Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis

• Published in: Scientific reports Vol. 10; no. 1; p. 16290
• Main Authors: Banaganapalli, Babajan, Mansour, Haifa, Mohammed, Arif, Alharthi, Arwa Mastoor, Aljuaid, Nada Mohammed, Nasser, Khalidah Khalid, Ahmad, Aftab, Saadah, Omar I., Al-Aama, Jumana Yousuf, Elango, Ramu, Shaik, Noor Ahmad
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.10.2020; Nature Publishing Group
• Subjects: 631/114; 631/337; Absorption; Atrophy; Autoimmune diseases; Celiac disease; Celiac Disease - genetics; Celiac Disease - metabolism; Cell cycle; Cell differentiation; Cell division; Cluster analysis; Drug metabolism; Duodenum; Gene expression; Gene Expression Profiling; Gene Expression Regulation - genetics; Gene Regulatory Networks - genetics; Gluten; Helper cells; Humanities and Social Sciences; Humans; Immune system; Interleukin 17; Lymphocytes; Lymphocytes T; Metabolic Networks and Pathways - genetics; Metabolism; Mucosa; multidisciplinary; p53 Protein; Pathogenesis; Pathophysiology; Protein interaction; Protein Interaction Maps - genetics; Science; Science (multidisciplinary); Signal transduction
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-73288-6

Celiac disease (CeD) is a gastrointestinal autoimmune disorder, whose specific molecular basis is not yet fully interpreted. Therefore, in this study, we compared the global gene expression profile of duodenum tissues from CeD patients, both at the time of disease diagnosis and after two years of the gluten-free diet. A series of advanced systems biology approaches like differential gene expression, protein–protein interactions, gene network-cluster analysis were deployed to annotate the candidate pathways relevant to CeD pathogenesis. The duodenum tissues from CeD patients revealed the differential expression of 106 up- and 193 down-regulated genes. The pathway enrichment of differentially expressed genes (DEGs) highlights the involvement of biological pathways related to loss of cell division regulation (cell cycle, p53 signalling pathway), immune system processes (NOD-like receptor signalling pathway, Th1, and Th2 cell differentiation, IL-17 signalling pathway) and impaired metabolism and absorption (mineral and vitamin absorptions and drug metabolism) in celiac disease. The molecular dysfunctions of these 3 biological events tend to increase the number of intraepithelial lymphocytes (IELs) and villous atrophy of the duodenal mucosa promoting the development of CeD. For the first time, this study highlights the involvement of aberrant cell division, immune system, absorption, and metabolism pathways in CeD pathophysiology and presents potential novel therapeutic opportunities.