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MLK4β functions as a negative regulator of MAPK signaling and cell invasion

Mixed lineage kinase (MLK) 4, or MLK4, is a member of the MLK family of mitogen-activated protein kinase kinase kinases (MAP3Ks). Typically, MAP3Ks function to activate the mitogen-activated protein kinase (MAPK)-signaling pathways and regulate different cellular responses. However, here we report t...

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Detalles Bibliográficos
Autores principales: Abi Saab, W F, Brown, M S, Chadee, D N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412637/
https://www.ncbi.nlm.nih.gov/pubmed/23552557
http://dx.doi.org/10.1038/oncsis.2012.6
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author Abi Saab, W F
Brown, M S
Chadee, D N
author_facet Abi Saab, W F
Brown, M S
Chadee, D N
author_sort Abi Saab, W F
collection PubMed
description Mixed lineage kinase (MLK) 4, or MLK4, is a member of the MLK family of mitogen-activated protein kinase kinase kinases (MAP3Ks). Typically, MAP3Ks function to activate the mitogen-activated protein kinase (MAPK)-signaling pathways and regulate different cellular responses. However, here we report that MLK4β, unlike the other MLKs, negatively regulates the activities of the MAPKs, p38, c-Jun N-terminal kinase and extracellular signal-regulated kinase, and the MAP2Ks, MEK3 and 6. Our results show that MLK4β inhibits sorbitol- and tumor necrosis factor-induced activation of p38. Furthermore, MLK4β interacts with another MLK family member, MLK3, in HCT116 cells. Exogenous expression of MLK4β inhibits activation of MLK3 and also blocks matrix metalloproteinase-9 gelatinase activity and invasion in SKOV3 ovarian cancer cells. Collectively, our data establish MLK4β as a novel suppressor of MLK3 activation, MAPK signaling and cell invasion.
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spelling pubmed-34126372012-08-13 MLK4β functions as a negative regulator of MAPK signaling and cell invasion Abi Saab, W F Brown, M S Chadee, D N Oncogenesis Original Article Mixed lineage kinase (MLK) 4, or MLK4, is a member of the MLK family of mitogen-activated protein kinase kinase kinases (MAP3Ks). Typically, MAP3Ks function to activate the mitogen-activated protein kinase (MAPK)-signaling pathways and regulate different cellular responses. However, here we report that MLK4β, unlike the other MLKs, negatively regulates the activities of the MAPKs, p38, c-Jun N-terminal kinase and extracellular signal-regulated kinase, and the MAP2Ks, MEK3 and 6. Our results show that MLK4β inhibits sorbitol- and tumor necrosis factor-induced activation of p38. Furthermore, MLK4β interacts with another MLK family member, MLK3, in HCT116 cells. Exogenous expression of MLK4β inhibits activation of MLK3 and also blocks matrix metalloproteinase-9 gelatinase activity and invasion in SKOV3 ovarian cancer cells. Collectively, our data establish MLK4β as a novel suppressor of MLK3 activation, MAPK signaling and cell invasion. Nature Publishing Group 2012-03 2012-03-26 /pmc/articles/PMC3412637/ /pubmed/23552557 http://dx.doi.org/10.1038/oncsis.2012.6 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Abi Saab, W F
Brown, M S
Chadee, D N
MLK4β functions as a negative regulator of MAPK signaling and cell invasion
title MLK4β functions as a negative regulator of MAPK signaling and cell invasion
title_full MLK4β functions as a negative regulator of MAPK signaling and cell invasion
title_fullStr MLK4β functions as a negative regulator of MAPK signaling and cell invasion
title_full_unstemmed MLK4β functions as a negative regulator of MAPK signaling and cell invasion
title_short MLK4β functions as a negative regulator of MAPK signaling and cell invasion
title_sort mlk4β functions as a negative regulator of mapk signaling and cell invasion
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412637/
https://www.ncbi.nlm.nih.gov/pubmed/23552557
http://dx.doi.org/10.1038/oncsis.2012.6
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