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Ferroptosis plays a novel role in nonalcoholic steatohepatitis pathogenesis

Fei Xiong, Qiao Zhou, Xiaobo Huang, Peng Cao, Yi Wang

2022Frontiers in Pharmacology13 citationsDOIOpen Access PDF

Abstract

Ferroptosis relies on iron, and ferroptotic cell death is triggered when the balance of the oxidation-reduction system is disrupted by excessive lipid peroxide accumulation. A close relationship between ferroptosis and nonalcoholic steatohepatitis (NASH) is formed by phospholipid peroxidation substrates, bioactive iron, and reactive oxygen species (ROS) neutralization systems. Recent studies into ferroptosis during NASH development might reveal NASH pathogenesis and drug targets. Our review summarizes NASH pathogenesis from the perspective of ferroptosis mechanisms. Further, we discuss the relationship between mitochondrial dysfunction, ferroptosis, and NASH. Finally, potential pharmacological therapies directed to ferroptosis in NASH are hypothesized.

Topics & Concepts

Nonalcoholic steatohepatitisPathogenesisGPX4Reactive oxygen speciesLipid peroxidationSteatohepatitisProgrammed cell deathChemistryCell biologyOxidative stressMedicineCancer researchBiologyBiochemistryImmunologyNonalcoholic fatty liver diseaseFatty liverDiseaseApoptosisPathologySuperoxide dismutaseGlutathione peroxidaseFerroptosis and cancer prognosisCancer, Lipids, and MetabolismRNA modifications and cancer
Ferroptosis plays a novel role in nonalcoholic steatohepatitis pathogenesis | Litcius