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Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis

BACKGROUND: Periodontitis is a serious health issue; however, there are few reports on periodontitis and immune related. The study sought to analyze differences in gene expression between periodontitis patients before and after treatment using bioinformatics techniques. METHODS: The GSE6751 data set...

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Autores principales: Ban, Qiang, Ling, Xiaofang, Ding, Hui, Meng, Jiansheng, Li, Yuan, Zhang, Juanfei, Zhu, Mingyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201185/
https://www.ncbi.nlm.nih.gov/pubmed/35722384
http://dx.doi.org/10.21037/atm-22-1592
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author Ban, Qiang
Ling, Xiaofang
Ding, Hui
Meng, Jiansheng
Li, Yuan
Zhang, Juanfei
Zhu, Mingyi
author_facet Ban, Qiang
Ling, Xiaofang
Ding, Hui
Meng, Jiansheng
Li, Yuan
Zhang, Juanfei
Zhu, Mingyi
author_sort Ban, Qiang
collection PubMed
description BACKGROUND: Periodontitis is a serious health issue; however, there are few reports on periodontitis and immune related. The study sought to analyze differences in gene expression between periodontitis patients before and after treatment using bioinformatics techniques. METHODS: The GSE6751 data set was screened for differentially expressed genes (DEGs) and immune-related genes using the Gene Expression Omnibus (GEO) database, a gene expression data analysis tool. Enrichment, protein-protein interaction (PPI) network construction, and immune cell correlation analyses were also performed on these genes. RESULTS: A total of 327 DEGs in periodontitis were identified, including 149 upregulated genes, 178 downregulated genes, and 27 immune-related genes. The immune-related DEGs were mainly involved in granulocyte chemotaxis, granulocyte migration, leukocyte chemotaxis, cytokine receptor binding, Toll-like receptor (TLR) binding, the phosphatidylinositol-3-kinase and protein kinase b signaling pathway, viral protein interactions with cytokines and cytokine receptors, the Ras-proximate-1 signaling pathway, the Ras signaling pathway, natural killer cell mediated cytotoxicity, and immune response related pathways. IFNG and TLR2 were the key core genes in the constructed PPI network. CONCLUSIONS: The pathogenesis of periodontitis is closely related to changes in the expression of genes, such as PF4, ANGPT1, TNFRSF1B, IFNG and TLR2, among which IFNG and TLR2 are potential therapeutic targets for periodontitis.
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spelling pubmed-92011852022-06-17 Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis Ban, Qiang Ling, Xiaofang Ding, Hui Meng, Jiansheng Li, Yuan Zhang, Juanfei Zhu, Mingyi Ann Transl Med Original Article BACKGROUND: Periodontitis is a serious health issue; however, there are few reports on periodontitis and immune related. The study sought to analyze differences in gene expression between periodontitis patients before and after treatment using bioinformatics techniques. METHODS: The GSE6751 data set was screened for differentially expressed genes (DEGs) and immune-related genes using the Gene Expression Omnibus (GEO) database, a gene expression data analysis tool. Enrichment, protein-protein interaction (PPI) network construction, and immune cell correlation analyses were also performed on these genes. RESULTS: A total of 327 DEGs in periodontitis were identified, including 149 upregulated genes, 178 downregulated genes, and 27 immune-related genes. The immune-related DEGs were mainly involved in granulocyte chemotaxis, granulocyte migration, leukocyte chemotaxis, cytokine receptor binding, Toll-like receptor (TLR) binding, the phosphatidylinositol-3-kinase and protein kinase b signaling pathway, viral protein interactions with cytokines and cytokine receptors, the Ras-proximate-1 signaling pathway, the Ras signaling pathway, natural killer cell mediated cytotoxicity, and immune response related pathways. IFNG and TLR2 were the key core genes in the constructed PPI network. CONCLUSIONS: The pathogenesis of periodontitis is closely related to changes in the expression of genes, such as PF4, ANGPT1, TNFRSF1B, IFNG and TLR2, among which IFNG and TLR2 are potential therapeutic targets for periodontitis. AME Publishing Company 2022-05 /pmc/articles/PMC9201185/ /pubmed/35722384 http://dx.doi.org/10.21037/atm-22-1592 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Ban, Qiang
Ling, Xiaofang
Ding, Hui
Meng, Jiansheng
Li, Yuan
Zhang, Juanfei
Zhu, Mingyi
Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
title Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
title_full Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
title_fullStr Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
title_full_unstemmed Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
title_short Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
title_sort screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9201185/
https://www.ncbi.nlm.nih.gov/pubmed/35722384
http://dx.doi.org/10.21037/atm-22-1592
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