Publication | Open Access
Elesclomol restores mitochondrial function in genetic models of copper deficiency
99
Citations
25
References
2018
Year
GeneticsMolecular BiologyMolecular GeneticsFatal Mitochondrial DiseaseChemical BiologyRedox BiologyOxidative StressMitochondrial Copper ContentBiochemistryPharmacologyMitochondrial FunctionNatural SciencesMetalloproteinBioactive MetalMitochondrial MedicineCopper DeliveryMetabolismMedicineDrug Discovery
Significance Inherited pathogenic mutations in genes required for copper delivery to cytochrome c oxidase (CcO) perturb mitochondrial energy metabolism and result in fatal mitochondrial disease. A prior attempt to treat human patients with these mutations by direct copper supplementation was not successful, possibly because of inefficient copper delivery to the mitochondria. We performed a targeted search to identify compounds that can efficiently transport copper across biological membranes and identified elesclomol (ES), an investigational anticancer drug, as the most efficient copper delivery agent. ES rescues CcO function in yeast, zebrafish, and mammalian models of copper deficiency by increasing cellular and mitochondrial copper content. Thus, our study offers a possibility of repurposing this anticancer drug for the treatment of disorders of copper metabolism.
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