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Mechanisms and insights into drug resistance in cancer

Cancer drug resistance continues to be a major impediment in medical oncology. Clinically, resistance can arise prior to or as a result of cancer therapy. In this review, we discuss different mechanisms adapted by cancerous cells to resist treatment, including alteration in drug transport and metabo...

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Detalles Bibliográficos
Autores principales: Zahreddine, Hiba, Borden, Katherine L. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596793/
https://www.ncbi.nlm.nih.gov/pubmed/23504227
http://dx.doi.org/10.3389/fphar.2013.00028
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author Zahreddine, Hiba
Borden, Katherine L. B.
author_facet Zahreddine, Hiba
Borden, Katherine L. B.
author_sort Zahreddine, Hiba
collection PubMed
description Cancer drug resistance continues to be a major impediment in medical oncology. Clinically, resistance can arise prior to or as a result of cancer therapy. In this review, we discuss different mechanisms adapted by cancerous cells to resist treatment, including alteration in drug transport and metabolism, mutation and amplification of drug targets, as well as genetic rewiring which can lead to impaired apoptosis. Tumor heterogeneity may also contribute to resistance, where small subpopulations of cells may acquire or stochastically already possess some of the features enabling them to emerge under selective drug pressure. Making the problem even more challenging, some of these resistance pathways lead to multidrug resistance, generating an even more difficult clinical problem to overcome. We provide examples of these mechanisms and some insights into how understanding these processes can influence the next generation of cancer therapies.
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spelling pubmed-35967932013-03-15 Mechanisms and insights into drug resistance in cancer Zahreddine, Hiba Borden, Katherine L. B. Front Pharmacol Pharmacology Cancer drug resistance continues to be a major impediment in medical oncology. Clinically, resistance can arise prior to or as a result of cancer therapy. In this review, we discuss different mechanisms adapted by cancerous cells to resist treatment, including alteration in drug transport and metabolism, mutation and amplification of drug targets, as well as genetic rewiring which can lead to impaired apoptosis. Tumor heterogeneity may also contribute to resistance, where small subpopulations of cells may acquire or stochastically already possess some of the features enabling them to emerge under selective drug pressure. Making the problem even more challenging, some of these resistance pathways lead to multidrug resistance, generating an even more difficult clinical problem to overcome. We provide examples of these mechanisms and some insights into how understanding these processes can influence the next generation of cancer therapies. Frontiers Media S.A. 2013-03-14 /pmc/articles/PMC3596793/ /pubmed/23504227 http://dx.doi.org/10.3389/fphar.2013.00028 Text en Copyright © Zahreddine and Borden. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Pharmacology
Zahreddine, Hiba
Borden, Katherine L. B.
Mechanisms and insights into drug resistance in cancer
title Mechanisms and insights into drug resistance in cancer
title_full Mechanisms and insights into drug resistance in cancer
title_fullStr Mechanisms and insights into drug resistance in cancer
title_full_unstemmed Mechanisms and insights into drug resistance in cancer
title_short Mechanisms and insights into drug resistance in cancer
title_sort mechanisms and insights into drug resistance in cancer
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596793/
https://www.ncbi.nlm.nih.gov/pubmed/23504227
http://dx.doi.org/10.3389/fphar.2013.00028
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