©The Author(s) 2025.
World J Gastroenterol. Nov 7, 2025; 31(41): 111174
Published online Nov 7, 2025. doi: 10.3748/wjg.v31.i41.111174
Published online Nov 7, 2025. doi: 10.3748/wjg.v31.i41.111174
Figure 3 Effects of sorafenib, metformin and quiescin sulfhydryl oxidase 1 on ferroptosis.
Sorafenib enhances the ubiquitination of ferroptosis suppressor protein 1 through TRIM54, leading to the induction of ferroptosis by decreasing CoQH2. Furthermore, quiescin sulfhydryl oxidase 1 induces ferroptosis by inhibiting epidermal growth factor receptor, which subsequently inhibits nuclear factor erythroid 2-related factor 2. Metformin induces ferroptosis by inhibiting the P62/Kelch-like ECH-associated protein 1/nuclear factor erythroid 2-related factor 2/heme oxygenase 1 pathway. FSP1: Ferroptosis suppressor protein 1; Keap1: Kelch-like ECH-associated protein 1; Nrf2: Nuclear factor erythroid 2-related factor 2; EGFR: Epidermal growth factor receptor; HO-1: Heme oxygenase 1.
- Citation: Han JF, Jia ZY, Fan X, Zhao XY, Cheng LY, Xia YX, Ji XR, Zang WQ. Mechanisms of ferroptosis in primary hepatocellular carcinoma and progress of artificial intelligence-based predictive modeling in hepatocellular carcinoma. World J Gastroenterol 2025; 31(41): 111174
- URL: https://www.wjgnet.com/1007-9327/full/v31/i41/111174.htm
- DOI: https://dx.doi.org/10.3748/wjg.v31.i41.111174