Abstract
We examined the effects of suppressing multidrug resistance-associated protein 1 (MRP1) gene expression in a human glioma cell line U87MG. Hammerhead ribozymes, designed to cleave MRP1 mRNA (alphaMRP1-Rz), were transfected into the U87MG cells. The U87MG/alphaMRP1-Rz cells were significantly sensitive to nitrosourea (ACNU) and doxorubicin (DOX) compared with the U87MG cells (p<0.01 and p<0.05, respectively, unpaired t-test). There was no significant difference in the expression of other human genes between the U87MG/alphaMRP1-Rz and controls by cDNA array. The hammerhead ribozyme-mediated specific suppression of MRP1 was sufficient to reverse the resistance of ACNU and DOX in the human glioma cell line.
MeSH terms
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Antibiotics, Antineoplastic / pharmacology
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Blotting, Northern
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Cell Division
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Cell Line, Tumor
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Cell-Free System
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Coloring Agents / pharmacology
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DNA, Complementary / metabolism
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Doxorubicin / pharmacology
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Drug Resistance, Multiple*
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Gene Expression Regulation
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Humans
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Inhibitory Concentration 50
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Nitrosourea Compounds / pharmacology
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Oligonucleotide Array Sequence Analysis
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RNA, Catalytic* / chemistry
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RNA, Catalytic* / metabolism
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RNA, Messenger / metabolism
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Tetrazolium Salts / pharmacology
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Thiazoles / pharmacology
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Transfection
Substances
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Antibiotics, Antineoplastic
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Coloring Agents
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DNA, Complementary
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Nitrosourea Compounds
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RNA, Catalytic
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RNA, Messenger
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Tetrazolium Salts
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Thiazoles
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hammerhead ribozyme
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Doxorubicin
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thiazolyl blue