P-glycoprotein-mediated transcellular transport of MDR-reversing agents.
Article Details
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Citation
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Saeki T, Ueda K, Tanigawara Y, Hori R, Komano T
P-glycoprotein-mediated transcellular transport of MDR-reversing agents.
FEBS Lett. 1993 Jun 7;324(1):99-102.
- PubMed ID
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8099333 [View in PubMed]
- Abstract
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Understanding of the interactions between P-glycoprotein and multidrug resistance (MDR) reversing agents is important in designing more effective MDR modulators. We examined transcellular transport of several MDR modulators by using a drug-sensitive epithelial cell line, LLC-PK1, and its transformant cell line, LLC-GA5-COL300, which expresses human P-glycoprotein on the apical surface. Basal-to-apical transports of azidopine and diltiazem across the LLC-GA5-COL300 monolayer were increased and apical-to-basal transports were decreased compared to those across the LLC-PK1 monolayer, indicating that P-glycoprotein transports azidopine and diltiazem. Movements of nitrendipine and staurosporine across the epithelial monolayer were not affected by P-glycoprotein. These results suggests that some MDR modulators exert their inhibitory effect not only by blocking the initial binding of anticancer drugs but throughout the course of the transport process.
DrugBank Data that Cites this Article
- 药物转运蛋白
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Drug Transporter Kind Organism Pharmacological Action Actions Diltiazem P-glycoprotein 1 Protein Humans UnknownSubstrateInhibitorDetails