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Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology

Multidrug resistance (MDR), which significantly decreases the efficacy of anticancer drugs and causes tumor recurrence, has been a major challenge in clinical cancer treatment with chemotherapeutic drugs for decades. Several mechanisms of overcoming drug resistance have been postulated. Well known P...

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Detalles Bibliográficos
Autores principales: Xue, Xue, Liang, Xing-Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777470/
https://www.ncbi.nlm.nih.gov/pubmed/22237039
http://dx.doi.org/10.5732/cjc.011.10326
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author Xue, Xue
Liang, Xing-Jie
author_facet Xue, Xue
Liang, Xing-Jie
author_sort Xue, Xue
collection PubMed
description Multidrug resistance (MDR), which significantly decreases the efficacy of anticancer drugs and causes tumor recurrence, has been a major challenge in clinical cancer treatment with chemotherapeutic drugs for decades. Several mechanisms of overcoming drug resistance have been postulated. Well known P-glycoprotein (P-gp) and other drug efflux transporters are considered to be critical in pumping anticancer drugs out of cells and causing chemotherapy failure. Innovative theranostic (therapeutic and diagnostic) strategies with nanoparticles are rapidly evolving and are anticipated to offer opportunities to overcome these limits. In this review, we discuss the mechanisms of drug efflux-mediated resistance and the application of multiple nanoparticle-based platforms to overcome chemoresistance and improve therapeutic outcome.
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spelling pubmed-37774702013-12-11 Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology Xue, Xue Liang, Xing-Jie Chin J Cancer Review Multidrug resistance (MDR), which significantly decreases the efficacy of anticancer drugs and causes tumor recurrence, has been a major challenge in clinical cancer treatment with chemotherapeutic drugs for decades. Several mechanisms of overcoming drug resistance have been postulated. Well known P-glycoprotein (P-gp) and other drug efflux transporters are considered to be critical in pumping anticancer drugs out of cells and causing chemotherapy failure. Innovative theranostic (therapeutic and diagnostic) strategies with nanoparticles are rapidly evolving and are anticipated to offer opportunities to overcome these limits. In this review, we discuss the mechanisms of drug efflux-mediated resistance and the application of multiple nanoparticle-based platforms to overcome chemoresistance and improve therapeutic outcome. Sun Yat-sen University Cancer Center 2012-02 /pmc/articles/PMC3777470/ /pubmed/22237039 http://dx.doi.org/10.5732/cjc.011.10326 Text en Chinese Journal of Cancer http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Review
Xue, Xue
Liang, Xing-Jie
Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology
title Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology
title_full Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology
title_fullStr Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology
title_full_unstemmed Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology
title_short Overcoming drug efflux-based multidrug resistance in cancer with nanotechnology
title_sort overcoming drug efflux-based multidrug resistance in cancer with nanotechnology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777470/
https://www.ncbi.nlm.nih.gov/pubmed/22237039
http://dx.doi.org/10.5732/cjc.011.10326
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