Targeting ferroptosis in gastrointestinal tumors: Interplay of iron-dependent cell death and autophagy.
Ferroptosis is a regulated cell death mechanism distinct from apoptosis, autophagy, and necroptosis, marked by iron accumulation and lipid peroxidation.
APA
Safari MH, Rahimzadeh P, et al. (2025). Targeting ferroptosis in gastrointestinal tumors: Interplay of iron-dependent cell death and autophagy.. Molecular and cellular probes, 79, 102013. https://doi.org/10.1016/j.mcp.2025.102013
MLA
Safari MH, et al.. "Targeting ferroptosis in gastrointestinal tumors: Interplay of iron-dependent cell death and autophagy.." Molecular and cellular probes, vol. 79, 2025, pp. 102013.
PMID
39837469
Abstract
Ferroptosis is a regulated cell death mechanism distinct from apoptosis, autophagy, and necroptosis, marked by iron accumulation and lipid peroxidation. Since its identification in 2012, it has developed into a potential therapeutic target, especially concerning GI disorders like PC, HCC, GC, and CRC. This interest arises from the distinctive role of ferroptosis in the progression of diseases, presenting a new avenue for treatment where existing therapies fall short. Recent studies emphasize the promise of focusing on ferroptosis to fight GI cancers, showcasing its unique pathophysiological mechanisms compared to other types of cell death. By comprehending how ferroptosis aids in the onset and advancement of GI diseases, scientists aim to discover novel drug targets and treatment approaches. Investigating ferroptosis in gastrointestinal disorders reveals exciting possibilities for novel therapies, potentially revolutionizing cancer treatment and providing renewed hope for individuals affected by these tumors.
MeSH Terms
Ferroptosis; Humans; Gastrointestinal Neoplasms; Autophagy; Iron; Animals; Cell Death