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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...

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Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
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.
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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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