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In addition, CXCL10 antibody treatment in the CM group reversed the MCA205 tumor-induced increase in nuclear p-FOXO3A in PMFs (Supplementary Fig

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At the molecular level, the mechanism has been structurally resolved by NMR spectroscopy (Nature Communications, 2025): FOXO4-DRI binds to the disordered p53 TAD2 domain and forms a transiently folded complex through both the FOXO4-derived peptide region and its cationic cell permeability element