Role of PML and the PML-nuclear body in the control of programmed cell death

被引:158
作者
Bernardi, R
Pandolfi, PP
机构
[1] Cornell Univ, Grad Sch Med Sci, Mem Sloan Kettering Canc Ctr, Sloan Kettering Div,Mol Biol Program, New York, NY 10021 USA
[2] Cornell Univ, Grad Sch Med Sci, Mem Sloan Kettering Canc Ctr, Sloan Kettering Div,Dept Pathol, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
apoptosis; PML-nuclear body; tumor suppression; transcription; transcription factors; cancer; APL;
D O I
10.1038/sj.onc.1207106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
PML is a tumor suppressor implicated in leukemia and cancer pathogenesis. PML epitomizes a multiprotein nuclear structure, the PML-nuclear body (PML-NB), whose proper formation and function depends on PML. Studies in knockout (KO) mic e and cells unraveled an essential pleiotropic role for PML in multiple p53-dependent and -independent apoptotic pathways. As a result, Pml(-/-) mice and cells are protected from apoptosis triggered by a number of stimuli such as ionizing radiation, interferon, ceramide, Fas and TNF. It is becoming apparent that PML and the PML-NB act as molecular hubs for the induction and/or reinforcement of programmed cell death through a selective and dynamic regulation of proapoptotic transcriptional events. In addition, recent observations propose a role for PML in checkpoint responses upon DNA damage. Moreover, PML and the PML-NB have also been implicated in the control of genomic stability and DNA repair. Here, we will discuss the molecular mechanisms by which PML regulates these processes and the implication of these findings for cancer pathogenesis and therapy.
引用
收藏
页码:9048 / 9057
页数:10
相关论文
共 70 条
[1]
Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome [J].
Bell, DW ;
Varley, JM ;
Szydlo, TE ;
Kang, DH ;
Wahrer, DCR ;
Shannon, KE ;
Lubratovich, M ;
Verselis, SJ ;
Isselbacher, KJ ;
Fraumeni, JF ;
Birch, JM ;
Li, FP ;
Garber, JE ;
Haber, DA .
SCIENCE, 1999, 286 (5449) :2528-2531
[2]
SUMO-1 protease-1 regulates gene transcription through PML [J].
Best, JL ;
Ganiatsas, S ;
Agarwal, S ;
Changou, A ;
Salomoni, P ;
Shirihai, O ;
Meluh, PB ;
Pandolfi, PP ;
Zon, LI .
MOLECULAR CELL, 2002, 10 (04) :843-855
[3]
Regulation and localization of the Bloom syndrome protein in response to DNA damage [J].
Bischof, O ;
Kim, SH ;
Irving, J ;
Beresten, S ;
Ellis, NA ;
Campisi, J .
JOURNAL OF CELL BIOLOGY, 2001, 153 (02) :367-380
[4]
A human Cds1-related kinase that functions downstream of ATM protein in the cellular response to DNA damage [J].
Brown, AL ;
Lee, CH ;
Schwarz, JK ;
Mitiku, N ;
Piwnica-Worms, H ;
Chung, JH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3745-3750
[5]
TELOMERE ELONGATION IN IMMORTAL HUMAN-CELLS WITHOUT DETECTABLE TELOMERASE ACTIVITY [J].
BRYAN, TM ;
ENGLEZOU, A ;
GUPTA, J ;
BACCHETTI, S ;
REDDEL, RR .
EMBO JOURNAL, 1995, 14 (17) :4240-4248
[6]
PML NBs associate with the hMre11 complex and p53 at sites of irradiation induced DNA damage [J].
Carbone, R ;
Pearson, M ;
Minucci, S ;
Pelicci, PG .
ONCOGENE, 2002, 21 (11) :1633-1640
[7]
THE PML GENE ENCODES A PHOSPHOPROTEIN ASSOCIATED WITH THE NUCLEAR MATRIX [J].
CHANG, KS ;
FAN, YH ;
ANDREEFF, M ;
LIU, JX ;
MU, ZM .
BLOOD, 1995, 85 (12) :3646-3653
[8]
Changou AC, 2001, BLOOD, V98, p99A
[9]
Chehab NH, 2000, GENE DEV, V14, P278
[10]
Homeodomain-interacting protein kinase-2 phosphorylates p53 at Ser 46 and mediates apoptosis [J].
D'Orazi, G ;
Cecchinelli, B ;
Bruno, T ;
Manni, I ;
Higashimoto, Y ;
Saito, S ;
Gostissa, M ;
Coen, S ;
Marchetti, A ;
Del Sal, G ;
Piaggio, G ;
Fanciulli, M ;
Appella, E ;
Soddu, S .
NATURE CELL BIOLOGY, 2002, 4 (01) :11-19