自噬
FOXO3公司
生物
细胞生物学
细胞凋亡
转录因子
程序性细胞死亡
彪马
袋3
贝肯1
癌症研究
信号转导
基因
遗传学
蛋白激酶B
作者
Brent E. Fitzwalter,Andrew Thorburn
出处
期刊:Autophagy
[Informa]
日期:2018-07-21
卷期号:14 (8): 1467-1468
被引量:74
标识
DOI:10.1080/15548627.2018.1475819
摘要
The molecular machinery linking macroautophagy (autophagy hereafter) to apoptosis is still being elucidated. A recent study found that the transcription factor FOXO3/FOXO3A (forkhead box O3), which regulates autophagy, is itself regulated by basal autophagy to determine apoptosis sensitivity. Autophagy inhibition confers cell sensitivity to anti-cancer agents, and this effect is explained by the ability of FOXO3 to transactivate the pro-apoptotic gene BBC3/PUMA. Here, we discuss the possibility that FOXO3 acts as a cell surveillance mechanism to correct autophagy perturbations (i.e., autophagy inhibition), and confers apoptosis sensitization if this autophagy imbalance is not rectified.
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