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Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5

Perturbed action of signal transduction pathways, including the mitogen-activated protein (MAP) kinase pathways, is one of the hallmarks of many cancers. While the implication of the typical MAP kinase pathways ERK1/2-MEK1/2, p38(MAPK) and JNK is well established, recent findings illustrate that the...

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Autores principales: Kostenko, Sergiy, Dumitriu, Gianina, Moens, Ugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419095/
https://www.ncbi.nlm.nih.gov/pubmed/22800433
http://dx.doi.org/10.1186/1750-2187-7-9
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author Kostenko, Sergiy
Dumitriu, Gianina
Moens, Ugo
author_facet Kostenko, Sergiy
Dumitriu, Gianina
Moens, Ugo
author_sort Kostenko, Sergiy
collection PubMed
description Perturbed action of signal transduction pathways, including the mitogen-activated protein (MAP) kinase pathways, is one of the hallmarks of many cancers. While the implication of the typical MAP kinase pathways ERK1/2-MEK1/2, p38(MAPK) and JNK is well established, recent findings illustrate that the atypical MAP kinase ERK3/4-MK5 may also be involved in tumorigenic processes. Remarkably, the ERK3/4-MK5 pathway seems to possess anti-oncogenic as well as pro-oncogenic properties in cell culture and aninal models. This review summarizes the mutations in the genes encoding ERK3, ERK4 and MK5 that have been detected in different cancers, reports aberrant expression levels of these proteins in human tumours, and discusses the mechanisms by which this pathway can induce senescence, stimulate angiogenesis and invasiveness.
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spelling pubmed-34190952012-08-15 Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5 Kostenko, Sergiy Dumitriu, Gianina Moens, Ugo J Mol Signal Review Perturbed action of signal transduction pathways, including the mitogen-activated protein (MAP) kinase pathways, is one of the hallmarks of many cancers. While the implication of the typical MAP kinase pathways ERK1/2-MEK1/2, p38(MAPK) and JNK is well established, recent findings illustrate that the atypical MAP kinase ERK3/4-MK5 may also be involved in tumorigenic processes. Remarkably, the ERK3/4-MK5 pathway seems to possess anti-oncogenic as well as pro-oncogenic properties in cell culture and aninal models. This review summarizes the mutations in the genes encoding ERK3, ERK4 and MK5 that have been detected in different cancers, reports aberrant expression levels of these proteins in human tumours, and discusses the mechanisms by which this pathway can induce senescence, stimulate angiogenesis and invasiveness. BioMed Central 2012-07-16 /pmc/articles/PMC3419095/ /pubmed/22800433 http://dx.doi.org/10.1186/1750-2187-7-9 Text en Copyright ©2012 Kostenko et al.; 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
Kostenko, Sergiy
Dumitriu, Gianina
Moens, Ugo
Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5
title Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5
title_full Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5
title_fullStr Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5
title_full_unstemmed Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5
title_short Tumour promoting and suppressing roles of the atypical MAP kinase signalling pathway ERK3/4-MK5
title_sort tumour promoting and suppressing roles of the atypical map kinase signalling pathway erk3/4-mk5
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419095/
https://www.ncbi.nlm.nih.gov/pubmed/22800433
http://dx.doi.org/10.1186/1750-2187-7-9
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