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Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer
Alternative processing of pre-mRNA transcripts is a major source of protein diversity in eukaryotes and has been implicated in several disease processes including cancer. In this study we have performed a genome wide analysis of alternative splicing events in lung adenocarcinoma. We found that 2369...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582617/ https://www.ncbi.nlm.nih.gov/pubmed/18927117 http://dx.doi.org/10.1093/nar/gkn697 |
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author | Xi, Liqiang Feber, Andrew Gupta, Vanita Wu, Maoxin Bergemann, Andrew D. Landreneau, Rodney J. Litle, Virginia R. Pennathur, Arjun Luketich, James D. Godfrey, Tony E. |
author_facet | Xi, Liqiang Feber, Andrew Gupta, Vanita Wu, Maoxin Bergemann, Andrew D. Landreneau, Rodney J. Litle, Virginia R. Pennathur, Arjun Luketich, James D. Godfrey, Tony E. |
author_sort | Xi, Liqiang |
collection | PubMed |
description | Alternative processing of pre-mRNA transcripts is a major source of protein diversity in eukaryotes and has been implicated in several disease processes including cancer. In this study we have performed a genome wide analysis of alternative splicing events in lung adenocarcinoma. We found that 2369 of the 17 800 core Refseq genes appear to have alternative transcripts that are differentially expressed in lung adenocarcinoma versus normal. According to their known functions the largest subset of these genes (30.8%) is believed to be cancer related. Detailed analysis was performed for several genes using PCR, quantitative RT-PCR and DNA sequencing. We found overexpression of ERG variant 2 but not variant 1 in lung tumors and overexpression of CEACAM1 variant 1 but not variant 2 in lung tumors but not in breast or colon tumors. We also identified a novel, overexpressed variant of CDH3 and verified the existence and overexpression of a novel variant of P16 transcribed from the CDKN2A locus. These findings demonstrate how analysis of alternative pre-mRNA processing can shed additional light on differences between tumors and normal tissues as well as between different tumor types. Such studies may lead to the development of additional tools for tumor diagnosis, prognosis and therapy. |
format | Text |
id | pubmed-2582617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-25826172009-01-22 Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer Xi, Liqiang Feber, Andrew Gupta, Vanita Wu, Maoxin Bergemann, Andrew D. Landreneau, Rodney J. Litle, Virginia R. Pennathur, Arjun Luketich, James D. Godfrey, Tony E. Nucleic Acids Res Genomics Alternative processing of pre-mRNA transcripts is a major source of protein diversity in eukaryotes and has been implicated in several disease processes including cancer. In this study we have performed a genome wide analysis of alternative splicing events in lung adenocarcinoma. We found that 2369 of the 17 800 core Refseq genes appear to have alternative transcripts that are differentially expressed in lung adenocarcinoma versus normal. According to their known functions the largest subset of these genes (30.8%) is believed to be cancer related. Detailed analysis was performed for several genes using PCR, quantitative RT-PCR and DNA sequencing. We found overexpression of ERG variant 2 but not variant 1 in lung tumors and overexpression of CEACAM1 variant 1 but not variant 2 in lung tumors but not in breast or colon tumors. We also identified a novel, overexpressed variant of CDH3 and verified the existence and overexpression of a novel variant of P16 transcribed from the CDKN2A locus. These findings demonstrate how analysis of alternative pre-mRNA processing can shed additional light on differences between tumors and normal tissues as well as between different tumor types. Such studies may lead to the development of additional tools for tumor diagnosis, prognosis and therapy. Oxford University Press 2008-11 2008-10-16 /pmc/articles/PMC2582617/ /pubmed/18927117 http://dx.doi.org/10.1093/nar/gkn697 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genomics Xi, Liqiang Feber, Andrew Gupta, Vanita Wu, Maoxin Bergemann, Andrew D. Landreneau, Rodney J. Litle, Virginia R. Pennathur, Arjun Luketich, James D. Godfrey, Tony E. Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer |
title | Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer |
title_full | Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer |
title_fullStr | Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer |
title_full_unstemmed | Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer |
title_short | Whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer |
title_sort | whole genome exon arrays identify differential expression of alternatively spliced, cancer-related genes in lung cancer |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582617/ https://www.ncbi.nlm.nih.gov/pubmed/18927117 http://dx.doi.org/10.1093/nar/gkn697 |
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