氧化应激
活性氧
磷酸戊糖途径
癌变
癌细胞
转录因子
抗氧化剂
癌症研究
细胞生物学
癌症
细胞生长
生物化学
化学
氧化磷酸化
生物
新陈代谢
糖酵解
基因
遗传学
作者
John D. Hayes,Albena T. Dinkova‐Kostova,Kenneth D. Tew
出处
期刊:Cancer Cell
[Elsevier]
日期:2020-07-09
卷期号:38 (2): 167-197
被引量:1624
标识
DOI:10.1016/j.ccell.2020.06.001
摘要
Contingent upon concentration, reactive oxygen species (ROS) influence cancer evolution in apparently contradictory ways, either initiating/stimulating tumorigenesis and supporting transformation/proliferation of cancer cells or causing cell death. To accommodate high ROS levels, tumor cells modify sulfur-based metabolism, NADPH generation, and the activity of antioxidant transcription factors. During initiation, genetic changes enable cell survival under high ROS levels by activating antioxidant transcription factors or increasing NADPH via the pentose phosphate pathway (PPP). During progression and metastasis, tumor cells adapt to oxidative stress by increasing NADPH in various ways, including activation of AMPK, the PPP, and reductive glutamine and folate metabolism.
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