Distinct responses of compartmentalized glutathione redox potentials to pharmacologic quinones targeting NQO1
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文摘
Pharmacologic quinones elicit distinct compartmentalized oxidation of glutathione poise. Cytosolic oxidation is NQO1-dependent whereas mitochondrial is cell line dependent. High DNQ potency is result of its outstanding NQO1 substrate specificity. Low DNQ concentrations required for solid cancer treatments mitigate off target effects. β-lapachone at pharmacologic doses triggers oxidation of cysteines in normal cells.

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