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c-RGDKYQ is a synthetic cyclic peptide designed for targeted melanoma therapy. It leverages the overexpression of tyrosinase in melanoma cells to trigger enzyme-mediated oxidation and self-assembly into nanostructures. These structures selectively disrupt actin cytoskeleton dynamics in melanoma cells, leading to impaired motility, adhesion, and proliferation, ultimately inducing apoptosis. The drug displays high tumor selectivity and minimal systemic toxicity in animal models and does not use external drug payloads or complex delivery systems, relying solely on the peptide's own pharmacodynamic properties[1].
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