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pmid:31853298
Identification of differentially expressed genes and signaling pathways involved in endometriosis by integrated bioinformatics analysis.
Fang-Fang Dai · An-Yu Bao · Bing Luo · Zi-Hang Zeng · Xiao-Li Pu · Yan-Qing Wang · Li Zhang · Shu Xian · Meng-Qin Yuan · Dong-Yong Yang · Shi-Yi Liu · Yan-Xiang Cheng
Experimental and therapeutic medicine · 2020 doi:10.3892/etm.2019.8214
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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This condition causes various clinical symptoms, such as non-menstrual pelvic pain, dysmenorrhea and infertility, seriously affecting the health and quality of life of women. To date, the specific mechanism and the key molecules of endometriosis remain uncertain. The purpose of the present study was to elucidate the mechanisms involved in the development and persistence of the disease. A number of mRNA expression profile datasets (namely GSE11691, GSE23339, GSE25628 and GSE78851) were downloaded from the Gene Expression Omnibus (GEO) database. These gene expression profiles were normalized, and the differentially expressed genes (DEGs) were identified by integrated bioinformatics analysis. A total of 103 DEGs were screened upon excluding the genes that exhibited inconsistency of expression (P<0.05). Furthermore, the Gene Ontology analysis, Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis, and construction of protein-protein interaction networks of DEGs were performed using online software. The results revealed that the DEGs were closely associated with cell migration, adherens junction and hypoxia-inducible factor signaling. In addition, immunohistochemical assay results were found to be consistent with the bioinformatics results. 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