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A 2012 study in the Journal of Peptide Science compared copper-bound and copper-free forms of the tripeptide in skin stem-cell-recovery models, providing a direct fragment-versus-complex contrast useful for interpreting the broader literature (PMID 23019153)
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Therefore, targeting FSP1 to inhibit its activity, thus promoting ferroptosis, may be a promising approach for cancer therapy, particularly in the case of difficult-to-treat tumors
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10.1016/j.carbpol.2023.120714 86 ZengY.WuY.ZhangQ.XiaoX
