Analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus

Abstract Background This study was aimed at screening out the potential key genes and pathways associated with gestational diabetes mellitus (GDM). Methods The GSE70493 dataset used for this study was obtained from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) in the pl...

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Main Authors: Yuxia Wang, Haifeng Yu, Fangmei Liu, Xiue Song
Format: Article
Language:English
Published: BMC 2019-11-01
Series:Reproductive Biology and Endocrinology
Subjects:
Online Access:https://doi.org/10.1186/s12958-019-0546-z
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author Yuxia Wang
Haifeng Yu
Fangmei Liu
Xiue Song
author_facet Yuxia Wang
Haifeng Yu
Fangmei Liu
Xiue Song
author_sort Yuxia Wang
collection DOAJ
description Abstract Background This study was aimed at screening out the potential key genes and pathways associated with gestational diabetes mellitus (GDM). Methods The GSE70493 dataset used for this study was obtained from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) in the placental tissue of women with GDM in relation to the control tissue samples were identified and submitted to protein-protein interaction (PPI) network analysis and subnetwork module mining. Functional enrichment analyses of the PPI network and subnetworks were subsequently carried out. Finally, the integrated miRNA–transcription factor (TF)–DEG regulatory network was analyzed. Results In total, 238 DEGs were identified, of which 162 were upregulated and 76 were downregulated. Through PPI network construction, 108 nodes and 278 gene pairs were obtained, from which chemokine (C-X-C motif) ligand 9 (CXCL9), CXCL10, protein tyrosine phosphatase, receptor type C (PTPRC), and human leukocyte antigen (HLA) were screened out as hub genes. Moreover, genes associated with the immune-related pathway and immune responses were found to be significantly enriched in the process of GDM. Finally, miRNAs and TFs that target the DEGs were predicted. Conclusions Four candidate genes (viz., CXCL9, CXCL10, PTPRC, and HLA) are closely related to GDM. miR-223-3p, miR-520, and thioredoxin-binding protein may play important roles in the pathogenesis of this disease.
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spelling doaj.art-84db46e621d2456f8a539972d04303922022-12-21T23:44:28ZengBMCReproductive Biology and Endocrinology1477-78272019-11-0117111010.1186/s12958-019-0546-zAnalysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitusYuxia Wang0Haifeng Yu1Fangmei Liu2Xiue Song3Department of Gynecology, Jinan Central HospitalDepartment of Obstetrics, Jinan Central HospitalDepartment of Obstetrics, Jinan Central HospitalDepartment of Obstetrics, Jinan Central HospitalAbstract Background This study was aimed at screening out the potential key genes and pathways associated with gestational diabetes mellitus (GDM). Methods The GSE70493 dataset used for this study was obtained from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) in the placental tissue of women with GDM in relation to the control tissue samples were identified and submitted to protein-protein interaction (PPI) network analysis and subnetwork module mining. Functional enrichment analyses of the PPI network and subnetworks were subsequently carried out. Finally, the integrated miRNA–transcription factor (TF)–DEG regulatory network was analyzed. Results In total, 238 DEGs were identified, of which 162 were upregulated and 76 were downregulated. Through PPI network construction, 108 nodes and 278 gene pairs were obtained, from which chemokine (C-X-C motif) ligand 9 (CXCL9), CXCL10, protein tyrosine phosphatase, receptor type C (PTPRC), and human leukocyte antigen (HLA) were screened out as hub genes. Moreover, genes associated with the immune-related pathway and immune responses were found to be significantly enriched in the process of GDM. Finally, miRNAs and TFs that target the DEGs were predicted. Conclusions Four candidate genes (viz., CXCL9, CXCL10, PTPRC, and HLA) are closely related to GDM. miR-223-3p, miR-520, and thioredoxin-binding protein may play important roles in the pathogenesis of this disease.https://doi.org/10.1186/s12958-019-0546-zGestational diabetes mellitusDifferentially expressed genesProtein-protein interaction networkIntegrated regulatory networkTranscription factors
spellingShingle Yuxia Wang
Haifeng Yu
Fangmei Liu
Xiue Song
Analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus
Reproductive Biology and Endocrinology
Gestational diabetes mellitus
Differentially expressed genes
Protein-protein interaction network
Integrated regulatory network
Transcription factors
title Analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus
title_full Analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus
title_fullStr Analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus
title_full_unstemmed Analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus
title_short Analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus
title_sort analysis of key genes and their functions in placental tissue of patients with gestational diabetes mellitus
topic Gestational diabetes mellitus
Differentially expressed genes
Protein-protein interaction network
Integrated regulatory network
Transcription factors
url https://doi.org/10.1186/s12958-019-0546-z
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