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[Cancer Research 52, 3157-3163, June 1, 1992]
© 1992 American Association for Cancer Research

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Drug Transport Mechanisms in HL60 Cells Isolated for Resistance to Adriamycin: Evidence for Nuclear Drug Accumulation and Redistribution in Resistant Cells1

David Marquardt and Melvin S. Center2

Division of Biology, Kansas State University, Manhattan, Kansas 66506-4901

HL60 cells isolated for resistance to Adriamycin are multidrug resistant and defective in the cellular accumulation of drug. These cells do not contain detectable levels of P-glycoprotein. At the present time the mechanism by which HL60/Adr cells reduce drug levels is not known. To gain insight into the molecular basis of this system we have analyzed transport pathways and the distribution of daunomycin in drug-resistant HL60 cells. Using a cell fractionation technique we find that the major portion of daunomycin accumulates in the nucleus of both sensitive and resistant cells. Further studies reveal, however, that under efflux conditions drug is retained in the nuclei of sensitive cells but rapidly removed from the nuclei of the resistant isolate. Essentially identical results are obtained when daunomycin distribution and transport are analyzed by fluorescence microscopy. A number of agents which alter transport processes have been tested for their effect on drug accumulation in resistant cells. Thus we find that brefeldin A, which disassembles Golgi, and various lysosomotropic agents such as chloroquine and methylamine do not affect drug levels. In contrast the protonophores nigericin and monensin induce an increase in drug accumulation and inhibit efflux.

The results of this study thus suggest that resistance in HL60/Adr cells is related to a mechanism whereby drug is transported to the nucleus and thereafter rapidly redistributed to the extracellular space. The molecular basis of this transport pathway is not known.

1 Supported by Research Grant CA37585 from the National Cancer Institute, Department of Health and Human Services, and by a grant from Bristol-Myers Squibb.

2 To whom requests for reprints should be addressed, at Division of Biology, Ackert Hall, Kansas State University, Manhattan, KS 66506-4901.

Received 9/ 9/91. Accepted 3/25/92.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
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Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1992 by the American Association for Cancer Research.