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10.1016/j.fsi.2023.108962 14 ChenP.ZhuZ.GengH.CuiX.HanY.WangL.et al (2024)

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Imatinib-induced GPX4 proteasomal degradation Imatinib is a tyrosine kinase inhibitor designed to inhibit BCR-ABL activity in chronic myelogenous leukemia (CML) that revolutionized the treatment of this hematopoietic malignancy in the early 2000s [46]

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Upstream stimulatory factor 2 inhibits erastin-induced ferroptosis in pancreatic cancer through transcriptional regulation of pyruvate kinase M2

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Monocytes and macrophages are also influenced by GSH levels

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