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Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme

The purpose of this study was to investigate the molecular background of cerebral blood volume (CBV) and vessel size (VS) of capillaries in glioblastoma multiforme (GBM). Both parameters are derived from extended perfusion MR imaging. A prospective case study including 21 patients (median age 66 yea...

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Autores principales: Heiland, Dieter Henrik, Demerath, Theo, Kellner, Elias, Kiselev, Valerij G., Pfeifer, Dietmar, Schnell, Oliver, Staszewski, Ori, Urbach, Horst, Weyerbrock, Astrid, Mader, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355248/
https://www.ncbi.nlm.nih.gov/pubmed/27613830
http://dx.doi.org/10.18632/oncotarget.11522
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author Heiland, Dieter Henrik
Demerath, Theo
Kellner, Elias
Kiselev, Valerij G.
Pfeifer, Dietmar
Schnell, Oliver
Staszewski, Ori
Urbach, Horst
Weyerbrock, Astrid
Mader, Irina
author_facet Heiland, Dieter Henrik
Demerath, Theo
Kellner, Elias
Kiselev, Valerij G.
Pfeifer, Dietmar
Schnell, Oliver
Staszewski, Ori
Urbach, Horst
Weyerbrock, Astrid
Mader, Irina
author_sort Heiland, Dieter Henrik
collection PubMed
description The purpose of this study was to investigate the molecular background of cerebral blood volume (CBV) and vessel size (VS) of capillaries in glioblastoma multiforme (GBM). Both parameters are derived from extended perfusion MR imaging. A prospective case study including 21 patients (median age 66 years, 10 females) was performed. Before operation, CBV and VS of contrast enhancing tumor were assessed. Tissue was sampled from the assessed areas under neuronavigation control. After RNA extraction, transcriptional data was analyzed by Weighted Gene Co-Expression Network Analysis (WGCNA) and split into modules based on its network affiliations. Gene Set Enrichment Analysis (GSEA) identified biological functions or pathways of the genetic modules. These were applied on 484 GBM samples of the TCGA database. Ten modules were highly correlated to CBV and VS. One module was exclusively associated to VS and highly correlated to hypoxia, another one exclusively to CBV showing strong enrichments in the Epithelial Growth Factor (EGF) pathway and Epithelial-to-Mesenchymal-Transition (EMT). Moreover, patients with increased CBV and VS predominantly showed a mesenchymal gene-expression, a finding that could be corroborated by TCGA data. In conclusion, CBV and VS mirror different genetic pathways and reflect certain molecular subclasses of GBM.
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spelling pubmed-53552482017-04-26 Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme Heiland, Dieter Henrik Demerath, Theo Kellner, Elias Kiselev, Valerij G. Pfeifer, Dietmar Schnell, Oliver Staszewski, Ori Urbach, Horst Weyerbrock, Astrid Mader, Irina Oncotarget Research Paper The purpose of this study was to investigate the molecular background of cerebral blood volume (CBV) and vessel size (VS) of capillaries in glioblastoma multiforme (GBM). Both parameters are derived from extended perfusion MR imaging. A prospective case study including 21 patients (median age 66 years, 10 females) was performed. Before operation, CBV and VS of contrast enhancing tumor were assessed. Tissue was sampled from the assessed areas under neuronavigation control. After RNA extraction, transcriptional data was analyzed by Weighted Gene Co-Expression Network Analysis (WGCNA) and split into modules based on its network affiliations. Gene Set Enrichment Analysis (GSEA) identified biological functions or pathways of the genetic modules. These were applied on 484 GBM samples of the TCGA database. Ten modules were highly correlated to CBV and VS. One module was exclusively associated to VS and highly correlated to hypoxia, another one exclusively to CBV showing strong enrichments in the Epithelial Growth Factor (EGF) pathway and Epithelial-to-Mesenchymal-Transition (EMT). Moreover, patients with increased CBV and VS predominantly showed a mesenchymal gene-expression, a finding that could be corroborated by TCGA data. In conclusion, CBV and VS mirror different genetic pathways and reflect certain molecular subclasses of GBM. Impact Journals LLC 2016-08-23 /pmc/articles/PMC5355248/ /pubmed/27613830 http://dx.doi.org/10.18632/oncotarget.11522 Text en Copyright: © 2017 Heiland et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Heiland, Dieter Henrik
Demerath, Theo
Kellner, Elias
Kiselev, Valerij G.
Pfeifer, Dietmar
Schnell, Oliver
Staszewski, Ori
Urbach, Horst
Weyerbrock, Astrid
Mader, Irina
Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme
title Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme
title_full Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme
title_fullStr Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme
title_full_unstemmed Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme
title_short Molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme
title_sort molecular differences between cerebral blood volume and vessel size in glioblastoma multiforme
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355248/
https://www.ncbi.nlm.nih.gov/pubmed/27613830
http://dx.doi.org/10.18632/oncotarget.11522
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