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Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers

BACKGROUND: Although prognostic biomarkers specific for particular cancers have been discovered, microarray analysis of gene expression profiles, supported by integrative analysis algorithms, helps to identify common factors in molecular oncology. Similarities of Ordered Gene Lists (SOGL) is a recen...

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Detalles Bibliográficos
Autores principales: Yang, Xinan, Sun, Xiao
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1853113/
https://www.ncbi.nlm.nih.gov/pubmed/17411443
http://dx.doi.org/10.1186/1471-2105-8-118
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author Yang, Xinan
Sun, Xiao
author_facet Yang, Xinan
Sun, Xiao
author_sort Yang, Xinan
collection PubMed
description BACKGROUND: Although prognostic biomarkers specific for particular cancers have been discovered, microarray analysis of gene expression profiles, supported by integrative analysis algorithms, helps to identify common factors in molecular oncology. Similarities of Ordered Gene Lists (SOGL) is a recently proposed approach to meta-analysis suitable for identifying features shared by two data sets. Here we extend the idea of SOGL to the detection of significant prognostic marker genes from microarrays of multiple data sets. Three data sets for leukemia and the other six for different solid tumors are used to demonstrate our method, using established statistical techniques. RESULTS: We describe a set of significantly similar ordered gene lists, representing outcome comparisons for distinct types of cancer. This kind of similarity could improve the diagnostic accuracies of individual studies when SOGL is incorporated into the support vector machine algorithm. In particular, we investigate the similarities among three ordered gene lists pertaining to mesothelioma survival, prostate recurrence and glioma survival. The similarity-driving genes are related to the outcomes of patients with lung cancer with a hazard ratio of 4.47 (p = 0.035). Many of these genes are involved in breakdown of EMC proteins regulating angiogenesis, and may be used for further research on prognostic markers and molecular targets of gene therapy for cancers. CONCLUSION: The proposed method and its application show the potential of such meta-analyses in clinical studies of gene expression profiles.
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spelling pubmed-18531132007-04-20 Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers Yang, Xinan Sun, Xiao BMC Bioinformatics Research Article BACKGROUND: Although prognostic biomarkers specific for particular cancers have been discovered, microarray analysis of gene expression profiles, supported by integrative analysis algorithms, helps to identify common factors in molecular oncology. Similarities of Ordered Gene Lists (SOGL) is a recently proposed approach to meta-analysis suitable for identifying features shared by two data sets. Here we extend the idea of SOGL to the detection of significant prognostic marker genes from microarrays of multiple data sets. Three data sets for leukemia and the other six for different solid tumors are used to demonstrate our method, using established statistical techniques. RESULTS: We describe a set of significantly similar ordered gene lists, representing outcome comparisons for distinct types of cancer. This kind of similarity could improve the diagnostic accuracies of individual studies when SOGL is incorporated into the support vector machine algorithm. In particular, we investigate the similarities among three ordered gene lists pertaining to mesothelioma survival, prostate recurrence and glioma survival. The similarity-driving genes are related to the outcomes of patients with lung cancer with a hazard ratio of 4.47 (p = 0.035). Many of these genes are involved in breakdown of EMC proteins regulating angiogenesis, and may be used for further research on prognostic markers and molecular targets of gene therapy for cancers. CONCLUSION: The proposed method and its application show the potential of such meta-analyses in clinical studies of gene expression profiles. BioMed Central 2007-04-06 /pmc/articles/PMC1853113/ /pubmed/17411443 http://dx.doi.org/10.1186/1471-2105-8-118 Text en Copyright © 2007 Yang and Sun; 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
Yang, Xinan
Sun, Xiao
Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers
title Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers
title_full Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers
title_fullStr Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers
title_full_unstemmed Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers
title_short Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers
title_sort meta-analysis of several gene lists for distinct types of cancer: a simple way to reveal common prognostic markers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1853113/
https://www.ncbi.nlm.nih.gov/pubmed/17411443
http://dx.doi.org/10.1186/1471-2105-8-118
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