Program in Biomedical Sciences, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
College of Medicine, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Int J Mol Sci. 2021 Nov 22;22(22):12603. doi: 10.3390/ijms222212603.
Radiotherapy promotes tumor cell death and senescence through the induction of oxidative damage. Recent work has highlighted the importance of lipid peroxidation for radiotherapy efficacy. Excessive lipid peroxidation can promote ferroptosis, a regulated form of cell death. In this review, we address the evidence supporting a role of ferroptosis in response to radiotherapy and discuss the molecular regulators that underlie this interaction. Finally, we postulate on the clinical implications for the intersection of ferroptosis and radiotherapy.
放疗通过诱导氧化损伤促进肿瘤细胞死亡和衰老。最近的研究强调了脂质过氧化对于放疗效果的重要性。过量的脂质过氧化会促进铁死亡,这是一种受调控的细胞死亡形式。在这篇综述中,我们讨论了支持铁死亡在放疗反应中起作用的证据,并讨论了这种相互作用的分子调节剂。最后,我们推测了铁死亡和放疗交叉的临床意义。