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DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays
We report a method, Expression-Microarray Copy Number Analysis (ECNA) for the detection of copy number changes using Affymetrix Human Genome U133 Plus 2.0 arrays, starting with as little as 5 ng input genomic DNA. An analytical approach was developed using DNA isolated from cell lines containing var...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Libertas Academica
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2623304/ https://www.ncbi.nlm.nih.gov/pubmed/19259404 |
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author | Antonescu, Cristina R. Wu, Kai Xing, Guoliang Leon Cao, Manqiu Turpaz, Yaron Leversha, Margaret A. Hubbell, Earl Maki, Robert G. Miyada, C. Garrett Pillai, Raji |
author_facet | Antonescu, Cristina R. Wu, Kai Xing, Guoliang Leon Cao, Manqiu Turpaz, Yaron Leversha, Margaret A. Hubbell, Earl Maki, Robert G. Miyada, C. Garrett Pillai, Raji |
author_sort | Antonescu, Cristina R. |
collection | PubMed |
description | We report a method, Expression-Microarray Copy Number Analysis (ECNA) for the detection of copy number changes using Affymetrix Human Genome U133 Plus 2.0 arrays, starting with as little as 5 ng input genomic DNA. An analytical approach was developed using DNA isolated from cell lines containing various X-chromosome numbers, and validated with DNA from cell lines with defined deletions and amplifications in other chromosomal locations. We applied this method to examine the copy number changes in DNA from 5 frozen gastrointestinal stromal tumors (GIST). We detected known copy number aberrations consistent with previously published results using conventional or BAC-array CGH, as well as novel changes in GIST tumors. These changes were concordant with results from Affymetrix 100K human SNP mapping arrays. Gene expression data for these GIST samples had previously been generated on U133A arrays, allowing us to explore correlations between chromosomal copy number and RNA expression levels. One of the novel aberrations identified in the GIST samples, a previously unreported gain on 1q21.1 containing the PEX11B gene, was confirmed in this study by FISH and was also shown to have significant differences in expression pattern when compared to a control sample. In summary, we have demonstrated the use of gene expression microarrays for the detection of genomic copy number aberrations in tumor samples. This method may be used to study copy number changes in other species for which RNA expression arrays are available, e.g. other mammals, plants, etc., and for which SNPs have not yet been mapped. |
format | Text |
id | pubmed-2623304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-26233042009-02-24 DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays Antonescu, Cristina R. Wu, Kai Xing, Guoliang Leon Cao, Manqiu Turpaz, Yaron Leversha, Margaret A. Hubbell, Earl Maki, Robert G. Miyada, C. Garrett Pillai, Raji Cancer Inform Original Research We report a method, Expression-Microarray Copy Number Analysis (ECNA) for the detection of copy number changes using Affymetrix Human Genome U133 Plus 2.0 arrays, starting with as little as 5 ng input genomic DNA. An analytical approach was developed using DNA isolated from cell lines containing various X-chromosome numbers, and validated with DNA from cell lines with defined deletions and amplifications in other chromosomal locations. We applied this method to examine the copy number changes in DNA from 5 frozen gastrointestinal stromal tumors (GIST). We detected known copy number aberrations consistent with previously published results using conventional or BAC-array CGH, as well as novel changes in GIST tumors. These changes were concordant with results from Affymetrix 100K human SNP mapping arrays. Gene expression data for these GIST samples had previously been generated on U133A arrays, allowing us to explore correlations between chromosomal copy number and RNA expression levels. One of the novel aberrations identified in the GIST samples, a previously unreported gain on 1q21.1 containing the PEX11B gene, was confirmed in this study by FISH and was also shown to have significant differences in expression pattern when compared to a control sample. In summary, we have demonstrated the use of gene expression microarrays for the detection of genomic copy number aberrations in tumor samples. This method may be used to study copy number changes in other species for which RNA expression arrays are available, e.g. other mammals, plants, etc., and for which SNPs have not yet been mapped. Libertas Academica 2008-03-27 /pmc/articles/PMC2623304/ /pubmed/19259404 Text en © 2008 by the authors http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Original Research Antonescu, Cristina R. Wu, Kai Xing, Guoliang Leon Cao, Manqiu Turpaz, Yaron Leversha, Margaret A. Hubbell, Earl Maki, Robert G. Miyada, C. Garrett Pillai, Raji DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays |
title | DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays |
title_full | DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays |
title_fullStr | DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays |
title_full_unstemmed | DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays |
title_short | DNA Copy Number Analysis in Gastrointestinal Stromal Tumors Using Gene Expression Microarrays |
title_sort | dna copy number analysis in gastrointestinal stromal tumors using gene expression microarrays |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2623304/ https://www.ncbi.nlm.nih.gov/pubmed/19259404 |
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