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RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls
BACKGROUND: RNA from exosomes and other microvesicles contain transcripts of tumour origin. In this study we sought to identify biomarkers of glioblastoma multiforme in microvesicle RNA from serum of affected patients. METHODS: Microvesicle RNA from serum from patients with de-novo primary glioblast...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329625/ https://www.ncbi.nlm.nih.gov/pubmed/22251860 http://dx.doi.org/10.1186/1471-2407-12-22 |
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author | Noerholm, Mikkel Balaj, Leonora Limperg, Tobias Salehi, Afshin Zhu, Lin Dan Hochberg, Fred H Breakefield, Xandra O Carter, Bob S Skog, Johan |
author_facet | Noerholm, Mikkel Balaj, Leonora Limperg, Tobias Salehi, Afshin Zhu, Lin Dan Hochberg, Fred H Breakefield, Xandra O Carter, Bob S Skog, Johan |
author_sort | Noerholm, Mikkel |
collection | PubMed |
description | BACKGROUND: RNA from exosomes and other microvesicles contain transcripts of tumour origin. In this study we sought to identify biomarkers of glioblastoma multiforme in microvesicle RNA from serum of affected patients. METHODS: Microvesicle RNA from serum from patients with de-novo primary glioblastoma multiforme (N = 9) and normal controls (N = 7) were analyzed by microarray analysis. Samples were collected according to protocols approved by the Institutional Review Board. Differential expressions were validated by qRT-PCR in a separate set of samples (N = 10 in both groups). RESULTS: Expression profiles of microvesicle RNA correctly separated individuals in two groups by unsupervised clustering. The most significant differences pertained to down-regulated genes (121 genes > 2-fold down) in the glioblastoma multiforme patient microvesicle RNA, validated by qRT-PCR on several genes. Overall, yields of microvesicle RNA from patients was higher than from normal controls, but the additional RNA was primarily of size < 500 nt. Gene ontology of the down-regulated genes indicated these are coding for ribosomal proteins and genes related to ribosome production. CONCLUSIONS: Serum microvesicle RNA from patients with glioblastoma multiforme has significantly down-regulated levels of RNAs coding for ribosome production, compared to normal healthy controls, but a large overabundance of RNA of unknown origin with size < 500 nt. |
format | Online Article Text |
id | pubmed-3329625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33296252012-04-20 RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls Noerholm, Mikkel Balaj, Leonora Limperg, Tobias Salehi, Afshin Zhu, Lin Dan Hochberg, Fred H Breakefield, Xandra O Carter, Bob S Skog, Johan BMC Cancer Research Article BACKGROUND: RNA from exosomes and other microvesicles contain transcripts of tumour origin. In this study we sought to identify biomarkers of glioblastoma multiforme in microvesicle RNA from serum of affected patients. METHODS: Microvesicle RNA from serum from patients with de-novo primary glioblastoma multiforme (N = 9) and normal controls (N = 7) were analyzed by microarray analysis. Samples were collected according to protocols approved by the Institutional Review Board. Differential expressions were validated by qRT-PCR in a separate set of samples (N = 10 in both groups). RESULTS: Expression profiles of microvesicle RNA correctly separated individuals in two groups by unsupervised clustering. The most significant differences pertained to down-regulated genes (121 genes > 2-fold down) in the glioblastoma multiforme patient microvesicle RNA, validated by qRT-PCR on several genes. Overall, yields of microvesicle RNA from patients was higher than from normal controls, but the additional RNA was primarily of size < 500 nt. Gene ontology of the down-regulated genes indicated these are coding for ribosomal proteins and genes related to ribosome production. CONCLUSIONS: Serum microvesicle RNA from patients with glioblastoma multiforme has significantly down-regulated levels of RNAs coding for ribosome production, compared to normal healthy controls, but a large overabundance of RNA of unknown origin with size < 500 nt. BioMed Central 2012-01-17 /pmc/articles/PMC3329625/ /pubmed/22251860 http://dx.doi.org/10.1186/1471-2407-12-22 Text en Copyright ©2012 Noerholm et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Noerholm, Mikkel Balaj, Leonora Limperg, Tobias Salehi, Afshin Zhu, Lin Dan Hochberg, Fred H Breakefield, Xandra O Carter, Bob S Skog, Johan RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls |
title | RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls |
title_full | RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls |
title_fullStr | RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls |
title_full_unstemmed | RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls |
title_short | RNA expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls |
title_sort | rna expression patterns in serum microvesicles from patients with glioblastoma multiforme and controls |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329625/ https://www.ncbi.nlm.nih.gov/pubmed/22251860 http://dx.doi.org/10.1186/1471-2407-12-22 |
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