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©The Author(s) 2025.
World J Gastroenterol. Aug 28, 2025; 31(32): 108654
Published online Aug 28, 2025. doi: 10.3748/wjg.v31.i32.108654
Published online Aug 28, 2025. doi: 10.3748/wjg.v31.i32.108654
Figure 4 Melatonin + CCT020312 or BPTES enhances anticancer effects and reduces Panc-1 and AsPC-1 cell viability.
A: Panc-1 and AsPC-1 cells were treated with high melatonin concentrations combined with the protein kinase R-like endoplasmic reticulum kinase agonist CCT020312 for 24 hours, and cell viability was assessed using the cell counting kit-8 assay (n = 3); B: Colony formation assay showing the effect of combined treatment of melatonin and CCT020312; C: Panc-1 and AsPC-1 cells were treated with high melatonin concentrations combined with the glutaminase 1 inhibitor BPTES for 24 hours, and cell viability was assessed using the cell counting kit-8 assay (n = 3); D: Colony formation assay showing the effect of combined treatment of melatonin and BPTES. MLT: Melatonin; DMSO: Dimethyl sulfoxide. bP < 0.01, cP < 0.001, and dP < 0.0001.
- Citation: Zhao Q, Zhang H, Wu HM, Yang QY, Zhao H, Kang L, Lv XY. Melatonin-induced ferroptosis in pancreatic cancer cells by stimulating endoplasmic reticulum stress and inhibiting alanine-serine-cysteine transporter 2-driven glutamine metabolism. World J Gastroenterol 2025; 31(32): 108654
- URL: https://www.wjgnet.com/1007-9327/full/v31/i32/108654.htm
- DOI: https://dx.doi.org/10.3748/wjg.v31.i32.108654