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Multiple outcome meta-analysis of gene-expression data in inflammatory bowel disease

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Autore
Vennou K.E., Piovani D., Kontou P.I., Bonovas S., Bagos P.G.
Data
2020
Language
en
DOI
10.1016/j.ygeno.2019.09.019
Soggetto
apoptosis
Article
BCAT1 gene
carcinogenesis
cell adhesion
Crohn disease
gene
gene expression
gene function
gene identification
genetic analysis
genetic variability
GZMB gene
human
interferon gamma signaling
JAK-STAT signaling
microarray analysis
outcome assessment
pathogenesis
priority journal
signal transduction
ulcerative colitis
Crohn disease
genetics
meta analysis
metabolism
ulcerative colitis
aminotransferase
BCAT1 protein, human
gamma interferon
granzyme
GZMB protein, human
Janus kinase
STAT protein
transcriptome
Colitis, Ulcerative
Crohn Disease
Granzymes
Humans
Interferon-gamma
Janus Kinases
Signal Transduction
STAT Transcription Factors
Transaminases
Transcriptome
Academic Press Inc.
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Abstract
We performed a multivariate meta-analysis of microarray data in Crohn's disease (CD) and Ulcerative colitis (UC), which are the main forms of inflammatory bowel disease (IBD). They share similar symptoms but differ in the location and extent of inflammation and in complications. We identified 249 differentially expressed genes (DEGs) in CD and 38 in UC at a false discovery rate of 1%. 20 of the DEGs were common to both diseases. A multivariate test identified 260 DEGs associated with IBD, 53 of which were not found in any of the disorders. We identified important molecular pathways implicated in the pathogenesis of IBD, such as the JAK/STAT and interferon-gamma signaling pathways, genes involved in cell adhesion, apoptosis and carcinogenesis. Among others, BCAT1 and GZMB are interesting novel DEGs that deserve further investigation in experimental models. The method could also be useful to other cases of meta-analysis of gene expression data. © 2019 Elsevier Inc.
URI
http://hdl.handle.net/11615/80578
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