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- W1973057627 abstract "Based on the weight of evidence accrued in the past eight years, there is little question that the nuclear enzyme, topoisomerase II, serves as a common intracellular target for the cytotoxic effect of drugs of widely varying structure. The enzyme appears to be unique as a chemotherapy target in that it is recruited into a lethal process under the influence of drug. Its role contrasts sharply with other more classical chemotherapy targets, such as dihydrofolate reductase, whose activity must be successfully inhibited for the expression of cytotoxicity. Resistance to inhibitors of this enzyme frequently results from marked elevations in intracellular enzyme content. In contrast, the presence of topoisomerase is required for drug effect, and, in general, the greater the cellular content of the enzyme, the more sensitive the cell will be to these agents. However, important issues remain unresolved. The biochemical events that are initiated by cleavable complex formation and result in cell death must be more fully defined. It is likely a better understanding of the drug-enzyme interaction will be required for rational drug development. Finally, those aspects of the drug-topoisomerase interaction that confer therapeutic selectivity and/or clinical resistance are of paramount importance if the phenomenon is ever to be fully exploited." @default.
- W1973057627 created "2016-06-24" @default.
- W1973057627 creator A5054573802 @default.
- W1973057627 creator A5073466449 @default.
- W1973057627 date "1987-01-01" @default.
- W1973057627 modified "2023-09-26" @default.
- W1973057627 title "DNA topoisomerase II: A primer on the enzyme and its unique role as a multidrug target in cancer chemotherapy" @default.
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- W1973057627 doi "https://doi.org/10.1016/0163-7258(87)90054-4" @default.
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- W1973057627 hasPublicationYear "1987" @default.
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