
In conclusion, recent work has highlighted the fact that NSCLCs have elevated levels of NQO1 activity and that such an increase represents an excellent target for therapeutic exploitation. The 5-year survival rate seen with lung cancer is dismal and there is a high number of cancer deaths associated with this disease each year. This renders the design of molecules that can be activated by NQO1 (such as MeDZQ or CB 10-200) an extremely important and urgent issue.
Lung Neoplasms, Carcinoma, Non-Small-Cell Lung, Drug Design, Mitomycin, NAD(P)H Dehydrogenase (Quinone), Quinones, Humans, Oxidation-Reduction, Substrate Specificity
Lung Neoplasms, Carcinoma, Non-Small-Cell Lung, Drug Design, Mitomycin, NAD(P)H Dehydrogenase (Quinone), Quinones, Humans, Oxidation-Reduction, Substrate Specificity
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