Abstract
Enhanced expression of a multidrug-resistance gene (MDR1) is observed in some cancer patient, but any regulatory mechanisms of MDR1 gene expression in this phenomenon is not yet known. In this study, the regulation of MDR1 gene was analysed by transient expression assays in the presence of anticancer agents. We found that MDR1 promoter could be activated directly on the addition of anticancer agents including vincristine, daunomycin, adriamycin and colchicine. The results suggest that the level of MDR1 mRNA expression is associated with previous chemotherapy, including drugs that select the multidrug resistance phenotype.
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
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Animals
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Antineoplastic Agents / pharmacology*
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Cell Line
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Chloramphenicol O-Acetyltransferase / genetics
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Chlorocebus aethiops
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Colchicine / pharmacology
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Daunorubicin / pharmacology
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Doxorubicin / pharmacology
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Drug Resistance / genetics*
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Gene Expression Regulation / drug effects*
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Humans
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Kidney
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Membrane Glycoproteins / genetics
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Plasmids
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Promoter Regions, Genetic / genetics
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RNA, Messenger / genetics
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Restriction Mapping
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Transfection
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Tumor Cells, Cultured
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Vincristine / pharmacology
Substances
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ATP Binding Cassette Transporter, Subfamily B, Member 1
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Antineoplastic Agents
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Membrane Glycoproteins
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RNA, Messenger
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Vincristine
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Doxorubicin
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Chloramphenicol O-Acetyltransferase
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Colchicine
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Daunorubicin