©The Author(s) 2026.
World J Clin Oncol. Feb 24, 2026; 17(2): 114959
Published online Feb 24, 2026. doi: 10.5306/wjco.v17.i2.114959
Published online Feb 24, 2026. doi: 10.5306/wjco.v17.i2.114959
Figure 1 Schematic overview of lipid metabolism reprogramming and its therapeutic targeting in pancreatic cancer.
This figure summarizes the key concepts of the manuscript, illustrating the six interconnected components: The four hallmark alterations in lipid metabolism, their multifaceted roles in inducing tumor progression and immunosuppression, and the emerging strategies for targeted therapy. FAO: Fatty acid oxidation; FASN: Fatty acid synthase; ACC: Acetyl-CoA carboxylase; LDLR: Low-density lipoprotein receptor; HMGCR: 3-hydroxy-3-methylglutaryl-CoA reductase; PC: Pancreatic cancer; DL-C: Low-density lipoprotein cholesterol; MDSCs: Myeloid-derived suppressor cells; STAT3: Signal transducer and activator of transcription 3; NF-κB: Nuclear factor kappa B; EGCG: Epigallocatechin gallate; HMGCR:3-hydroxy-3-methylglutaryl-CoA reductase; PPIs: Proton pump inhibitors; SCD: Stearoyl-CoA desaturase.
- Citation: Zhang C, Wang H, Yang YH. Lipid metabolism in pancreatic cancer treatment. World J Clin Oncol 2026; 17(2): 114959
- URL: https://www.wjgnet.com/2218-4333/full/v17/i2/114959.htm
- DOI: https://dx.doi.org/10.5306/wjco.v17.i2.114959
