Copyright: ©Author(s) 2026.
World J Gastrointest Oncol. Sep 15, 2026; 18(9): 123002
Published online Sep 15, 2026. doi: 10.4251/wjgo.123002
Published online Sep 15, 2026. doi: 10.4251/wjgo.123002
Table 3 Biological roles
| Pathway/biomarker | Role in copper metabolism or cuproptosis |
| FDX1 | Reduces Cu2+ to Cu+ and promotes lipoylation-dependent aggregation of TCA-cycle proteins, especially DLAT[31-33,97,122] |
| DLAT/LIAS/LIPT1/DLD (lipoylation-related genes) | Core components of mitochondrial protein lipoylation and lipoylated TCA-cycle protein aggregation during cuproptosis[31,34,43,47] |
| SLC31A1/ATP7A/ATP7B (copper transporters) | Regulate copper uptake and efflux; ATP7A/ATP7B can also influence platinum-drug transport and chemoresistance[11,16,30,52-56] |
| AOC1 | Copper-containing amine oxidase involved in polyamine catabolism and ROS-related metabolic stress[123,124] |
| ITGB1 | Integrin-mediated regulator of cell adhesion, metabolism, migration, and cuproptosis-related phenotypes[125,126] |
| SERPINE1 | Regulates extracellular matrix remodeling, EMT, angiogenesis, apoptosis, and immune infiltration[127-130] |
- Citation: Fang YP, Liu SN, Liu FP, Gong JW, Zhang YF, Lu JH, Liu JW, Wang Q, Chen X. Cuproptosis in gastric cancer: Mechanisms and therapeutic opportunities. World J Gastrointest Oncol 2026; 18(9): 123002
- URL: https://www.wjgnet.com/1948-5204/full/v18/i9/123002.htm
- DOI: https://dx.doi.org/10.4251/wjgo.123002