Bertrand Robert L
Department of Chemistry, University of Manitoba, Winnipeg R3T 2N2, Canada.
Med Hypotheses. 2017 Apr;101:69-74. doi: 10.1016/j.mehy.2017.02.017. Epub 2017 Feb 28.
Ferroptosis is a recently discovered form of regulated necrosis that involves iron-dependent lipid peroxidation. How cells die once ferroptosis is triggered remains unclear. Ferroptosis is hypothesized to require three critical events: (1) accumulation of redox-active iron, (2) glutathione depletion, and (3) lipid peroxidation. It is proposed that these three events must unfold simultaneously because stopping any critical event also stops ferroptosis. These events are hypothesized to amplify in severity through positive feedback loops. The cause of death in ferroptosis is therefore the synergistic combination of antioxidant depletion, iron toxicity, and membrane denaturation. The relevance of these feedback loops for cancer and neurodegenerative therapies is discussed.
铁死亡是最近发现的一种受调控的坏死形式,涉及铁依赖性脂质过氧化。铁死亡触发后细胞如何死亡仍不清楚。据推测,铁死亡需要三个关键事件:(1)氧化还原活性铁的积累,(2)谷胱甘肽耗竭,以及(3)脂质过氧化。有人提出,这三个事件必须同时发生,因为停止任何一个关键事件也会停止铁死亡。据推测,这些事件会通过正反馈回路在严重程度上放大。因此,铁死亡中的死亡原因是抗氧化剂耗竭、铁毒性和膜变性的协同组合。本文讨论了这些反馈回路在癌症和神经退行性疾病治疗中的相关性。