A cross-study gene set enrichment analysis identifies critical pathways in endometriosis

<p>Abstract</p> <p>Background</p> <p>Endometriosis is an enigmatic disease. Gene expression profiling of endometriosis has been used in several studies, but few studies went further to classify subtypes of endometriosis based on expression patterns and to identify possi...

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Main Authors: Bai Chunyan, Wang Qishan, Zhao Hongbo, He Kan, Pan Yuchun
Format: Article
Language:English
Published: BMC 2009-09-01
Series:Reproductive Biology and Endocrinology
Online Access:http://www.rbej.com/content/7/1/94
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spelling doaj-baa9be36303c4b63977cc65b51e620a62020-11-24T21:59:43ZengBMCReproductive Biology and Endocrinology1477-78272009-09-01719410.1186/1477-7827-7-94A cross-study gene set enrichment analysis identifies critical pathways in endometriosisBai ChunyanWang QishanZhao HongboHe KanPan Yuchun<p>Abstract</p> <p>Background</p> <p>Endometriosis is an enigmatic disease. Gene expression profiling of endometriosis has been used in several studies, but few studies went further to classify subtypes of endometriosis based on expression patterns and to identify possible pathways involved in endometriosis. Some of the observed pathways are more inconsistent between the studies, and these candidate pathways presumably only represent a fraction of the pathways involved in endometriosis.</p> <p>Methods</p> <p>We applied a standardised microarray preprocessing and gene set enrichment analysis to six independent studies, and demonstrated increased concordance between these gene datasets.</p> <p>Results</p> <p>We find 16 up-regulated and 19 down-regulated pathways common in ovarian endometriosis data sets, 22 up-regulated and one down-regulated pathway common in peritoneal endometriosis data sets. Among them, 12 up-regulated and 1 down-regulated were found consistent between ovarian and peritoneal endometriosis. The main canonical pathways identified are related to immunological and inflammatory disease. Early secretory phase has the most over-represented pathways in the three uterine cycle phases. There are no overlapping significant pathways between the dataset from human endometrial endothelial cells and the datasets from ovarian endometriosis which used whole tissues.</p> <p>Conclusion</p> <p>The study of complex diseases through pathway analysis is able to highlight genes weakly connected to the phenotype which may be difficult to detect by using classical univariate statistics. By standardised microarray preprocessing and GSEA, we have increased the concordance in identifying many biological mechanisms involved in endometriosis. The identified gene pathways will shed light on the understanding of endometriosis and promote the development of novel therapies.</p> http://www.rbej.com/content/7/1/94
collection DOAJ
language English
format Article
sources DOAJ
author Bai Chunyan
Wang Qishan
Zhao Hongbo
He Kan
Pan Yuchun
spellingShingle Bai Chunyan
Wang Qishan
Zhao Hongbo
He Kan
Pan Yuchun
A cross-study gene set enrichment analysis identifies critical pathways in endometriosis
Reproductive Biology and Endocrinology
author_facet Bai Chunyan
Wang Qishan
Zhao Hongbo
He Kan
Pan Yuchun
author_sort Bai Chunyan
title A cross-study gene set enrichment analysis identifies critical pathways in endometriosis
title_short A cross-study gene set enrichment analysis identifies critical pathways in endometriosis
title_full A cross-study gene set enrichment analysis identifies critical pathways in endometriosis
title_fullStr A cross-study gene set enrichment analysis identifies critical pathways in endometriosis
title_full_unstemmed A cross-study gene set enrichment analysis identifies critical pathways in endometriosis
title_sort cross-study gene set enrichment analysis identifies critical pathways in endometriosis
publisher BMC
series Reproductive Biology and Endocrinology
issn 1477-7827
publishDate 2009-09-01
description <p>Abstract</p> <p>Background</p> <p>Endometriosis is an enigmatic disease. Gene expression profiling of endometriosis has been used in several studies, but few studies went further to classify subtypes of endometriosis based on expression patterns and to identify possible pathways involved in endometriosis. Some of the observed pathways are more inconsistent between the studies, and these candidate pathways presumably only represent a fraction of the pathways involved in endometriosis.</p> <p>Methods</p> <p>We applied a standardised microarray preprocessing and gene set enrichment analysis to six independent studies, and demonstrated increased concordance between these gene datasets.</p> <p>Results</p> <p>We find 16 up-regulated and 19 down-regulated pathways common in ovarian endometriosis data sets, 22 up-regulated and one down-regulated pathway common in peritoneal endometriosis data sets. Among them, 12 up-regulated and 1 down-regulated were found consistent between ovarian and peritoneal endometriosis. The main canonical pathways identified are related to immunological and inflammatory disease. Early secretory phase has the most over-represented pathways in the three uterine cycle phases. There are no overlapping significant pathways between the dataset from human endometrial endothelial cells and the datasets from ovarian endometriosis which used whole tissues.</p> <p>Conclusion</p> <p>The study of complex diseases through pathway analysis is able to highlight genes weakly connected to the phenotype which may be difficult to detect by using classical univariate statistics. By standardised microarray preprocessing and GSEA, we have increased the concordance in identifying many biological mechanisms involved in endometriosis. The identified gene pathways will shed light on the understanding of endometriosis and promote the development of novel therapies.</p>
url http://www.rbej.com/content/7/1/94
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