Ferroptosis: A novel therapeutic target for diabetic cardiomyopathy

doi:10.4239/wjd.v16.i6.104665

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Jun 15, 2025 (publication date) through Jul 28, 2025

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World Journal of Diabetes

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1948-9358

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Diabetes. Jun 15, 2025; 16(6): 104665
Published online Jun 15, 2025. doi: 10.4239/wjd.v16.i6.104665

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Figure 1 The primary signaling pathways and key regulatory factors of ferroptosis. TF: Transferrin; TFR1: Transferrin receptor1; DMT1: Divalent 311 metal transporter 1; ACSL4: Acyl-CoA synthetase long-chain family member 4; LPCAT3: Lysophosphatidylcholine acyltransferase 3; LOX: Lipoxygenase; SLC3A2: Solute carrier family 3 member 2; SLC7A11: Solute carrier family 7 member 11; GCL: Glutamate cysteine ligase; GSS: Glutathione synthase; Cys: Cystine; Glu: Glutamate; Gly: Glycine; NADPH: Nicotinamide adenine dinucleotide phosphate; ROS: Reactive oxygen species; PUFA: Polyunsaturated fatty acid; PUFA-PL: Polyunsaturated fatty acid-phospholipid; GPX4: Glutathione peroxidase; GSH: Glutathione.

Citation: Li GZ, Liu JY, Zhou H. Ferroptosis: A novel therapeutic target for diabetic cardiomyopathy. World J Diabetes 2025; 16(6): 104665
URL: https://www.wjgnet.com/1948-9358/full/v16/i6/104665.htm
DOI: https://dx.doi.org/10.4239/wjd.v16.i6.104665