Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO Databases

Purpose. To identify novel biomarkers of IgA nephropathy (IgAN) through bioinformatics analysis and elucidate the possible molecular mechanism. Methods. The GSE93798 and GSE73953 datasets containing microarray data from IgAN patients and healthy controls were downloaded from the GEO database and ana...

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Main Authors: Wang Qian, Wang Xiaoyi, Ye Zi
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2019/8794013
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spelling doaj-d4dd5d8ffda64d578ff118a939556f4a2020-11-24T22:12:26ZengHindawi LimitedBioMed Research International2314-61332314-61412019-01-01201910.1155/2019/87940138794013Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO DatabasesWang Qian0Wang Xiaoyi1Ye Zi2Department of Nephrology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaDepartment of Gastroenterology, Shanghai Traditional Chinese Medicine-Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaDepartment of Nephrology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, ChinaPurpose. To identify novel biomarkers of IgA nephropathy (IgAN) through bioinformatics analysis and elucidate the possible molecular mechanism. Methods. The GSE93798 and GSE73953 datasets containing microarray data from IgAN patients and healthy controls were downloaded from the GEO database and analyzed by the GEO2R web tool to obtain different expressed genes (DEGs). Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis, protein-protein interaction (PPI), and Biological Networks Gene Oncology tool (BiNGO) were then performed to elucidate the molecular mechanism of IgAN. Results. A total of 223 DEGs were identified, of which 21 were hub genes, and involved in inflammatory response, cellular response to lipopolysaccharide, transcription factor activity, extracellular exosome, TNF signaling pathway, and MAPK signaling pathway. Conclusions. TNF and MAPK pathways likely form the basis of IgAN progression, and JUN/JUNB, FOS, NR4A1/2, EGR1, and FOSL1/2 are novel prognostic biomarkers of IgAN.http://dx.doi.org/10.1155/2019/8794013
collection DOAJ
language English
format Article
sources DOAJ
author Wang Qian
Wang Xiaoyi
Ye Zi
spellingShingle Wang Qian
Wang Xiaoyi
Ye Zi
Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO Databases
BioMed Research International
author_facet Wang Qian
Wang Xiaoyi
Ye Zi
author_sort Wang Qian
title Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO Databases
title_short Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO Databases
title_full Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO Databases
title_fullStr Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO Databases
title_full_unstemmed Screening and Bioinformatics Analysis of IgA Nephropathy Gene Based on GEO Databases
title_sort screening and bioinformatics analysis of iga nephropathy gene based on geo databases
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2019-01-01
description Purpose. To identify novel biomarkers of IgA nephropathy (IgAN) through bioinformatics analysis and elucidate the possible molecular mechanism. Methods. The GSE93798 and GSE73953 datasets containing microarray data from IgAN patients and healthy controls were downloaded from the GEO database and analyzed by the GEO2R web tool to obtain different expressed genes (DEGs). Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis, protein-protein interaction (PPI), and Biological Networks Gene Oncology tool (BiNGO) were then performed to elucidate the molecular mechanism of IgAN. Results. A total of 223 DEGs were identified, of which 21 were hub genes, and involved in inflammatory response, cellular response to lipopolysaccharide, transcription factor activity, extracellular exosome, TNF signaling pathway, and MAPK signaling pathway. Conclusions. TNF and MAPK pathways likely form the basis of IgAN progression, and JUN/JUNB, FOS, NR4A1/2, EGR1, and FOSL1/2 are novel prognostic biomarkers of IgAN.
url http://dx.doi.org/10.1155/2019/8794013
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AT wangxiaoyi screeningandbioinformaticsanalysisofiganephropathygenebasedongeodatabases
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