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Efflux pump proteins in antifungal resistance

It is now well-known that the enhanced expression of ATP binding cassette (ABC) and major facilitator superfamily (MFS) proteins contribute to the development of tolerance to antifungals in yeasts. For example, the azole resistant clinical isolates of the opportunistic human fungal pathogen Candida...

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Detalles Bibliográficos
Autores principales: Prasad, Rajendra, Rawal, Manpreet K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148622/
https://www.ncbi.nlm.nih.gov/pubmed/25221515
http://dx.doi.org/10.3389/fphar.2014.00202
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author Prasad, Rajendra
Rawal, Manpreet K.
author_facet Prasad, Rajendra
Rawal, Manpreet K.
author_sort Prasad, Rajendra
collection PubMed
description It is now well-known that the enhanced expression of ATP binding cassette (ABC) and major facilitator superfamily (MFS) proteins contribute to the development of tolerance to antifungals in yeasts. For example, the azole resistant clinical isolates of the opportunistic human fungal pathogen Candida albicans show an overexpression of Cdr1p and/or CaMdr1p belonging to ABC and MFS superfamilies, respectively. Hence, azole resistant isolates display reduced accumulation of therapeutic drug due to its rapid extrusion and that facilitates its survival. Considering the importance of major antifungal transporters, the focus of recent research has been to understand the structure and function of these proteins to design inhibitors/modulators to block the pump protein activity so that the drug already in use could again sensitize resistant yeast cells. The review focuses on the structure and function of ABC and MFS transporters of Candida to highlight the recent advancement in the field.
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spelling pubmed-41486222014-09-12 Efflux pump proteins in antifungal resistance Prasad, Rajendra Rawal, Manpreet K. Front Pharmacol Pharmacology It is now well-known that the enhanced expression of ATP binding cassette (ABC) and major facilitator superfamily (MFS) proteins contribute to the development of tolerance to antifungals in yeasts. For example, the azole resistant clinical isolates of the opportunistic human fungal pathogen Candida albicans show an overexpression of Cdr1p and/or CaMdr1p belonging to ABC and MFS superfamilies, respectively. Hence, azole resistant isolates display reduced accumulation of therapeutic drug due to its rapid extrusion and that facilitates its survival. Considering the importance of major antifungal transporters, the focus of recent research has been to understand the structure and function of these proteins to design inhibitors/modulators to block the pump protein activity so that the drug already in use could again sensitize resistant yeast cells. The review focuses on the structure and function of ABC and MFS transporters of Candida to highlight the recent advancement in the field. Frontiers Media S.A. 2014-08-29 /pmc/articles/PMC4148622/ /pubmed/25221515 http://dx.doi.org/10.3389/fphar.2014.00202 Text en Copyright © 2014 Prasad and Rawal. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Prasad, Rajendra
Rawal, Manpreet K.
Efflux pump proteins in antifungal resistance
title Efflux pump proteins in antifungal resistance
title_full Efflux pump proteins in antifungal resistance
title_fullStr Efflux pump proteins in antifungal resistance
title_full_unstemmed Efflux pump proteins in antifungal resistance
title_short Efflux pump proteins in antifungal resistance
title_sort efflux pump proteins in antifungal resistance
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148622/
https://www.ncbi.nlm.nih.gov/pubmed/25221515
http://dx.doi.org/10.3389/fphar.2014.00202
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