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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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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. |
format | Text |
id | pubmed-2830959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT freminchristophe frombasicresearchtoclinicaldevelopmentofmek12inhibitorsforcancertherapy AT melochesylvain frombasicresearchtoclinicaldevelopmentofmek12inhibitorsforcancertherapy |