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炎症性肠病中的 microRNAs:我们知道什么,我们可以期待什么?

MicroRNAs in inflammatory bowel disease: What do we know and what can we expect?

机构信息

Department of Internal Medicine, Medical School, São Paulo State University (Unesp), Botucatu 18618-686, São Paulo, Brazil.

Verum Ingredients, Botucatu Technology Park, Botucatu 18605-525, São Paulo, Brazil.

出版信息

World J Gastroenterol. 2024 Apr 28;30(16):2184-2190. doi: 10.3748/wjg.v30.i16.2184.


DOI:10.3748/wjg.v30.i16.2184
PMID:38690020
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11056918/
Abstract

MicroRNAs (miRNAs), small non-coding RNAs composed of 18-24 nucleotides, are potent regulators of gene expression, contributing to the regulation of more than 30% of protein-coding genes. Considering that miRNAs are regulators of inflammatory pathways and the differentiation of intestinal epithelial cells, there is an interest in exploring their importance in inflammatory bowel disease (IBD). IBD is a chronic and multifactorial disease of the gastrointestinal tract; the main forms are Crohn's disease and ulcerative colitis. Several studies have investigated the dysregulated expression of miRNAs in IBD, demonstrating their important roles as regulators and potential biomarkers of this disease. This editorial presents what is known and what is expected regarding miRNAs in IBD. Although the important regulatory roles of miRNAs in IBD are clearly established, biomarkers for IBD that can be applied in clinical practice are lacking, emphasizing the importance of further studies. Discoveries regarding the influence of miRNAs on the inflammatory process and the exploration of their role in gene regulation are expected to provide a basis for the use of miRNAs not only as potent biomarkers in IBD but also as therapeutic targets for the control of inflammatory processes in personalized medicine.

摘要

微小 RNA(miRNAs)是由 18-24 个核苷酸组成的小非编码 RNA,是基因表达的有效调节剂,参与调节超过 30%的蛋白质编码基因。鉴于 miRNAs 是炎症途径和肠道上皮细胞分化的调节剂,人们对其在炎症性肠病(IBD)中的重要性产生了兴趣。IBD 是一种慢性和多因素的胃肠道疾病;主要形式是克罗恩病和溃疡性结肠炎。有几项研究调查了 miRNA 在 IBD 中的失调表达,证明了它们作为该疾病调节剂和潜在生物标志物的重要作用。本社论介绍了关于 IBD 中 miRNA 的已知和预期内容。尽管 miRNA 在 IBD 中的重要调节作用已得到明确确立,但缺乏可应用于临床实践的 IBD 生物标志物,这强调了进一步研究的重要性。关于 miRNA 对炎症过程的影响的发现以及对其在基因调控中的作用的探索有望为 miRNA 的应用提供基础,不仅将其作为 IBD 的有效生物标志物,而且还作为个性化医学中控制炎症过程的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f9/11056918/07772eb4f42f/WJG-30-2184-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f9/11056918/07772eb4f42f/WJG-30-2184-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f9/11056918/07772eb4f42f/WJG-30-2184-g001.jpg

相似文献

[1]
MicroRNAs in inflammatory bowel disease: What do we know and what can we expect?

World J Gastroenterol. 2024-4-28

[2]
The crucial role of non-coding RNAs in the pathophysiology of inflammatory bowel disease.

Biomed Pharmacother. 2020-9

[3]
MicroRNAs as Innovative Biomarkers for Inflammatory Bowel Disease and Prediction of Colorectal Cancer.

Int J Mol Sci. 2022-7-20

[4]
Role of MiRNAs in Inflammatory Bowel Disease.

Dig Dis Sci. 2017-6

[5]
Trefoil factors in inflammatory bowel disease.

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[6]
Interplay between Cytokine Circuitry and Transcriptional Regulation Shaping Helper T Cell Pathogenicity and Plasticity in Inflammatory Bowel Disease.

Int J Mol Sci. 2020-5-11

[7]
miRNA Molecules-Late Breaking Treatment for Inflammatory Bowel Diseases?

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[8]
Whole genome gene expression meta-analysis of inflammatory bowel disease colon mucosa demonstrates lack of major differences between Crohn's disease and ulcerative colitis.

PLoS One. 2013-2-13

[9]
Epithelial expression of interleukin-37b in inflammatory bowel disease.

Clin Exp Immunol. 2013-6

[10]
Differential expression of key regulators of Toll-like receptors in ulcerative colitis and Crohn's disease: a role for Tollip and peroxisome proliferator-activated receptor gamma?

Clin Exp Immunol. 2016-3

引用本文的文献

[1]
Ferroptosis in immune chaos: Unraveling its impact on disease and therapeutic potential.

J Physiol Biochem. 2025-4-16

[2]
Chronic Gastrointestinal Disorders and miRNA-Associated Disease: An Up-to-Date.

Int J Mol Sci. 2025-1-6

[3]
Fibrosis-Related microRNAs in Crohn's Disease with Fibrostenosis and Inflammatory Stenosis.

Int J Mol Sci. 2024-8-13

[4]
Interaction between microRNA-195 and HuR regulates Paneth cell function in the intestinal epithelium by altering SOX9 translation.

Am J Physiol Cell Physiol. 2024-9-1

本文引用的文献

[1]
Fecal miR-223 is a noninvasive biomarker for estimating Crohn's disease activity.

Immun Inflamm Dis. 2023-12

[2]
Expression of Circulating let-7e and miR-126 May Predict Clinical Remission in Patients With Crohn's Disease Treated With Anti-TNF-α Biologics.

Inflamm Bowel Dis. 2024-3-1

[3]
MiR-126-Loaded Immunoliposomes against Vascular Endothelial Inflammation In Vitro and Vivo Evaluation.

Pharmaceutics. 2023-4-30

[4]
Intestinal Microbiota and miRNA in IBD: A Narrative Review about Discoveries and Perspectives for the Future.

Int J Mol Sci. 2023-4-13

[5]
Positioning and Usefulness of Biomarkers in Inflammatory Bowel Disease.

Digestion. 2023

[6]
Deficiency of miRNA-149-3p shaped gut microbiota and enhanced dextran sulfate sodium-induced colitis.

Mol Ther Nucleic Acids. 2022-9-24

[7]
ABX464 (obefazimod) for moderate-to-severe, active ulcerative colitis: a phase 2b, double-blind, randomised, placebo-controlled induction trial and 48 week, open-label extension.

Lancet Gastroenterol Hepatol. 2022-11

[8]
Activating IL-6/STAT3 Enhances Protein Stability of Proteasome 20S + in Colorectal Cancer by miR-1254.

Biomed Res Int. 2022

[9]
Inflammatory bowel disease biomarkers.

Med Res Rev. 2022-9

[10]
ECCO Guidelines on Therapeutics in Ulcerative Colitis: Medical Treatment.

J Crohns Colitis. 2022-1-28

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