ReviewApoptosis : an international journal on programmed cell death2026
S-palmitoylation in ferroptosis: molecular mechanisms, modulators, and interplay with autophagy.
Review in Apoptosis : an international journal on programmed cell death, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
S-palmitoylation, a reversible lipid post-translational modification, plays a dynamically regulatory role in cell death signaling pathways by modulating protein-membrane affinity, subcellular localization, and functional interactions. Emerging evidence has linked dysregulated S-palmitoylation to various pathologies including cancer and neurodegenerative disorders. Recently, several advances highlight its novel involvement in ferroptosis, an iron-dependent programmed cell death mechanism characterized with lipid peroxidation and iron accumulation. However, the precise regulatory impact of S-palmitoylation on ferroptosis remains to be fully elucidated. Notably, certain key regulators of ferroptosis undergo degradation through autophagy pathways, indicating an intricate crosstalk between ferroptosis and autophagy. Herein, the current review summarized the molecular mechanisms and physiological functions of ferroptosis and S-palmitoylation, with a particular focus on the pivotal role of palmitoylated ferroptosis-related regulators. Importantly, the interaction between autophagy and ferroptosis, especially the S-palmitoylated proteins that modulate both processes were discussed as well. This review provides a new perspective for the accurate regulation of ferroptosis by modulating S-palmitoylation, thus may improve the overall prognosis through optimizing the treatment regimens or via enhancing the efficacy of existing therapies.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.