期刊
CELL REPORTS
卷 22, 期 3, 页码 569-575出版社
CELL PRESS
DOI: 10.1016/j.celrep.2017.12.077
关键词
-
类别
资金
- NSF GRFP fellowship
- NIH [R35 CA197591, 4R00CA166517, 1R01GM122923]
- Damon Runyon-Rachleff innovation award
- NATIONAL CANCER INSTITUTE [R35CA197591, T32CA009302, R00CA166517] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM122923] Funding Source: NIH RePORTER
How cancer cells respond to nutrient deprivation remains poorly understood. In certain cancer cells, deprivation of cystine induces a non-apoptotic, iron-dependent form of cell death termed ferroptosis. Recent evidence suggests that ferroptosis sensitivity may be modulated by the stress-responsive transcription factor and canonical tumor suppressor protein p53. Using CRISPR/Cas9 genome editing, small-molecule probes, and high-resolution, time-lapse imaging, we find that stabilization of wildtype p53 delays the onset of ferroptosis in response to cystine deprivation. This delay requires the p53 transcriptional target CDKN1A (encoding p21) and is associated with both slower depletion of intracellular glutathione and a reduced accumulation of toxic lipid-reactive oxygen species (ROS). Thus, the p53-p21 axis may help cancer cells cope with metabolic stress induced by cystine deprivation by delaying the onset of non-apoptotic cell death.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据