Abstract
Cellular drug resistance is believed to involve P-glycoprotein-related drug efflux as well as xenobiotic detoxification. In the present study, we analyzed five human melanoma cell lines with 1- to 6-fold doxorubicin resistance for doxorubicin retention and MDR-1 and GST pi gene expression. All the cell lines had high doxorubicin retention, and efflux blockers such as trifluoperazine and verapamil did not have a major effect on drug retention or cytotoxicity. Even though all the cell lines carried the MDR-1 and GST pi genes, gene amplification was not associated with drug resistance. Both laser flow cytometry and immunoperoxidase staining showed high expression of C-219 reactive P-glycoprotein in some of the resistant cells which was not accompanied by either high drug efflux or sensitivity to doxorubicin efflux blockers.
Publication types
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Comparative Study
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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ATP Binding Cassette Transporter, Subfamily B, Member 1
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Animals
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Cell Death / drug effects
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Cell Division / drug effects
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Cell Line / drug effects
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Cricetinae
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Cricetulus
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Dose-Response Relationship, Drug
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Doxorubicin / pharmacology*
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Drug Resistance / genetics
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Gene Expression
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Glutathione Transferase / analysis*
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Glutathione Transferase / genetics
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Humans
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Leukemia P388 / genetics
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Melanoma / genetics*
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Membrane Glycoproteins / analysis*
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Membrane Glycoproteins / genetics
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Mice
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RNA, Messenger / analysis
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Trifluoperazine / pharmacology
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Tumor Cells, Cultured / drug effects
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Verapamil / pharmacology
Substances
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ATP Binding Cassette Transporter, Subfamily B, Member 1
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Membrane Glycoproteins
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RNA, Messenger
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Trifluoperazine
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Doxorubicin
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Verapamil
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Glutathione Transferase