A Current State of Proteomics in Adult and Pediatric Inflammatory Bowel Diseases: A Systematic Search and Review.
Ondrej FabianLukas BajerPavel DrastichKarel HarantEva SticovaNikola DaskovaIstvan ModosFilip TichanekMonika CahovaPublished in: International journal of molecular sciences (2023)
Inflammatory bowel diseases (IBD) are systemic immune-mediated conditions with predilection for the gastrointestinal tract and include Crohn's disease and ulcerative colitis. Despite the advances in the fields of basic and applied research, the etiopathogenesis remains largely unknown. As a result, only one third of the patients achieve endoscopic remission. A substantial portion of the patients also develop severe clinical complications or neoplasia. The need for novel biomarkers that can enhance diagnostic accuracy, more precisely reflect disease activity, and predict a complicated disease course, thus, remains high. Genomic and transcriptomic studies contributed substantially to our understanding of the immunopathological pathways involved in disease initiation and progression. However, eventual genomic alterations do not necessarily translate into the final clinical picture. Proteomics may represent a missing link between the genome, transcriptome, and phenotypical presentation of the disease. Based on the analysis of a large spectrum of proteins in tissues, it seems to be a promising method for the identification of new biomarkers. This systematic search and review summarize the current state of proteomics in human IBD. It comments on the utility of proteomics in research, describes the basic proteomic techniques, and provides an up-to-date overview of available studies in both adult and pediatric IBD.
Keyphrases
- ulcerative colitis
- disease activity
- end stage renal disease
- mass spectrometry
- newly diagnosed
- systemic lupus erythematosus
- chronic kidney disease
- rheumatoid arthritis
- ejection fraction
- endothelial cells
- genome wide
- single cell
- peritoneal dialysis
- rna seq
- rheumatoid arthritis patients
- high grade
- ultrasound guided
- early onset
- patient reported outcomes
- risk factors
- childhood cancer
- dna methylation