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From basic research to clinical development of MEK1/2 inhibitors for cancer therapy

The Ras-dependent Raf/MEK/ERK1/2 mitogen-activated protein (MAP) kinase signaling pathway is a major regulator of cell proliferation and survival. Not surprisingly, hyperactivation of this pathway is frequently observed in human malignancies as a result of aberrant activation of receptor tyrosine ki...

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Detalles Bibliográficos
Autores principales: Frémin, Christophe, Meloche, Sylvain
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2830959/
https://www.ncbi.nlm.nih.gov/pubmed/20149254
http://dx.doi.org/10.1186/1756-8722-3-8
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author Frémin, Christophe
Meloche, Sylvain
author_facet Frémin, Christophe
Meloche, Sylvain
author_sort Frémin, Christophe
collection PubMed
description The Ras-dependent Raf/MEK/ERK1/2 mitogen-activated protein (MAP) kinase signaling pathway is a major regulator of cell proliferation and survival. Not surprisingly, hyperactivation of this pathway is frequently observed in human malignancies as a result of aberrant activation of receptor tyrosine kinases or gain-of-function mutations in RAS or RAF genes. Components of the ERK1/2 pathway are therefore viewed as attractive candidates for the development of targeted therapies of cancer. In this article, we briefly review the basic research that has laid the groundwork for the clinical development of small molecules inhibitors of the ERK1/2 pathway. We then present the current state of clinical evaluation of MEK1/2 inhibitors in cancer and discuss challenges ahead.
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spelling pubmed-28309592010-03-03 From basic research to clinical development of MEK1/2 inhibitors for cancer therapy Frémin, Christophe Meloche, Sylvain J Hematol Oncol Review The Ras-dependent Raf/MEK/ERK1/2 mitogen-activated protein (MAP) kinase signaling pathway is a major regulator of cell proliferation and survival. Not surprisingly, hyperactivation of this pathway is frequently observed in human malignancies as a result of aberrant activation of receptor tyrosine kinases or gain-of-function mutations in RAS or RAF genes. Components of the ERK1/2 pathway are therefore viewed as attractive candidates for the development of targeted therapies of cancer. In this article, we briefly review the basic research that has laid the groundwork for the clinical development of small molecules inhibitors of the ERK1/2 pathway. We then present the current state of clinical evaluation of MEK1/2 inhibitors in cancer and discuss challenges ahead. BioMed Central 2010-02-11 /pmc/articles/PMC2830959/ /pubmed/20149254 http://dx.doi.org/10.1186/1756-8722-3-8 Text en Copyright ©2010 Frémin and Meloche; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Frémin, Christophe
Meloche, Sylvain
From basic research to clinical development of MEK1/2 inhibitors for cancer therapy
title From basic research to clinical development of MEK1/2 inhibitors for cancer therapy
title_full From basic research to clinical development of MEK1/2 inhibitors for cancer therapy
title_fullStr From basic research to clinical development of MEK1/2 inhibitors for cancer therapy
title_full_unstemmed From basic research to clinical development of MEK1/2 inhibitors for cancer therapy
title_short From basic research to clinical development of MEK1/2 inhibitors for cancer therapy
title_sort from basic research to clinical development of mek1/2 inhibitors for cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2830959/
https://www.ncbi.nlm.nih.gov/pubmed/20149254
http://dx.doi.org/10.1186/1756-8722-3-8
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