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Drug resistance in cancer: molecular evolution and compensatory proliferation

Targeted therapies have revolutionized cancer treatment. Unfortunately, their success is limited due to the development of drug resistance within the tumor, which is an evolutionary process. Understanding how drug resistance evolves is a prerequisite to a better success of targeted therapies. Resist...

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Detalles Bibliográficos
Autor principal: Friedman, Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914245/
https://www.ncbi.nlm.nih.gov/pubmed/26909596
http://dx.doi.org/10.18632/oncotarget.7459
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author Friedman, Ran
author_facet Friedman, Ran
author_sort Friedman, Ran
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description Targeted therapies have revolutionized cancer treatment. Unfortunately, their success is limited due to the development of drug resistance within the tumor, which is an evolutionary process. Understanding how drug resistance evolves is a prerequisite to a better success of targeted therapies. Resistance is usually explained as a response to evolutionary pressure imposed by treatment. Thus, evolutionary understanding can and should be used in the design and treatment of cancer. In this article, drug-resistance to targeted therapies is reviewed from an evolutionary standpoint. The concept of apoptosis-induced compensatory proliferation (AICP) is developed. It is shown that AICP helps to explain some of the phenomena that are observed experimentally in cancers. Finally, potential drug targets are suggested in light of AICP.
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spelling pubmed-49142452016-07-11 Drug resistance in cancer: molecular evolution and compensatory proliferation Friedman, Ran Oncotarget Research Perspective Targeted therapies have revolutionized cancer treatment. Unfortunately, their success is limited due to the development of drug resistance within the tumor, which is an evolutionary process. Understanding how drug resistance evolves is a prerequisite to a better success of targeted therapies. Resistance is usually explained as a response to evolutionary pressure imposed by treatment. Thus, evolutionary understanding can and should be used in the design and treatment of cancer. In this article, drug-resistance to targeted therapies is reviewed from an evolutionary standpoint. The concept of apoptosis-induced compensatory proliferation (AICP) is developed. It is shown that AICP helps to explain some of the phenomena that are observed experimentally in cancers. Finally, potential drug targets are suggested in light of AICP. Impact Journals LLC 2016-02-17 /pmc/articles/PMC4914245/ /pubmed/26909596 http://dx.doi.org/10.18632/oncotarget.7459 Text en Copyright: © 2016 Friedman http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Perspective
Friedman, Ran
Drug resistance in cancer: molecular evolution and compensatory proliferation
title Drug resistance in cancer: molecular evolution and compensatory proliferation
title_full Drug resistance in cancer: molecular evolution and compensatory proliferation
title_fullStr Drug resistance in cancer: molecular evolution and compensatory proliferation
title_full_unstemmed Drug resistance in cancer: molecular evolution and compensatory proliferation
title_short Drug resistance in cancer: molecular evolution and compensatory proliferation
title_sort drug resistance in cancer: molecular evolution and compensatory proliferation
topic Research Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914245/
https://www.ncbi.nlm.nih.gov/pubmed/26909596
http://dx.doi.org/10.18632/oncotarget.7459
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