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Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours

Overactivation of the mitogen-activated protein kinase (MAPK) pathway is an important driver of many human cancers. First line, FDA-approved therapies targeting MAPK signalling, which include BRAF and MEK inhibitors, have variable success across cancers, and a significant number of patients quickly...

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Detalles Bibliográficos
Autores principales: Paton, Emily L., Turner, Jacqueline A., Schlaepfer, Isabel R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199609/
https://www.ncbi.nlm.nih.gov/pubmed/32411231
http://dx.doi.org/10.1155/2020/1079827
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author Paton, Emily L.
Turner, Jacqueline A.
Schlaepfer, Isabel R.
author_facet Paton, Emily L.
Turner, Jacqueline A.
Schlaepfer, Isabel R.
author_sort Paton, Emily L.
collection PubMed
description Overactivation of the mitogen-activated protein kinase (MAPK) pathway is an important driver of many human cancers. First line, FDA-approved therapies targeting MAPK signalling, which include BRAF and MEK inhibitors, have variable success across cancers, and a significant number of patients quickly develop resistance. In recent years, a number of preclinical studies have reported alternative methods of overcoming resistance, which include promoting apoptosis, modulating autophagy, and targeting mitochondrial metabolism. This review summarizes mechanisms of resistance to approved MAPK-targeted therapies in BRAF-mutated cancers and discusses novel preclinical approaches to overcoming resistance.
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spelling pubmed-71996092020-05-14 Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours Paton, Emily L. Turner, Jacqueline A. Schlaepfer, Isabel R. J Oncol Review Article Overactivation of the mitogen-activated protein kinase (MAPK) pathway is an important driver of many human cancers. First line, FDA-approved therapies targeting MAPK signalling, which include BRAF and MEK inhibitors, have variable success across cancers, and a significant number of patients quickly develop resistance. In recent years, a number of preclinical studies have reported alternative methods of overcoming resistance, which include promoting apoptosis, modulating autophagy, and targeting mitochondrial metabolism. This review summarizes mechanisms of resistance to approved MAPK-targeted therapies in BRAF-mutated cancers and discusses novel preclinical approaches to overcoming resistance. Hindawi 2020-01-03 /pmc/articles/PMC7199609/ /pubmed/32411231 http://dx.doi.org/10.1155/2020/1079827 Text en Copyright © 2020 Emily L. Paton et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Paton, Emily L.
Turner, Jacqueline A.
Schlaepfer, Isabel R.
Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours
title Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours
title_full Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours
title_fullStr Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours
title_full_unstemmed Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours
title_short Overcoming Resistance to Therapies Targeting the MAPK Pathway in BRAF-Mutated Tumours
title_sort overcoming resistance to therapies targeting the mapk pathway in braf-mutated tumours
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199609/
https://www.ncbi.nlm.nih.gov/pubmed/32411231
http://dx.doi.org/10.1155/2020/1079827
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