VOGELSTEIN, B .
SCIENCE, 1990, 249 (4971) :912-915
[2]   A PROTEOLYTIC FRAGMENT FROM THE CENTRAL REGION OF P53 HAS MARKED SEQUENCE-SPECIFIC DNA-BINDING ACTIVITY WHEN GENERATED FROM WILD-TYPE BUT NOT FROM ONCOGENIC MUTANT P53-PROTEIN [J].
BARGONETTI, J ;
MANFREDI, JJ ;
CHEN, XB ;
MARSHAK, DR ;
PRIVES, C .
GENES & DEVELOPMENT, 1993, 7 (12B) :2565-2574
[3]  
BRAITHWAITE AW, 1991, ONCOGENE, V6, P781
[4]   MOUSE P53 INHIBITS SV40 ORIGIN-DEPENDENT DNA-REPLICATION [J].
BRAITHWAITE, AW ;
STURZBECHER, HW ;
ADDISON, C ;
PALMER, C ;
RUDGE, K ;
JENKINS, JR .
NATURE, 1987, 329 (6138) :458-460
[5]   P53-DEPENDENT APOPTOSIS IN THE ABSENCE OF TRANSCRIPTIONAL ACTIVATION OF P53-TARGET GENES [J].
CAELLES, C ;
HELMBERG, A ;
KARIN, M .
NATURE, 1994, 370 (6486) :220-223
[6]  
CAJOT JF, 1992, CANCER RES, V52, P6956
[7]  
CASEY G, 1991, ONCOGENE, V6, P1791
[8]   GENETIC MECHANISMS OF TUMOR SUPPRESSION BY THE HUMAN P53 GENE [J].
CHEN, PL ;
CHEN, YM ;
BOOKSTEIN, R ;
LEE, WH .
SCIENCE, 1990, 250 (4987) :1576-1580
[9]   HOT-SPOT P53 MUTANTS INTERACT SPECIFICALLY WITH 2 CELLULAR PROTEINS DURING PROGRESSION OF THE CELL-CYCLE [J].
CHEN, YM ;
CHEN, PL ;
LEE, WH .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (10) :6764-6772
[10]  
CHEN YM, 1991, ONCOGENE, V6, P1799