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Perturbations of Circulating miRNAs in Irritable Bowel Syndrome Detected Using a Multiplexed High-throughput Gene Expression Platform
Published on: November 30, 2016
Identification of potential molecular pathogenesis mechanisms modulated by microRNAs in patients with Intestinal
Marcos C Angelini1, Alana Maia E Silva1, Tainara F Felix1,2
1UNESP - São Paulo State University, Faculty of Medicine, Department of Surgery and Orthopedics, Botucatu, SP, Brazil.
Abstract:
This study proposed to determine global microRNA (miRNA) expression and miRNA-regulated pathways in Intestinal Neuronal Dysplasia type B (IND-B). Fifty patients (0-15 years old) with IND-B were included in the study. Peripheral blood samples were collected from all 50 patients and from 10 healthy asymptomatic children (controls). Rectal biopsies were collected from 29/50 patients; biopsy tissues were needle microdissected to isolate the different intestinal layers, for molecular analysis. Global miRNA expression was determined using TaqMan arrays. Correlation analysis between miRNA expression in plasma and biopsy samples as well as among tissues derived from the distinct intestinal layers was performed. Computational approaches were used for miRNA target prediction/identification of miRNA-regulated genes and enriched pathways biologically relevant to IND-B pathogenesis. miRNAs were statistically significantly deregulated (FC ≥ 2 and p ≤ 0.05) in submucosal and muscular layers: over-expressed (miR-146a and miR-146b) and under-expressed (miR-99a, miR-100, miR-130a, miR-133b, miR-145, miR-365, miR-374-5p, miR-451). Notably, let-7a-5p was highly over-expressed in patient plasma compared to healthy controls (FC = 17.4). In addition, miR-451 was significantly under-expressed in both plasma and all biopsy tissues from the same patients. Enriched pathways (p < 0.01) were axon guidance, nerve growth factor signalling, NCAM signalling for neurite out-growth, neuronal system and apoptosis. miRNA expression is deregulated in the submucosa and muscular layers of the rectum and detected in plasma from patients with IND-B. Biologically enriched pathways regulated by the identified miRNAs may play a role in IND-B disease pathogenesis, due to the activity related to the neurons of the enteric nervous system.
Insights
MicroRNA (miRNA) expression is altered in Intestinal Neuronal Dysplasia type B (IND-B) patients. Deregulated miRNAs in rectal tissues and plasma may indicate pathways involved in enteric nervous system development and IND-B pathogenesis.
Area of Science:
- Gastroenterology and Molecular Biology
- Pediatric Disease Research
- Neuroscience and Genetics
Background:
- Intestinal Neuronal Dysplasia type B (IND-B) is a congenital disorder affecting the enteric nervous system.
- Understanding the molecular mechanisms underlying IND-B is crucial for diagnosis and treatment.
- MicroRNAs (miRNAs) are key regulators of gene expression implicated in various diseases.
Purpose of the Study:
- To determine global miRNA expression profiles in patients with IND-B.
- To identify miRNA-regulated pathways involved in IND-B pathogenesis.
- To correlate miRNA expression in plasma and rectal tissues.
Main Methods:
- Analysis of miRNA expression in plasma and rectal biopsy samples from 50 IND-B patients and 10 controls.
- Microdissection of rectal tissues to isolate intestinal layers for molecular analysis.
- TaqMan arrays for global miRNA expression, computational analysis for target prediction and pathway enrichment.
Main Results:
- Statistically significant deregulation of specific miRNAs (e.g., miR-146a/b, miR-99a, miR-451) in submucosal and muscular rectal layers.
- Over-expression of let-7a-5p in patient plasma and under-expression of miR-451 in both plasma and tissues.
- Enrichment of pathways related to axon guidance, neurotrophic signaling, and neuronal development.
Conclusions:
- miRNA expression is significantly altered in the rectal submucosa and muscularis of IND-B patients.
- Plasma and tissue miRNA profiles offer potential biomarkers for IND-B.
- Identified miRNA-regulated pathways are biologically relevant to enteric nervous system function and IND-B pathogenesis.
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