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

<p>Abstract</p> <p>Background</p> <p>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 oncolog...

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Main Authors: Sun Xiao, Yang Xinan
Format: Article
Language:English
Published: BMC 2007-04-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/8/118
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spelling doaj-2cc9168250eb4f4983eee5881c9d50d92020-11-25T01:58:21ZengBMCBMC Bioinformatics1471-21052007-04-018111810.1186/1471-2105-8-118Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markersSun XiaoYang Xinan<p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusion</p> <p>The proposed method and its application show the potential of such meta-analyses in clinical studies of gene expression profiles.</p> http://www.biomedcentral.com/1471-2105/8/118
collection DOAJ
language English
format Article
sources DOAJ
author Sun Xiao
Yang Xinan
spellingShingle Sun Xiao
Yang Xinan
Meta-analysis of several gene lists for distinct types of cancer: A simple way to reveal common prognostic markers
BMC Bioinformatics
author_facet Sun Xiao
Yang Xinan
author_sort Sun Xiao
title 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_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_sort meta-analysis of several gene lists for distinct types of cancer: a simple way to reveal common prognostic markers
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2007-04-01
description <p>Abstract</p> <p>Background</p> <p>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.</p> <p>Results</p> <p>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.</p> <p>Conclusion</p> <p>The proposed method and its application show the potential of such meta-analyses in clinical studies of gene expression profiles.</p>
url http://www.biomedcentral.com/1471-2105/8/118
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AT yangxinan metaanalysisofseveralgenelistsfordistincttypesofcancerasimplewaytorevealcommonprognosticmarkers
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