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Recent studies with animal models provide evidence that pheomelanin pigment pathway is implicated in UV radiation-independent carcinogenic contributions to melanomagenesis by mechanisms of oxidative damage 6,7,8 Two non-exclusive hypotheses were proposed to define pheomelanins pro-oxidant activity: (i) the pigment promotes the formation of damaging ROS and (ii) the pigment depletes protective antioxidants (e.g., glutathione) 9,10

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Evidence for lifespan extension and delayed age-related biomarkers in insulin receptor substrate 1 null mice