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克罗恩病纤维化相关 microRNAs 与纤维狭窄和炎症性狭窄。

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

机构信息

Institute of Pathology, Faculty of Medicine, University of Ljubljana, Korytkova 2, 1000 Ljubljana, Slovenia.

出版信息

Int J Mol Sci. 2024 Aug 13;25(16):8826. doi: 10.3390/ijms25168826.


DOI:10.3390/ijms25168826
PMID:39201512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11354456/
Abstract

Crohn's disease (CD) is frequently complicated by strictures that can be either inflammatory or fibrostenotic. This distinction is important for deciding the best treatment course, but it can be difficult to determine clinically, sometimes even by advanced imaging techniques. We performed miRNA PCR panel screening on pooled samples of ileum with CD fibrostenosis or inflammatory stenosis. Eight miRNAs with profibrotic (, and ), or fibroprotective (, , , and ) functions described in the literature were selected for validation on 20 samples each of CD with fibrostenosis or inflammatory stenosis, with a separate sampling of the submucosa and subserosa. The results showed significant differences between the groups in subserosal samples, with upregulation of profibrotic miRNAs and downregulation of fibroprotective miRNAs in fibrostenosis compared to inflammatory stenosis. Only showed a significant difference in the submucosa. There were significant differences in miRNA expression between subserosa and submucosa. Our results provide further evidence that the major differences between fibrostenosis and inflammatory stenosis are located in the subserosa, which is inaccessible to endoscopic sampling, highlighting the need for cross-sectional imaging or serological markers. We identify several miRNAs previously not connected to fibrosis in CD, which could potentially serve as biomarkers of fibrostenosis.

摘要

克罗恩病(CD)常伴有狭窄,可分为炎症性或纤维性狭窄。这种区别对于决定最佳治疗方案很重要,但临床上有时甚至通过先进的成像技术也难以确定,我们对患有 CD 纤维性狭窄或炎症性狭窄的回肠进行了 miRNA PCR 小组筛选。选择了具有文献中描述的致纤维增生(、和)或纤维保护(、、、和)功能的 8 种 miRNA 进行验证,对 20 例纤维性狭窄或炎症性狭窄的 CD 样本进行了验证,对黏膜下层和浆膜层进行了单独取样。结果显示,在浆膜层样本中,纤维化组的致纤维增生 miRNA 上调,纤维保护 miRNA 下调,与炎症性狭窄相比差异显著。仅在黏膜下层中显示出显著差异。黏膜下层和浆膜层之间的 miRNA 表达存在显著差异。我们的研究结果进一步证明,纤维化与炎症性狭窄之间的主要区别位于浆膜层,浆膜层无法进行内镜取样,这突出了需要进行横断面成像或血清标志物检测。我们鉴定了一些以前与 CD 纤维化无关的 miRNA,它们可能作为纤维化狭窄的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ca/11354456/0d227ec22412/ijms-25-08826-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ca/11354456/27e045374269/ijms-25-08826-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ca/11354456/3e90c41d57b7/ijms-25-08826-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ca/11354456/0d227ec22412/ijms-25-08826-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ca/11354456/27e045374269/ijms-25-08826-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ca/11354456/3e90c41d57b7/ijms-25-08826-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ca/11354456/0d227ec22412/ijms-25-08826-g003.jpg

相似文献

[1]
Fibrosis-Related microRNAs in Crohn's Disease with Fibrostenosis and Inflammatory Stenosis.

Int J Mol Sci. 2024-8-13

[2]
Circulating microRNAs as biomarkers of adult Crohn's disease.

Eur J Gastroenterol Hepatol. 2015-9

[3]
Thrombospondin 2, matrix Gla protein and digital analysis identified distinct fibroblast populations in fibrostenosing Crohn's disease.

Sci Rep. 2024-6-14

[4]
Smooth Muscle Hyperplasia/Hypertrophy is the Most Prominent Histological Change in Crohn's Fibrostenosing Bowel Strictures: A Semiquantitative Analysis by Using a Novel Histological Grading Scheme.

J Crohns Colitis. 2016-6-30

[5]
Low Serum Levels of MicroRNA-19 Are Associated with a Stricturing Crohn's Disease Phenotype.

Inflamm Bowel Dis. 2015-8

[6]
MicroRNA signatures differentiate Crohn's disease from ulcerative colitis.

BMC Immunol. 2015-2-10

[7]
Altered microRNA expression in inflamed and non-inflamed terminal ileal mucosa of adult patients with active Crohn's disease.

J Gastroenterol Hepatol. 2015-1

[8]
Identification of microRNAs associated with ileal and colonic Crohn's disease.

Inflamm Bowel Dis. 2010-10

[9]
MicroRNAs Classify Different Disease Behavior Phenotypes of Crohn's Disease and May Have Prognostic Utility.

Inflamm Bowel Dis. 2015-9

[10]
Eosinophils and IL-33 Perpetuate Chronic Inflammation and Fibrosis in a Pediatric Population with Stricturing Crohn's Ileitis.

Inflamm Bowel Dis. 2015-10

引用本文的文献

[1]
Insights into the Molecular Mechanisms and Novel Therapeutic Strategies of Stenosis Fibrosis in Crohn's Disease.

Biomedicines. 2025-7-21

本文引用的文献

[1]
A Combination of Microarray-Based Profiling and Biocomputational Analysis Identified miR331-3p and hsa-let-7d-5p as Potential Biomarkers of Ulcerative Colitis Progression to Colorectal Cancer.

Int J Mol Sci. 2024-5-23

[2]
Thrombospondin 2, matrix Gla protein and digital analysis identified distinct fibroblast populations in fibrostenosing Crohn's disease.

Sci Rep. 2024-6-14

[3]
MicroRNAs in inflammatory bowel disease: What do we know and what can we expect?

World J Gastroenterol. 2024-4-28

[4]
Fibrosis in IBD: from pathogenesis to therapeutic targets.

Gut. 2024-4-5

[5]
How to Evaluate Fibrosis in IBD?

Diagnostics (Basel). 2023-6-27

[6]
Fibro-Stenosing Crohn's Disease: What Is New and What Is Next?

J Clin Med. 2023-4-22

[7]
Gypenosides suppress fibrosis of the renal NRK-49F cells by targeting miR-378a-5p through the PI3K/AKT signaling pathway.

J Ethnopharmacol. 2023-7-15

[8]
MiR-424/TGIF2-Mediated Pro-Fibrogenic Responses in Oral Submucous Fibrosis.

Int J Mol Sci. 2023-3-18

[9]
miRNA Molecules-Late Breaking Treatment for Inflammatory Bowel Diseases?

Int J Mol Sci. 2023-1-23

[10]
Human umbilical cord mesenchymal stem cell-derived exosomal miR-335-5p attenuates the inflammation and tubular epithelial-myofibroblast transdifferentiation of renal tubular epithelial cells by reducing ADAM19 protein levels.

Stem Cell Res Ther. 2022-7-28

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