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Gene Expression in Oligodendroglial Tumors

Background: Oligodendroglial tumors with 1p/19q loss are more likely to be chemosensitive and have longer survival than those with intact 1p/19q, but not all respond to chemotherapy, warranting investigation of the biological basis of chemosensitivity. Methods: Gene expression profiling was performe...

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Autores principales: Shaw, Elisabeth J., Haylock, Brian, Husband, David, du Plessis, Daniel, Sibson, D. Ross, Warnke, Peter C., Walker, Carol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605574/
https://www.ncbi.nlm.nih.gov/pubmed/20966545
http://dx.doi.org/10.3233/ACP-CLO-2010-0533
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author Shaw, Elisabeth J.
Haylock, Brian
Husband, David
du Plessis, Daniel
Sibson, D. Ross
Warnke, Peter C.
Walker, Carol
author_facet Shaw, Elisabeth J.
Haylock, Brian
Husband, David
du Plessis, Daniel
Sibson, D. Ross
Warnke, Peter C.
Walker, Carol
author_sort Shaw, Elisabeth J.
collection PubMed
description Background: Oligodendroglial tumors with 1p/19q loss are more likely to be chemosensitive and have longer survival than those with intact 1p/19q, but not all respond to chemotherapy, warranting investigation of the biological basis of chemosensitivity. Methods: Gene expression profiling was performed using amplified antisense RNA from 28 oligodendroglial tumors treated with chemotherapy (26 serial stereotactic biopsy, 2 resection). Expression of differentially expressed genes was validated by real-time PCR. Results: Unsupervised hierarchical clustering showed clustering of multiple samples from the same case in 14/17 cases and identified subgroups associated with tumor grade and 1p/19q status. 176 genes were differentially expressed, 164 being associated with 1p/19q loss (86% not on 1p or 19q). 94 genes differed between responders and non-responders to chemotherapy; 12 were not associated with 1p/19q loss. Significant differential expression was confirmed in 11/13 selected genes. Novel genes associated with response to therapy included SSBP2, GFRA1, FAP and RASD1. IQGAP1, INA, TGIF1, NR2F2 and MYCBP were differentially expressed in oligodendroglial tumors with 1p/19q loss. Conclusion: Gene expression profiling using serial stereotactic biopsies indicated greater homogeneity within tumors than between tumors. Genes associated with 1p/19q status or response were identified warranting further elucidation of their role in oligodendroglial tumors.
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spelling pubmed-46055742015-12-13 Gene Expression in Oligodendroglial Tumors Shaw, Elisabeth J. Haylock, Brian Husband, David du Plessis, Daniel Sibson, D. Ross Warnke, Peter C. Walker, Carol Anal Cell Pathol (Amst) Other Background: Oligodendroglial tumors with 1p/19q loss are more likely to be chemosensitive and have longer survival than those with intact 1p/19q, but not all respond to chemotherapy, warranting investigation of the biological basis of chemosensitivity. Methods: Gene expression profiling was performed using amplified antisense RNA from 28 oligodendroglial tumors treated with chemotherapy (26 serial stereotactic biopsy, 2 resection). Expression of differentially expressed genes was validated by real-time PCR. Results: Unsupervised hierarchical clustering showed clustering of multiple samples from the same case in 14/17 cases and identified subgroups associated with tumor grade and 1p/19q status. 176 genes were differentially expressed, 164 being associated with 1p/19q loss (86% not on 1p or 19q). 94 genes differed between responders and non-responders to chemotherapy; 12 were not associated with 1p/19q loss. Significant differential expression was confirmed in 11/13 selected genes. Novel genes associated with response to therapy included SSBP2, GFRA1, FAP and RASD1. IQGAP1, INA, TGIF1, NR2F2 and MYCBP were differentially expressed in oligodendroglial tumors with 1p/19q loss. Conclusion: Gene expression profiling using serial stereotactic biopsies indicated greater homogeneity within tumors than between tumors. Genes associated with 1p/19q status or response were identified warranting further elucidation of their role in oligodendroglial tumors. IOS Press 2010 2010-07-15 /pmc/articles/PMC4605574/ /pubmed/20966545 http://dx.doi.org/10.3233/ACP-CLO-2010-0533 Text en Copyright © 2010 Hindawi Publishing Corporation and the authors.
spellingShingle Other
Shaw, Elisabeth J.
Haylock, Brian
Husband, David
du Plessis, Daniel
Sibson, D. Ross
Warnke, Peter C.
Walker, Carol
Gene Expression in Oligodendroglial Tumors
title Gene Expression in Oligodendroglial Tumors
title_full Gene Expression in Oligodendroglial Tumors
title_fullStr Gene Expression in Oligodendroglial Tumors
title_full_unstemmed Gene Expression in Oligodendroglial Tumors
title_short Gene Expression in Oligodendroglial Tumors
title_sort gene expression in oligodendroglial tumors
topic Other
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605574/
https://www.ncbi.nlm.nih.gov/pubmed/20966545
http://dx.doi.org/10.3233/ACP-CLO-2010-0533
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