生物
基因敲除
细胞生物学
细胞内
调节器
活性氧
糖酵解
细胞凋亡
癌症研究
程序性细胞死亡
抑制器
基因
生物化学
新陈代谢
作者
Karim Bensaad,Atsushi Tsuruta,Mary Selak,María Nieves Calvo Vidal,Katsunori Nakano,Ramón Bartrons,Eyal Gottlieb,Karen H. Vousden
出处
期刊:Cell
[Elsevier]
日期:2006-07-01
卷期号:126 (1): 107-120
被引量:1840
标识
DOI:10.1016/j.cell.2006.05.036
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.
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