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MAPK pathway activation in pilocytic astrocytoma

Pilocytic astrocytoma (PA) is the most common tumor of the pediatric central nervous system (CNS). A body of research over recent years has demonstrated a key role for mitogen-activated protein kinase (MAPK) pathway signaling in the development and behavior of PAs. Several mechanisms lead to activat...

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Autores principales: Jones, David T. W., Gronych, Jan, Lichter, Peter, Witt, Olaf, Pfister, Stefan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SP Birkhäuser Verlag Basel 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350769/
https://www.ncbi.nlm.nih.gov/pubmed/22159586
http://dx.doi.org/10.1007/s00018-011-0898-9
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author Jones, David T. W.
Gronych, Jan
Lichter, Peter
Witt, Olaf
Pfister, Stefan M.
author_facet Jones, David T. W.
Gronych, Jan
Lichter, Peter
Witt, Olaf
Pfister, Stefan M.
author_sort Jones, David T. W.
collection PubMed
description Pilocytic astrocytoma (PA) is the most common tumor of the pediatric central nervous system (CNS). A body of research over recent years has demonstrated a key role for mitogen-activated protein kinase (MAPK) pathway signaling in the development and behavior of PAs. Several mechanisms lead to activation of this pathway in PA, mostly in a mutually exclusive manner, with constitutive BRAF kinase activation subsequent to gene fusion being the most frequent. The high specificity of this fusion to PA when compared with other CNS tumors has diagnostic utility. In addition, the frequency of alteration of this key pathway provides an opportunity for molecularly targeted therapy in this tumor. Here, we review the current knowledge on mechanisms of MAPK activation in PA and some of the downstream consequences of this activation, which are now starting to be elucidated both in vitro and in vivo, as well as clinical considerations and possible future directions.
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spelling pubmed-33507692012-05-30 MAPK pathway activation in pilocytic astrocytoma Jones, David T. W. Gronych, Jan Lichter, Peter Witt, Olaf Pfister, Stefan M. Cell Mol Life Sci Review Pilocytic astrocytoma (PA) is the most common tumor of the pediatric central nervous system (CNS). A body of research over recent years has demonstrated a key role for mitogen-activated protein kinase (MAPK) pathway signaling in the development and behavior of PAs. Several mechanisms lead to activation of this pathway in PA, mostly in a mutually exclusive manner, with constitutive BRAF kinase activation subsequent to gene fusion being the most frequent. The high specificity of this fusion to PA when compared with other CNS tumors has diagnostic utility. In addition, the frequency of alteration of this key pathway provides an opportunity for molecularly targeted therapy in this tumor. Here, we review the current knowledge on mechanisms of MAPK activation in PA and some of the downstream consequences of this activation, which are now starting to be elucidated both in vitro and in vivo, as well as clinical considerations and possible future directions. SP Birkhäuser Verlag Basel 2011-12-13 2012 /pmc/articles/PMC3350769/ /pubmed/22159586 http://dx.doi.org/10.1007/s00018-011-0898-9 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Review
Jones, David T. W.
Gronych, Jan
Lichter, Peter
Witt, Olaf
Pfister, Stefan M.
MAPK pathway activation in pilocytic astrocytoma
title MAPK pathway activation in pilocytic astrocytoma
title_full MAPK pathway activation in pilocytic astrocytoma
title_fullStr MAPK pathway activation in pilocytic astrocytoma
title_full_unstemmed MAPK pathway activation in pilocytic astrocytoma
title_short MAPK pathway activation in pilocytic astrocytoma
title_sort mapk pathway activation in pilocytic astrocytoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350769/
https://www.ncbi.nlm.nih.gov/pubmed/22159586
http://dx.doi.org/10.1007/s00018-011-0898-9
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