Abstract
By definition, bioreductive anticancer agents require metabolic reduction to generate toxic species. In the case of bioreductive alkylating agents, activation by reductase enzymes is reversed by molecular oxygen. In some cases bioreduction can lead to detoxification. Thus the specificity of bioreductive drugs will be dependent upon the relative activities of appropriate activating and deactivating reductases in tumour versus normal tissues, as well as the comparative oxygen levels. Considerably greater attention has been focused upon oxygen as a controlling factor. Our complementary approach has been to concentrate on the molecular enzymology of reductive bioactivation.
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Workman, P., Walton, M.I. (1990). Enzyme-Directed Bioreductive Drug Development. In: Adams, G.E., Breccia, A., Fielden, E.M., Wardman, P. (eds) Selective Activation of Drugs by Redox Processes. NATO ASI Series, vol 198. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3768-7_16
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DOI: https://doi.org/10.1007/978-1-4615-3768-7_16
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