Evaluation of expression of common genes in the intestine and peripheral blood mononuclear cells (PBMC) associated with celiac disease
- PMID: 33585005
- PMCID: PMC7881404
Evaluation of expression of common genes in the intestine and peripheral blood mononuclear cells (PBMC) associated with celiac disease
Abstract
Aim: this study was conducted to investigate expression of the genes associated with CD in the target tissue in order to estimate contribution of each single gene to development of immune response. Then, the same set of genes was evaluated in peripheral blood mononuclear cells (PBMCs).
Background: Celiac disease (CD) is a chronic systemic autoimmune disease of the small intestine occurring in genetically-susceptible individuals. There are several genes related to immune response.
Methods: For this purpose, the genes related to CD were extracted from public databases (documents of proteomics and microarray-based techniques) and were organized in a protein-protein interaction network using the search tool for retrieval of interacting genes/proteins (STRING) database as a plugin of Cytoscape software version 3.6.0. The main genes were introduced and enriched via ClueGO to find the related biochemical pathways. The network was analyzed, and the most important genes were introduced based on central indices.
Results: Among 20 CD genes as hub and bottleneck nodes, there were 7 genes with common expression in blood and intestinal tissue (C-X-C motif chemokine 11(CXCL11), granzyme B (GZMB), interleukin 15(IL-15), interleukin 17(IL-17A), interleukin 23(IL-23A), t-box transcription factor 21(TBX21), and tumor necrosis factor alpha-induced protein 3(TNFAIP3)).
Conclusion: The enriched biological process related to the central nodes of celiac network indicated that most of hub-bottleneck genes are the well-known ones involved in different types of autoimmune and inflammatory diseases.
Keywords: Autoimmune; Celiac Disease; Inflammatory; Intestinal Tissue; PBMC.
©2020 RIGLD, Research Institute for Gastroenterology and Liver Diseases.
Figures
Similar articles
-
Introducing New Potential Biomarkers for Celiac Disease among the Genes Extracted from General Databases.Middle East J Dig Dis. 2022 Apr;14(2):192-199. doi: 10.34172/mejdd.2022.272. Epub 2022 Apr 30. Middle East J Dig Dis. 2022. PMID: 36619141 Free PMC article.
-
Celiac disease microarray analysis based on System Biology Approach.Gastroenterol Hepatol Bed Bench. 2018 Summer;11(3):216-224. Gastroenterol Hepatol Bed Bench. 2018. PMID: 30013745 Free PMC article.
-
Introducing tumor necrosis factor as a prominent player in celiac disease and type 1 diabetes mellitus.Gastroenterol Hepatol Bed Bench. 2019;12(Suppl1):S123-S129. Gastroenterol Hepatol Bed Bench. 2019. PMID: 32099612 Free PMC article.
-
Chemokine (C-X-C motif) ligand (CXCL)10 in autoimmune diseases.Autoimmun Rev. 2014 Mar;13(3):272-80. doi: 10.1016/j.autrev.2013.10.010. Epub 2013 Nov 2. Autoimmun Rev. 2014. PMID: 24189283 Review.
-
Interleukin-15, a master piece in the immunological jigsaw of celiac disease.Dig Dis. 2015;33(2):122-130. doi: 10.1159/000369521. Epub 2015 Apr 22. Dig Dis. 2015. PMID: 25925912 Review.
Cited by
-
Introducing New Potential Biomarkers for Celiac Disease among the Genes Extracted from General Databases.Middle East J Dig Dis. 2022 Apr;14(2):192-199. doi: 10.34172/mejdd.2022.272. Epub 2022 Apr 30. Middle East J Dig Dis. 2022. PMID: 36619141 Free PMC article.
-
Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease.Front Pediatr. 2022 Feb 14;10:837957. doi: 10.3389/fped.2022.837957. eCollection 2022. Front Pediatr. 2022. PMID: 35237542 Free PMC article.
References
LinkOut - more resources
Full Text Sources