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Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma

The advent of genomics has led to the identification of specific “driver” mutations in oncogenic kinases, and the development of targeted small molecule inhibitors to block their tumor-driving functions. These specific inhibitors have been a clinical success, and often significantly prolong the live...

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Autores principales: Neel, Dana S., Bivona, Trever G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687582/
https://www.ncbi.nlm.nih.gov/pubmed/29152593
http://dx.doi.org/10.1038/s41698-017-0007-0
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author Neel, Dana S.
Bivona, Trever G.
author_facet Neel, Dana S.
Bivona, Trever G.
author_sort Neel, Dana S.
collection PubMed
description The advent of genomics has led to the identification of specific “driver” mutations in oncogenic kinases, and the development of targeted small molecule inhibitors to block their tumor-driving functions. These specific inhibitors have been a clinical success, and often significantly prolong the lives of individuals with cancer. Inevitably, however, the treated tumors recur as resistance to these targeted therapies develops. Here, we review the major mechanisms by which a cancer cell can evade targeted therapy, focusing on mechanisms of resistance to kinase inhibitors in lung cancer. We discuss the promising concept of rational upfront polytherapy in lung cancer, which involves concurrently targeting multiple proteins in critical signaling pathways in a cancer cell to prevent or delay resistance.
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spelling pubmed-56875822017-11-15 Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma Neel, Dana S. Bivona, Trever G. NPJ Precis Oncol Review Article The advent of genomics has led to the identification of specific “driver” mutations in oncogenic kinases, and the development of targeted small molecule inhibitors to block their tumor-driving functions. These specific inhibitors have been a clinical success, and often significantly prolong the lives of individuals with cancer. Inevitably, however, the treated tumors recur as resistance to these targeted therapies develops. Here, we review the major mechanisms by which a cancer cell can evade targeted therapy, focusing on mechanisms of resistance to kinase inhibitors in lung cancer. We discuss the promising concept of rational upfront polytherapy in lung cancer, which involves concurrently targeting multiple proteins in critical signaling pathways in a cancer cell to prevent or delay resistance. Nature Publishing Group UK 2017-03-20 /pmc/articles/PMC5687582/ /pubmed/29152593 http://dx.doi.org/10.1038/s41698-017-0007-0 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Review Article
Neel, Dana S.
Bivona, Trever G.
Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma
title Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma
title_full Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma
title_fullStr Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma
title_full_unstemmed Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma
title_short Resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma
title_sort resistance is futile: overcoming resistance to targeted therapies in lung adenocarcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5687582/
https://www.ncbi.nlm.nih.gov/pubmed/29152593
http://dx.doi.org/10.1038/s41698-017-0007-0
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