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The proteomic response in glioblastoma in young patients

Increasing age is an important prognostic variable in glioblastoma (GBM). We have defined the proteomic response in GBM samples from 7 young patients (mean age 36 years) compared to peritumoural-control samples from 10 young patients (mean age 32 years). 2-Dimensional-gel-electrophoresis, image anal...

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Autores principales: Deighton, Ruth F., Le Bihan, Thierry, Martin, Sarah F., Barrios-Llerena, Martin E., Gerth, Alice M. J., Kerr, Lorraine E., McCulloch, James, Whittle, Ian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129242/
https://www.ncbi.nlm.nih.gov/pubmed/24838487
http://dx.doi.org/10.1007/s11060-014-1474-6
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author Deighton, Ruth F.
Le Bihan, Thierry
Martin, Sarah F.
Barrios-Llerena, Martin E.
Gerth, Alice M. J.
Kerr, Lorraine E.
McCulloch, James
Whittle, Ian R.
author_facet Deighton, Ruth F.
Le Bihan, Thierry
Martin, Sarah F.
Barrios-Llerena, Martin E.
Gerth, Alice M. J.
Kerr, Lorraine E.
McCulloch, James
Whittle, Ian R.
author_sort Deighton, Ruth F.
collection PubMed
description Increasing age is an important prognostic variable in glioblastoma (GBM). We have defined the proteomic response in GBM samples from 7 young patients (mean age 36 years) compared to peritumoural-control samples from 10 young patients (mean age 32 years). 2-Dimensional-gel-electrophoresis, image analysis, and protein identification (LC/MS) were performed. 68 proteins were significantly altered in young GBM samples with 29 proteins upregulated and 39 proteins downregulated. Over 50 proteins are described as altered in GBM for the first time. In a parallel analysis in old GBM (mean age 67 years), an excellent correlation could be demonstrated between the proteomic profile in young GBM and that in old GBM patients (r(2) = 0.95) with only 5 proteins altered significantly (p < 0.01). The proteomic response in young GBM patients highlighted alterations in protein–protein interactions in the immunoproteosome, NFkB signalling, and mitochondrial function and the same systems participated in the responses in old GBM patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11060-014-1474-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-41292422014-08-21 The proteomic response in glioblastoma in young patients Deighton, Ruth F. Le Bihan, Thierry Martin, Sarah F. Barrios-Llerena, Martin E. Gerth, Alice M. J. Kerr, Lorraine E. McCulloch, James Whittle, Ian R. J Neurooncol Laboratory Investigation Increasing age is an important prognostic variable in glioblastoma (GBM). We have defined the proteomic response in GBM samples from 7 young patients (mean age 36 years) compared to peritumoural-control samples from 10 young patients (mean age 32 years). 2-Dimensional-gel-electrophoresis, image analysis, and protein identification (LC/MS) were performed. 68 proteins were significantly altered in young GBM samples with 29 proteins upregulated and 39 proteins downregulated. Over 50 proteins are described as altered in GBM for the first time. In a parallel analysis in old GBM (mean age 67 years), an excellent correlation could be demonstrated between the proteomic profile in young GBM and that in old GBM patients (r(2) = 0.95) with only 5 proteins altered significantly (p < 0.01). The proteomic response in young GBM patients highlighted alterations in protein–protein interactions in the immunoproteosome, NFkB signalling, and mitochondrial function and the same systems participated in the responses in old GBM patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11060-014-1474-6) contains supplementary material, which is available to authorized users. Springer US 2014-05-18 2014 /pmc/articles/PMC4129242/ /pubmed/24838487 http://dx.doi.org/10.1007/s11060-014-1474-6 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Laboratory Investigation
Deighton, Ruth F.
Le Bihan, Thierry
Martin, Sarah F.
Barrios-Llerena, Martin E.
Gerth, Alice M. J.
Kerr, Lorraine E.
McCulloch, James
Whittle, Ian R.
The proteomic response in glioblastoma in young patients
title The proteomic response in glioblastoma in young patients
title_full The proteomic response in glioblastoma in young patients
title_fullStr The proteomic response in glioblastoma in young patients
title_full_unstemmed The proteomic response in glioblastoma in young patients
title_short The proteomic response in glioblastoma in young patients
title_sort proteomic response in glioblastoma in young patients
topic Laboratory Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4129242/
https://www.ncbi.nlm.nih.gov/pubmed/24838487
http://dx.doi.org/10.1007/s11060-014-1474-6
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