TIGAR, a p53-inducible regulator of glycolysis and apoptosis

被引:1584
作者
Bensaad, Karim
Tsuruta, Atsushi
Selak, Mary A.
Calvo Vidal, M. Nieves
Nakano, Katsunori
Bartrons, Ramon
Gottlieb, Eyal
Vousden, Karen H.
机构
[1] Beatson Inst Canc Res, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Barcelona, IDIBELL, Dept Ciencies Fisiol 2, Unitat Bioquim & Biol Mol, Lhospitalet De Llobregat 08907, Spain
关键词
D O I
10.1016/j.cell.2006.05.036
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, p53 tumor-suppressor protein prevents cancer development through various mechanisms, including the induction of cell-cycle arrest, apoptosis, and the maintenance of genome stability. We have identified a p53-inducible gene named TIGAR (TP53-induced glycolysis and apoptosis regulator). TIGAR expression lowered fructose-2,6-bisphosphate levels in cells, resulting in an inhibition of glycolysis and an overall decrease in intracellular reactive oxygen species (ROS) levels. These functions of TIGAR correlated with an ability to protect cells from ROS-associated apoptosis, and consequently, knockdown of endogenous TIGAR expression sensitized cells to p53-induced death. Expression of TIGAR may therefore modulate the apoptotic response to p53, allowing survival in the face of mild or transient stress signals that may be reversed or repaired. The decrease of intracellular ROS levels in response to TIGAR may also play a role in the ability of p53 to protect from the accumulation of genomic damage.
引用
收藏
页码:107 / 120
页数:14
相关论文
共 43 条
[1]   EVOLUTION OF A BIFUNCTIONAL ENZYME - 6-PHOSPHOFRUCTO-2-KINASE FRUCTOSE-2,6-BISPHOSPHATASE [J].
BAZAN, JF ;
FLETTERICK, RJ ;
PILKIS, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :9642-9646
[2]   Cells overexpressing fructose-2,6-bisphosphatase showed enhanced pentose phosphate pathway flux and resistance to oxidative stress [J].
Boada, J ;
Roig, T ;
Perez, X ;
Gamez, A ;
Bartrons, R ;
Cascante, M ;
Bermúdez, J .
FEBS LETTERS, 2000, 480 (2-3) :261-264
[3]   Regeneration of peroxiredoxins by p53-regulated sestrins, homologs of bacterial AhpD [J].
Budanov, AV ;
Sablina, AA ;
Feinstein, E ;
Koonin, EV ;
Chumakov, PM .
SCIENCE, 2004, 304 (5670) :596-600
[4]   Activation of p53 by oxidative stress involves platelet-derived growth factor-β receptor-mediated ataxia telangiectasia mutated (ATM) kinase activation [J].
Chen, K ;
Albano, A ;
Ho, A ;
Keaney, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (41) :39527-39533
[5]   An inducible gene product for 6-phosphofructo-2-kinase with an AU-rich instability element: Role in tumor cell glycolysis and the Warburg effect [J].
Chesney, J ;
Mitchell, R ;
Benigni, F ;
Bacher, M ;
Spiegel, L ;
Al-Abed, Y ;
Han, JH ;
Metz, C ;
Bucala, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :3047-3052
[6]   RETRACTED: Glucose-6-phosphate dehydrogenase plays a crucial role in protection from redox-stress-induced apoptosis (Retracted article. See JAN, 2023) [J].
Fico, A ;
Paglialunga, F ;
Cigliano, L ;
Abrescia, P ;
Verde, P ;
Martini, G ;
Iaccarino, I ;
Filosa, S .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (08) :823-831
[7]   New approaches to understanding p53 gene tumor mutation spectra [J].
Hollstein, M ;
Hergenhahn, M ;
Yang, Q ;
Bartsch, H ;
Wang, ZQ ;
Hainaut, P .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1999, 431 (02) :199-209
[8]   Fetal hemoglobin induction by histone deacetylase inhibitors involves generation of reactive oxygen species [J].
Hsiao, CH ;
Li, W ;
Lou, TF ;
Baliga, BS ;
Pace, BS .
EXPERIMENTAL HEMATOLOGY, 2006, 34 (03) :264-273
[9]   DNA-damaging reagents induce apoptosis through reactive oxygen species-dependent Fas aggregation [J].
Huang, HL ;
Fang, LW ;
Lu, SP ;
Chou, CK ;
Luh, TY ;
Lai, MZ .
ONCOGENE, 2003, 22 (50) :8168-8177
[10]   Puma is an essential mediator of p53-dependent and -independent apoptotic pathways [J].
Jeffers, JR ;
Parganas, E ;
Lee, Y ;
Yang, CY ;
Wang, JL ;
Brennan, J ;
MacLean, KH ;
Han, JW ;
Chittenden, T ;
Ihle, JN ;
McKinnon, PJ ;
Cleveland, JL ;
Zambetti, GP .
CANCER CELL, 2003, 4 (04) :321-328