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Updated: Mar 20, 2026

Perturbations of Circulating miRNAs in Irritable Bowel Syndrome Detected Using a Multiplexed High-throughput Gene Expression Platform
Published on: November 30, 2016
Small Interfering Ribonucleic Acid (siRNA)-Based Therapeutics in Inflammatory Bowel Disease: Crosstalk between Immune
Mansi Patel1, Bhagyabhumi Shah1
1Department of Pharmacology, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, CHARUSAT Campus, Changa, Gujarat 388 421, India.
Small interfering RNA (siRNA) therapies offer a precise approach to treating inflammatory bowel disease (IBD) by targeting specific genes. This review highlights siRNA
Area of Science:
- Gastroenterology
- Immunology
- RNA Therapeutics
Background:
- Inflammatory bowel disease (IBD), including ulcerative colitis and Crohn's disease, involves immune dysregulation, barrier dysfunction, and microbial imbalance.
- Current IBD treatments like corticosteroids, immunomodulators, and biologics have limitations including nonspecific action, side effects, and suboptimal remission rates.
Purpose of the Study:
- To review recent advancements in small interfering RNA (siRNA) therapies for IBD.
- To explore siRNA's potential in immune modulation and epithelial barrier restoration for IBD treatment.
Main Methods:
- Review of current literature on siRNA applications in IBD.
- Analysis of siRNA's mechanisms targeting inflammatory pathways and mucosal barrier integrity.
Main Results:
- siRNA effectively silences genes encoding proinflammatory cytokines (e.g., TNF-α, IL-6) and signaling pathways (e.g., NF-κB, JAK/STAT).
- siRNA enhances mucosal barrier function by targeting tight junction proteins (e.g., ZO-1, occludin).
- Combination siRNA therapies show promise for IBD management.
Conclusions:
- siRNA represents a precision-driven therapeutic strategy for IBD with potential for immune modulation and barrier repair.
- Further clinical translation is necessary to establish the safety and efficacy of siRNA therapies for IBD.
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