Résumé
Aim: Aim of this study is screen of the large numbers of related genes of CD to find the key ones
Background: Celiac disease [CD] is known as a gluten sensitive and immune system dependent disease. There are several high throughput investigations about CD but it is necessary to clarify new molecular aspects mechanism of celiac
Methods: Whole-genome profile [RNA] of the human peripheral blood mononuclear cells [PBMCs] as Gene expression profile GSE113469 was retrieved Gene Expression Omnibus [GEO] database. The significant genes were selected and analyzed via proteinprotein interaction [PPI] network by Cytoscape software. The key genes were introduced and enriched via ClueGO to find the related biochemical pathways
Results: Among 250 significant genes 47 genes with expressed change above 2 fold change [FC] were interacted and the constructed network were analyzed. The network characterized by poor connections so it was promoted by addition 50 related nodes and 18 crucial nodes were introduced. Two clusters of biochemical pathways were identified and discussed
Conclusion: There is an obvious conflict between microarray finding and the well-known related genes of CD. This problem can be solve by more attention to the interpretation of PPI ntwork analysis results