Classic and novel roles of p53:: prospects for anticancer therapy

被引:112
作者
Fuster, Jose J.
Sanz-Gonzalez, Silvia M.
Moll, Ute M.
Andres, Vicente [1 ]
机构
[1] CSIC, Vasc Biol Unit, IBV, Spanish Council Sci Res, Valencia 46010, Spain
[2] SUNY Stony Brook, Dept Pathol, Stony Brook, NY 11794 USA
关键词
D O I
10.1016/j.molmed.2007.03.002
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
The tumor suppressor p53 is a transcription factor that is frequently inactivated in human tumors. Therefore, restoring its function has been considered an attractive approach to restrain cancer. Typically, p53-dependent growth arrest, senescence and apoptosis of tumor cells have been attributed to transcriptional activity of nuclear p53. Notably, wild-type p53 gain-of-function enhances cancer resistance in the mouse, but it also accelerates aging in some models, possibly due to altered p53 activity. Therefore, the emerging evidence of mitochondrial transcription-independent activities of p53 has raised high expectations. Here, we review new developments in transcription-dependent and transcription-independent p53 functions, recent advances in targeting p53 for cancer treatment and the pitfalls of moving from the laboratory research to the clinical setting.
引用
收藏
页码:192 / 199
页数:8
相关论文
共 81 条
[1]   Transcriptional blockade induces p53-dependent apoptosis associated with translocation of p53 to mitochondria [J].
Arima, Y ;
Nitta, M ;
Kuninaka, S ;
Zhang, DW ;
Fujiwara, T ;
Taya, Y ;
Nakao, M ;
Saya, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (19) :19166-19176
[2]   MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY [J].
BARAK, Y ;
JUVEN, T ;
HAFFNER, R ;
OREN, M .
EMBO JOURNAL, 1993, 12 (02) :461-468
[3]   Post-translational modification of p53 in tumorigenesis [J].
Bode, AM ;
Dong, ZG .
NATURE REVIEWS CANCER, 2004, 4 (10) :793-805
[4]   p53 isoforms can regulate p53 transcriptional activity [J].
Bourdon, JC ;
Fernandes, K ;
Murray-Zmijewski, F ;
Liu, G ;
Diot, A ;
Xirodimas, DP ;
Saville, MK ;
Lane, DP .
GENES & DEVELOPMENT, 2005, 19 (18) :2122-2137
[5]   Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound [J].
Bykov, VJN ;
Issaeva, N ;
Shilov, A ;
Hultcrantz, M ;
Pugacheva, E ;
Chumakov, P ;
Bergman, J ;
Wiman, KG ;
Selivanova, G .
NATURE MEDICINE, 2002, 8 (03) :282-288
[6]   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
[7]   Cancer and ageing: Rival demons? [J].
Campisi, J .
NATURE REVIEWS CANCER, 2003, 3 (05) :339-349
[8]   ARF-BP1/mule is a critical mediator of the ARF tumor suppressor [J].
Chen, DL ;
Kon, N ;
Li, MY ;
Zhang, WZ ;
Qin, J ;
Gu, W .
CELL, 2005, 121 (07) :1071-1083
[9]   PUMA couples the nuclear and cytoplasmic proapoptotic function of p53 [J].
Chipuk, JE ;
Bouchier-Hayes, L ;
Kuwana, T ;
Newmeyer, DD ;
Green, DR .
SCIENCE, 2005, 309 (5741) :1732-1735
[10]   Pharmacologic activation of p53 elicits Bax-dependent apoptosis in the absence of transcription [J].
Chipuk, JE ;
Maurer, U ;
Green, DR ;
Schuler, M .
CANCER CELL, 2003, 4 (05) :371-381