Abstract
Drug compartmentalization as well as drug efflux can contribute to drug resistance. We demonstrate the presence of P-gp in intracellular vesicles in certain AML cell lines and show localization of DNR to a similar subcellular compartment(s) that can be altered in the presence of P-gp inhibitors. Analysis of leukaemic cell lines and 50 AML patient samples showed that the level of P-gp mRNA or total P-gp protein correlated better with drug efflux than surface P-gp protein, suggesting that intracellular P-gp may contribute to MDR in AML. Therefore, the level of total P-gp protein or mRNA may be a better indicator of MDR than surface P-gp protein. In addition, we provide evidence for a novel mechanism of drug sequestration in K562 myeloid leukaemic cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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ATP Binding Cassette Transporter, Subfamily B, Member 1 / antagonists & inhibitors
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ATP Binding Cassette Transporter, Subfamily B, Member 1 / biosynthesis
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ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism*
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ATP-Binding Cassette Transporters / metabolism
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Acute Disease
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Antibiotics, Antineoplastic / pharmacokinetics*
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Antibiotics, Antineoplastic / pharmacology
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Cell Death / drug effects
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Cell Survival
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Cyclosporine / pharmacology
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Daunorubicin / pharmacokinetics*
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Daunorubicin / pharmacology
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Dose-Response Relationship, Drug
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Drug Interactions
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Drug Resistance, Multiple
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Flow Cytometry
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HL-60 Cells
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Humans
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K562 Cells
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Leukemia, Myeloid / drug therapy
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Leukemia, Myeloid / metabolism*
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Multidrug Resistance-Associated Proteins
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Neoplasm Proteins / metabolism
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RNA, Messenger / biosynthesis
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RNA, Messenger / genetics
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Vault Ribonucleoprotein Particles / metabolism
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Verapamil / pharmacology
Substances
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ATP Binding Cassette Transporter, Subfamily B, Member 1
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ATP-Binding Cassette Transporters
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Antibiotics, Antineoplastic
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Multidrug Resistance-Associated Proteins
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Neoplasm Proteins
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RNA, Messenger
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Vault Ribonucleoprotein Particles
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major vault protein
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Cyclosporine
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Verapamil
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Daunorubicin