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Targeting Ferroptosis as a Promising Therapeutic Strategy for Ischemia-Reperfusion Injury.

YiHang PanXueke WangXiwang LiuLihua ShenQixing ChenQiang Shu
Published in: Antioxidants (Basel, Switzerland) (2022)
Ischemia-reperfusion (I/R) injury is a major challenge in perioperative medicine that contributes to pathological damage in various conditions, including ischemic stroke, myocardial infarction, acute lung injury, liver transplantation, acute kidney injury and hemorrhagic shock. I/R damage is often irreversible, and current treatments for I/R injury are limited. Ferroptosis, a type of regulated cell death characterized by the iron-dependent accumulation of lipid hydroperoxides, has been implicated in multiple diseases, including I/R injury. Emerging evidence suggests that ferroptosis can serve as a therapeutic target to alleviate I/R injury, and pharmacological strategies targeting ferroptosis have been developed in I/R models. Here, we systematically summarize recent advances in research on ferroptosis in I/R injury and provide a comprehensive analysis of ferroptosis-regulated genes investigated in the context of I/R, as well as the therapeutic applications of ferroptosis regulators, to provide insights into developing therapeutic strategies for this devastating disease.
Keyphrases
  • cell death
  • cell cycle arrest
  • acute kidney injury
  • ischemia reperfusion injury
  • cardiac surgery
  • cancer therapy
  • gene expression
  • atrial fibrillation
  • fatty acid
  • atomic force microscopy