Differentially Expressed miRNAs in Ulcerative Colitis and Crohn's Disease
- PMID: 35734163
- PMCID: PMC9208551
- DOI: 10.3389/fimmu.2022.865777
Differentially Expressed miRNAs in Ulcerative Colitis and Crohn's Disease
Abstract
Differential microRNA (miRNA or miR) regulation is linked to the development and progress of many diseases, including inflammatory bowel disease (IBD). It is well-established that miRNAs are involved in the differentiation, maturation, and functional control of immune cells. miRNAs modulate inflammatory cascades and affect the extracellular matrix, tight junctions, cellular hemostasis, and microbiota. This review summarizes current knowledge of differentially expressed miRNAs in mucosal tissues and peripheral blood of patients with ulcerative colitis and Crohn's disease. We combined comprehensive literature curation with computational meta-analysis of publicly available high-throughput datasets to obtain a consensus set of miRNAs consistently differentially expressed in mucosal tissues. We further describe the role of the most relevant differentially expressed miRNAs in IBD, extract their potential targets involved in IBD, and highlight their diagnostic and therapeutic potential for future investigations.
Keywords: Crohn’s disease; Transcriptomics; inflammatory bowel disase; miRNA; ulcerative colitis.
Copyright © 2022 Yarani, Shojaeian, Palasca, Doncheva, Jensen, Gorodkin and Pociot.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures


Similar articles
-
MicroRNAs expression influence in ulcerative colitis and Crohn's disease: A pilot study for the identification of diagnostic biomarkers.World J Gastroenterol. 2021 Dec 7;27(45):7801-7812. doi: 10.3748/wjg.v27.i45.7801. World J Gastroenterol. 2021. PMID: 34963743 Free PMC article.
-
Plasma microRNA Profile Differentiates Crohn's Colitis From Ulcerative Colitis.Inflamm Bowel Dis. 2017 Dec 19;24(1):159-165. doi: 10.1093/ibd/izx009. Inflamm Bowel Dis. 2017. PMID: 29272478 Free PMC article.
-
MicroRNA signatures differentiate Crohn's disease from ulcerative colitis.BMC Immunol. 2015 Feb 10;16:5. doi: 10.1186/s12865-015-0069-0. BMC Immunol. 2015. PMID: 25886994 Free PMC article.
-
Deep Dive Into MicroRNAs in Inflammatory Bowel Disease.Inflamm Bowel Dis. 2023 Jun 1;29(6):986-999. doi: 10.1093/ibd/izac250. Inflamm Bowel Dis. 2023. PMID: 36545755 Review.
-
Intestinal Microbiota and miRNA in IBD: A Narrative Review about Discoveries and Perspectives for the Future.Int J Mol Sci. 2023 Apr 13;24(8):7176. doi: 10.3390/ijms24087176. Int J Mol Sci. 2023. PMID: 37108339 Free PMC article. Review.
Cited by
-
Heparin-binding EGF-like growth factor via miR-126 controls tumor formation/growth and the proteolytic niche in murine models of colorectal and colitis-associated cancers.Cell Death Dis. 2024 Oct 17;15(10):753. doi: 10.1038/s41419-024-07126-2. Cell Death Dis. 2024. PMID: 39419989 Free PMC article.
-
Cross-species high-resolution transcriptome profiling suggests biomarkers and therapeutic targets for ulcerative colitis.Front Mol Biosci. 2023 Jan 5;9:1081176. doi: 10.3389/fmolb.2022.1081176. eCollection 2022. Front Mol Biosci. 2023. PMID: 36685283 Free PMC article.
-
Multi-omics in Crohn's disease: New insights from inside.Comput Struct Biotechnol J. 2023 May 13;21:3054-3072. doi: 10.1016/j.csbj.2023.05.010. eCollection 2023. Comput Struct Biotechnol J. 2023. PMID: 37273853 Free PMC article. Review.
-
A prediction of the CRNDE role by modulating NF-κB pathway in inflammatory bowel disease (IBD).Biochem Biophys Rep. 2024 May 11;38:101731. doi: 10.1016/j.bbrep.2024.101731. eCollection 2024 Jul. Biochem Biophys Rep. 2024. PMID: 38766384 Free PMC article.
-
Gut Microbiome and Small RNA Integrative-Omic Perspective of Meconium and Milk-FED Infant Stool Samples.Int J Mol Sci. 2023 Apr 29;24(9):8069. doi: 10.3390/ijms24098069. Int J Mol Sci. 2023. PMID: 37175775 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical