Effect of Exposure to Calcium Entry Blockers on Doxorubicin Accumulation and Cytotoxicity in Multidrug-Resistant Cells
- 7 March 1990
- journal article
- research article
- Published by Oxford University Press (OUP) in JNCI Journal of the National Cancer Institute
- Vol. 82 (5) , 419-424
- https://doi.org/10.1093/jnci/82.5.419
Abstract
Flow cytometry has been used to measure doxorubicin (DOX) retention in several pairs of drug-sensitive and multidrug-resistant (MDR) cell lines and in unselected human tumor cell lines. Coexposure to serveral agents that have been reported to reverse multidrug resistance, particularly calcium entry blockers (CEBs), produced a dose-dependent increase in DOX accumulation in MDR cell lines. In MDR Chinese hamster ovary cells (CH R C5), DOX levels declined rapidly following removel of CEBs, reaching a plateau value above that found in cells treated with DOX alone; this small increase probably represents DOX that is not accessible to the p170 efflux pump overexpressed in these cells. Increased DOX retention could be observed even after brief exposure to CEBs and washout and correlates with a decrease in cell proliferation over a 3-day growth assay. These results suggest that only a brief inhibition of drug efflux is sufficient to produce a meaningful reversal of drug resistance. [J Natl Cancer Inst 82: 419–424, 1990]This publication has 7 references indexed in Scilit:
- CLINICAL-TRIAL OF CONTINUOUS INFUSION VERAPAMIL, BOLUS VINBLASTINE, AND CONTINUOUS INFUSION VP-16 IN DRUG-RESISTANT PEDIATRIC TUMORS1989
- MOST DRUGS THAT REVERSE MULTIDRUG RESISTANCE ALSO INHIBIT PHOTOAFFINITY-LABELING OF P-GLYCOPROTEIN BY A VINBLASTINE ANALOG1988
- Patterns of anthracycline retention modulation in human tumor cellsCytometry, 1987
- Isolation of human mdr DNA sequences amplified in multidrug-resistant KB carcinoma cells.Proceedings of the National Academy of Sciences, 1986
- FLOW CYTOMETRIC MONITORING OF CELLULAR ANTHRACYCLINE ACCUMULATION IN MURINE LEUKEMIC-CELLS1986
- FLOW CYTOMETRIC STUDIES ON MODULATION OF CELLULAR ADRIAMYCIN RETENTION BY PHENOTHIAZINES1985
- REDUCED DRUG ACCUMULATION IN MULTIPLY DRUG-RESISTANT HUMAN-KB CARCINOMA CELL-LINES1985