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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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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 |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-4914245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT friedmanran drugresistanceincancermolecularevolutionandcompensatoryproliferation |