Publication | Closed Access
Effect of verapamil and other agents on the distribution of anthracyclines and on reversal of drug resistance.
95
Citations
17
References
1987
Year
Intracellular DistributionBiochemistryMedicineNatural SciencesOther AgentsResistant CellPharmacotherapyAntimicrobial ChemotherapyAnti-cancer AgentCellular BiochemistryAntibiotic ResistancePharmacologyCell BiologyHydrophobic/hydrophilic SolubilityAntimicrobial ResistanceDrug DiscoveryDrug Resistance
We studied the intracellular distribution of drugs within anthracycline-sensitive and -resistant cells by computer-assisted digitized video fluorescence microscopy. We found that the antitumor antibiotic, daunorubicin, distributes differently in anthracycline-sensitive and -resistant human leukemia cells (HL-60). Verapamil and other agents known to circumvent resistance in pleiotropic drug-resistant cell lines were able to change the pattern of distribution of daunorubicin in the anthracycline-resistant HL-60 cells back to the distribution found in anthracycline-sensitive HL-60 cells. To investigate the biochemical basis for this effect, we studied the distribution of daunorubicin and doxorubicin in a hydrophobic/hydrophilic (membrane/cytoplasmic) environment using the two-compartment cell-free system of Folch. Our results demonstrate that various unrelated drugs known to overcome resistance will also change the distribution of the anthracyclines in the hydrophobic/hydrophilic compartments. Our data allow the hypothesis that various unrelated agents known to circumvent resistance may act by altering the hydrophobic/hydrophilic solubility of anthracyclines in the resistant cell.
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