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Three different brain tumours evolving from a common origin
Despite an improved understanding of the molecular aberrations that occur in glioblastoma, the use of molecularly targeted therapies have so far been disappointing. We present a patient with three different brain tumours: astrocytoma, glioblastoma and gliosarcoma. Genetic analysis showed that the th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641358/ https://www.ncbi.nlm.nih.gov/pubmed/23545860 http://dx.doi.org/10.1038/oncsis.2013.1 |
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author | Forshew, T Lewis, P Waldman, A Peterson, D Glaser, M Brock, C Sheer, D Mulholland, P J |
author_facet | Forshew, T Lewis, P Waldman, A Peterson, D Glaser, M Brock, C Sheer, D Mulholland, P J |
author_sort | Forshew, T |
collection | PubMed |
description | Despite an improved understanding of the molecular aberrations that occur in glioblastoma, the use of molecularly targeted therapies have so far been disappointing. We present a patient with three different brain tumours: astrocytoma, glioblastoma and gliosarcoma. Genetic analysis showed that the three different brain tumours were derived from a common origin but had each developed unique genetic aberrations. Included in these, the glioblastoma had PDGFRA amplification, whereas the gliosarcoma had MYC amplification. We propose that genetic heterogeneity contributes to treatment failure and requires comprehensive assessment in the era of personalised medicine. |
format | Online Article Text |
id | pubmed-3641358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36413582013-05-02 Three different brain tumours evolving from a common origin Forshew, T Lewis, P Waldman, A Peterson, D Glaser, M Brock, C Sheer, D Mulholland, P J Oncogenesis Original Article Despite an improved understanding of the molecular aberrations that occur in glioblastoma, the use of molecularly targeted therapies have so far been disappointing. We present a patient with three different brain tumours: astrocytoma, glioblastoma and gliosarcoma. Genetic analysis showed that the three different brain tumours were derived from a common origin but had each developed unique genetic aberrations. Included in these, the glioblastoma had PDGFRA amplification, whereas the gliosarcoma had MYC amplification. We propose that genetic heterogeneity contributes to treatment failure and requires comprehensive assessment in the era of personalised medicine. Nature Publishing Group 2013-04 2013-04-01 /pmc/articles/PMC3641358/ /pubmed/23545860 http://dx.doi.org/10.1038/oncsis.2013.1 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Forshew, T Lewis, P Waldman, A Peterson, D Glaser, M Brock, C Sheer, D Mulholland, P J Three different brain tumours evolving from a common origin |
title | Three different brain tumours evolving from a common origin |
title_full | Three different brain tumours evolving from a common origin |
title_fullStr | Three different brain tumours evolving from a common origin |
title_full_unstemmed | Three different brain tumours evolving from a common origin |
title_short | Three different brain tumours evolving from a common origin |
title_sort | three different brain tumours evolving from a common origin |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641358/ https://www.ncbi.nlm.nih.gov/pubmed/23545860 http://dx.doi.org/10.1038/oncsis.2013.1 |
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