Paradoxical suppression of cellular senescence by p53

被引:242
作者
Demidenko, Zoya N. [1 ]
Korotchkina, Lioubov G. [1 ]
Gudkov, Andrei V. [1 ]
Blagosklonny, Mikhail V. [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA
基金
美国国家卫生研究院;
关键词
cell cycle; p21; rapamycin; mTOR; aging; TERMINAL PROLIFERATION ARREST; PROTEIN-SYNTHESIS; TUMOR-CELLS; PATHWAY; MDM2; ACTIVATION; GROWTH; CANCER; PHOSPHORYLATION; P21(WAF1/CIP1);
D O I
10.1073/pnas.1002298107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The tumor suppressor p53 is a canonical inducer of cellular senescence (irreversible loss of proliferative potential and senescent morphology). p53 can also cause reversible arrest without senescent morphology, which has usually been interpreted as failure of p53 to induce senescence. Here we demonstrate that p53-induced quiescence actually results from suppression of senescence by p53. In previous studies, suppression of senescence by p53 was masked by p53-induced cell cycle arrest. Here, we separated these two activities by inducing senescence through overexpression of p21 and then testing the effect of p53 on senescence. We found that in p21-arrested cells, p53 converted senescence into quiescence. Suppression of senescence by p53 required its transactivation function. Like rapamycin, which is known to suppress senescence, p53 inhibited the mTOR pathway. We suggest that, while inducing cell cycle arrest, p53 may simultaneously suppress the senescence program, thus causing quiescence and that suppression of senescence and induction of cell cycle arrest are distinct functions of p53. Thus, in spite of its ability to induce cell cycle arrest, p53 can act as a suppressor of cellular senescence.
引用
收藏
页码:9660 / 9664
页数:5
相关论文
共 39 条
[1]  
Blagosklonny MV, 1997, CANCER RES, V57, P320
[2]   Regulation of Protein Synthesis by Ionizing Radiation [J].
Braunstein, Steve ;
Badura, Michelle L. ;
Xi, Qiaoran ;
Formenti, Silvia C. ;
Schneider, Robert J. .
MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (21) :5645-5656
[3]   p21Waf1/Cip1/Sdi1 mediates retinoblastoma protein degradation [J].
Broude, E. V. ;
Swift, M. E. ;
Vivo, C. ;
Chang, B-D ;
Davis, B. M. ;
Kalurupalle, S. ;
Blagosklonny, M. V. ;
Roninson, I. B. .
ONCOGENE, 2007, 26 (48) :6954-6958
[4]   Awakening guardian angels: drugging the p53 pathway [J].
Brown, Christopher J. ;
Lain, Sonia ;
Verma, Chandra S. ;
Fersht, Alan R. ;
Lane, David P. .
NATURE REVIEWS CANCER, 2009, 9 (12) :862-873
[5]   p53 target genes Sestrin1 and Sestrin2 connect genotoxic stress and mTOR signaling [J].
Budanov, Andrei V. ;
Karin, Michael .
CELL, 2008, 134 (03) :451-460
[6]  
Chang BD, 1999, CANCER RES, V59, P3761
[7]   p21Waf1/Cip1/Sdi1-induced growth arrest is associated with depletion of mitosis-control proteins and leads to abnormal mitosis and endoreduplication in recovering cells [J].
Chang, BD ;
Broude, EV ;
Fang, J ;
Kalinichenko, TV ;
Abdryashitov, R ;
Poole, JC ;
Roninson, IB .
ONCOGENE, 2000, 19 (17) :2165-2170
[8]   Role of p53 and p21waf1/cip1 in senescence-like terminal proliferation arrest induced in human tumor cells by chemotherapeutic drugs [J].
Chang, BD ;
Xuan, YZ ;
Broude, EV ;
Zhu, HM ;
Schott, B ;
Fang, J ;
Roninson, IB .
ONCOGENE, 1999, 18 (34) :4808-4818
[9]   Regulation of the phosphorylation and integrity of protein synthesis initiation factor eIF4GI and the translational repressor 4E-BP1 by p53 [J].
Constantinou, C ;
Clemens, MJ .
ONCOGENE, 2005, 24 (30) :4839-4850
[10]   p53-induced inhibition of protein synthesis is independent of apoptosis [J].
Constantinou, C ;
Bushell, M ;
Jeffrey, IW ;
Tilleray, V ;
West, M ;
Frost, V ;
Hensold, J ;
Clemens, MJ .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (15) :3122-3132