Cyclosporin A reverses vincristine and daunorubicin resistance in acute lymphatic leukemia in vitro.
Lewis M. Slater, Paula M. Sweet, Marie Stupecky, Sudhir Gupta
Abstract
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Lewis M. Slater, Paula M. Sweet, Marie Stupecky, Sudhir Gupta
Abstract
Open-access reader
The development of drug resistance by tumor cells is a major obstacle to the cure of human malignancy. Cyclosporin A (CsA) completely reverses primary resistance to vincristine and cross resistance to daunorubicin in a pleiotropic drug-resistant subline of human T cell acute lymphatic leukemia. This subline is over 50-fold resistant to vincristine and fivefold resistant to daunorubicin. CsA has little effect on vincristine or daunorubicin activity in drug-sensitive parental leukemia and corrects daunorubicin resistance without altering cellular daunorubicin accumulation.
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The development of drug resistance by tumor cells is a major obstacle to the cure of human malignancy. Cyclosporin A (CsA) completely reverses primary resistance to vincristine and cross resistance to daunorubicin in a pleiotropic drug-resistant subline of human T cell acute lymphatic leukemia. This subline is over 50-fold resistant to vincristine and fivefold resistant to daunorubicin. CsA has little effect on vincristine or daunorubicin activity in drug-sensitive parental leukemia and corrects daunorubicin resistance without altering cellular daunorubicin accumulation.
Key concepts: Daunorubicin, Vincristine, Leukemia, Pharmacology, Drug resistance, Medicine, Cancer research, Immunology