Review
Copyright ©The Author(s) 2025.
World J Diabetes. Jun 15, 2025; 16(6): 104665
Published online Jun 15, 2025. doi: 10.4239/wjd.v16.i6.104665
Figure 1
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.
Figure 2
Figure 2 Pathophysiological mechanism of diabetic cardiomyopathy. AGEs: Advanced glycation end products; RAAS: Renin-angiotensin-aldosterone system; DCM: Diabetic cardiomyopathy.
Figure 3
Figure 3 The regulatory role of ferroptosis in diabetic cardiomyopathy. Nrf2: Nuclear factor erythroid 2-related factor 2; SLC40A1: Solute carrier family 40 member 1; NCOA4: Nuclear receptor coactivator 4; 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; ROS: Reactive oxygen species; PUFA: Polyunsaturated fatty acid; PUFA-PL: Polyunsaturated fatty acid-phospholipid; GPX4: Glutathione peroxidase; GSH: Glutathione; ARE: Antioxidant response elements.