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“RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway

The Raf/Mek/Erk signaling pathway, activated downstream of Ras primarily to promote proliferation, represents the best studied of the evolutionary conserved MAPK cascades. The investigation of the pathway has continued unabated since its discovery roughly 30 years ago. In the last decade, however, t...

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Detalles Bibliográficos
Autores principales: Cseh, Botond, Doma, Eszter, Baccarini, Manuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099524/
https://www.ncbi.nlm.nih.gov/pubmed/24937142
http://dx.doi.org/10.1016/j.febslet.2014.06.025
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author Cseh, Botond
Doma, Eszter
Baccarini, Manuela
author_facet Cseh, Botond
Doma, Eszter
Baccarini, Manuela
author_sort Cseh, Botond
collection PubMed
description The Raf/Mek/Erk signaling pathway, activated downstream of Ras primarily to promote proliferation, represents the best studied of the evolutionary conserved MAPK cascades. The investigation of the pathway has continued unabated since its discovery roughly 30 years ago. In the last decade, however, the identification of unexpected in vivo functions of pathway components, as well as the discovery of Raf mutations in human cancer, the ensuing quest for inhibitors, and the efforts to understand their mechanism of action, have boosted interest tremendously. From this large body of work, protein–protein interaction has emerged as a recurrent, crucial theme. This review focuses on the role of protein complexes in the regulation of the Raf/Mek/Erk pathway and in its cross-talk with other signaling cascades. Mapping these interactions and finding a way of exploiting them for therapeutic purposes is one of the challenges of future molecule-targeted therapy.
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spelling pubmed-40995242014-08-01 “RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway Cseh, Botond Doma, Eszter Baccarini, Manuela FEBS Lett Review The Raf/Mek/Erk signaling pathway, activated downstream of Ras primarily to promote proliferation, represents the best studied of the evolutionary conserved MAPK cascades. The investigation of the pathway has continued unabated since its discovery roughly 30 years ago. In the last decade, however, the identification of unexpected in vivo functions of pathway components, as well as the discovery of Raf mutations in human cancer, the ensuing quest for inhibitors, and the efforts to understand their mechanism of action, have boosted interest tremendously. From this large body of work, protein–protein interaction has emerged as a recurrent, crucial theme. This review focuses on the role of protein complexes in the regulation of the Raf/Mek/Erk pathway and in its cross-talk with other signaling cascades. Mapping these interactions and finding a way of exploiting them for therapeutic purposes is one of the challenges of future molecule-targeted therapy. Elsevier Science B.V 2014-08-01 /pmc/articles/PMC4099524/ /pubmed/24937142 http://dx.doi.org/10.1016/j.febslet.2014.06.025 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Cseh, Botond
Doma, Eszter
Baccarini, Manuela
“RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway
title “RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway
title_full “RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway
title_fullStr “RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway
title_full_unstemmed “RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway
title_short “RAF” neighborhood: Protein–protein interaction in the Raf/Mek/Erk pathway
title_sort “raf” neighborhood: protein–protein interaction in the raf/mek/erk pathway
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099524/
https://www.ncbi.nlm.nih.gov/pubmed/24937142
http://dx.doi.org/10.1016/j.febslet.2014.06.025
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