Fluorimetric Methods for Analysis of Permeability, Drug Transport Kinetics, and Inhibition of the ABCB1 Membrane Transporter
The cell membrane P-glycoprotein (P-gp; MDR1, ABCB1) is an energy-dependent efflux pump that belongs to the ATP-binding cassette (ABC) family of transporters, and has been associated with drug resistance in eukaryotic cells. Multidrug resistance (MDR) is related to an increased expression and functi...
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| Dokumentumtípus: | Könyv része |
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Springer New York
New York
2016
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| Sorozat: | Methods in Molecular Biology
1395 METHODS IN MOLECULAR BIOLOGY 1395 Cancer Drug Resistance : Overviews and Methods 1395 |
| doi: | 10.1007/978-1-4939-3347-1_7 |
| mtmt: | 3026841 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/10420 |
| LEADER | 02889naa a2200313 i 4500 | ||
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| 008 | 170202s2016 hu o 0|| zxx d | ||
| 020 | |a 9781493933457 | ||
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| 024 | 7 | |a 10.1007/978-1-4939-3347-1_7 |2 doi | |
| 024 | 7 | |a 3026841 |2 mtmt | |
| 040 | |a SZTE Publicatio Repozitórium |b hun | ||
| 041 | |a zxx | ||
| 100 | 1 | |a Armada Ana | |
| 245 | 1 | 0 | |a Fluorimetric Methods for Analysis of Permeability, Drug Transport Kinetics, and Inhibition of the ABCB1 Membrane Transporter |h [elektronikus dokumentum] / |c Armada Ana |
| 260 | |a Springer New York |b New York |c 2016 | ||
| 300 | |a 87-103 | ||
| 490 | 0 | |a Methods in Molecular Biology |v 1395 | |
| 490 | 0 | |a METHODS IN MOLECULAR BIOLOGY |v 1395 | |
| 490 | 0 | |a Cancer Drug Resistance : Overviews and Methods |v 1395 | |
| 520 | 3 | |a The cell membrane P-glycoprotein (P-gp; MDR1, ABCB1) is an energy-dependent efflux pump that belongs to the ATP-binding cassette (ABC) family of transporters, and has been associated with drug resistance in eukaryotic cells. Multidrug resistance (MDR) is related to an increased expression and function of the ABCB1 (P-gp) efflux pump that often causes chemotherapeutic failure in cancer. Modulators of this efflux pump, such as the calcium channel blocker verapamil (VP) and cyclosporine A (CypA), can reverse the MDR phenotype but in vivo studies have revealed disappointing results due to adverse side effects. Currently available methods are unable to visualize and assess in a real-time basis the effectiveness of ABCB1 inhibitors on the uptake and efflux of ABCB1 substrates. However, predicting and testing ABCB1 modulation activity using living cells during drug development are crucial. The use of ABCB1-transfected mouse T-lymphoma cell line to study the uptake/efflux of fluorescent probes like ethidium bromide (EB), rhodamine 123 (Rh-123), and carbocyanine dye DiOC2, in the presence and absence of potential inhibitors, is currently used in our laboratories to evaluate the ability of a drug to inhibit ABCB1-mediated drug accumulation and efflux. Here we describe and compare three in vitro methods, which evaluate the permeability, transport kinetics of fluorescent substrates, and inhibition of the ABCB1 efflux pump by drugs of chemical synthesis or extracted from natural sources, using model cancer cell lines overexpressing this transporter, namely (1) real-time fluorimetry that assesses the accumulation of ethidium bromide, (2) flow cytometry, and (3) fluorescent microscopy using rhodamine 123 and DiOC2. | |
| 700 | 0 | 1 | |a Martins Célia |e aut |
| 700 | 0 | 1 | |a Spengler Gabriella |e aut |
| 700 | 0 | 1 | |a Molnár József |e aut |
| 700 | 0 | 1 | |a Amaral Leonard |e aut |
| 700 | 0 | 1 | |a Rodrigues António Sebastião |e aut |
| 700 | 0 | 1 | |a Viveiros Miguel |e aut |
| 856 | 4 | 0 | |u http://publicatio.bibl.u-szeged.hu/10420/1/Armada_et_al_MethMolBio_2016.pdf |z Dokumentum-elérés |