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These findings not only confirm the immunogenicity of ferroptosis but also expand the list of ferroptotic DAMPs responsible for its immunogenicity by adding CRT and ATP to the previously identified danger molecule decorin 20 and various oxidized products, including oxygenated phosphatidylethanolamine 70

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Metabolic abnormalities in PE directly influence lipid metabolic pathways involved in ferroptosis (Kagan et al., 2017)

The transcription factor Forkhead box O3a (FOXO3a) also regulates multiple antioxidant genes and is reduced in COPD lungs as a result of phosphoinositide-3-kinase (PI3K) activation [18,50]