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Human DNA Virus Exploitation of the MAPK-ERK Cascade

The extracellular signal-regulated kinases (ERKs) comprise a particular branch of the mitogen-activated protein kinase cascades (MAPK) that transmits extracellular signals into the intracellular environment to trigger cellular growth responses. Similar to other MAPK cascades, the MAPK-ERK pathway si...

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Detalles Bibliográficos
Autores principales: DuShane, Jeanne K., Maginnis, Melissa S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679023/
https://www.ncbi.nlm.nih.gov/pubmed/31336840
http://dx.doi.org/10.3390/ijms20143427
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author DuShane, Jeanne K.
Maginnis, Melissa S.
author_facet DuShane, Jeanne K.
Maginnis, Melissa S.
author_sort DuShane, Jeanne K.
collection PubMed
description The extracellular signal-regulated kinases (ERKs) comprise a particular branch of the mitogen-activated protein kinase cascades (MAPK) that transmits extracellular signals into the intracellular environment to trigger cellular growth responses. Similar to other MAPK cascades, the MAPK-ERK pathway signals through three core kinases—Raf, MAPK/ERK kinase (MEK), and ERK—which drive the signaling mechanisms responsible for the induction of cellular responses from extracellular stimuli including differentiation, proliferation, and cellular survival. However, pathogens like DNA viruses alter MAPK-ERK signaling in order to access DNA replication machineries, induce a proliferative state in the cell, or even prevent cell death mechanisms in response to pathogen recognition. Differential utilization of this pathway by multiple DNA viruses highlights the dynamic nature of the MAPK-ERK pathway within the cell and the importance of its function in regulating a wide variety of cellular fates that ultimately influence viral infection and, in some cases, result in tumorigenesis.
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spelling pubmed-66790232019-08-19 Human DNA Virus Exploitation of the MAPK-ERK Cascade DuShane, Jeanne K. Maginnis, Melissa S. Int J Mol Sci Review The extracellular signal-regulated kinases (ERKs) comprise a particular branch of the mitogen-activated protein kinase cascades (MAPK) that transmits extracellular signals into the intracellular environment to trigger cellular growth responses. Similar to other MAPK cascades, the MAPK-ERK pathway signals through three core kinases—Raf, MAPK/ERK kinase (MEK), and ERK—which drive the signaling mechanisms responsible for the induction of cellular responses from extracellular stimuli including differentiation, proliferation, and cellular survival. However, pathogens like DNA viruses alter MAPK-ERK signaling in order to access DNA replication machineries, induce a proliferative state in the cell, or even prevent cell death mechanisms in response to pathogen recognition. Differential utilization of this pathway by multiple DNA viruses highlights the dynamic nature of the MAPK-ERK pathway within the cell and the importance of its function in regulating a wide variety of cellular fates that ultimately influence viral infection and, in some cases, result in tumorigenesis. MDPI 2019-07-12 /pmc/articles/PMC6679023/ /pubmed/31336840 http://dx.doi.org/10.3390/ijms20143427 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
DuShane, Jeanne K.
Maginnis, Melissa S.
Human DNA Virus Exploitation of the MAPK-ERK Cascade
title Human DNA Virus Exploitation of the MAPK-ERK Cascade
title_full Human DNA Virus Exploitation of the MAPK-ERK Cascade
title_fullStr Human DNA Virus Exploitation of the MAPK-ERK Cascade
title_full_unstemmed Human DNA Virus Exploitation of the MAPK-ERK Cascade
title_short Human DNA Virus Exploitation of the MAPK-ERK Cascade
title_sort human dna virus exploitation of the mapk-erk cascade
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679023/
https://www.ncbi.nlm.nih.gov/pubmed/31336840
http://dx.doi.org/10.3390/ijms20143427
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