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To further elucidate the therapeutic mechanisms underlying D-CuPs multivalent interactions, comprehensive proteomic analysis revealed two pivotal transcriptional regulators, the tumor suppressor protein p53 and histone deacetylase 7 (HDAC7) to be potential mechanistic targets

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and RMSP1, a synthetic peptide with strong penetration and anti-inflammatory activity, shows efficacy in atopic dermatitis models [13]