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基于 microRNA 的肠易激综合征治疗方法。

miRNA-based therapies for the irritable bowel syndrome.

出版信息

Expert Opin Biol Ther. 2011 Aug;11(8):991-5. doi: 10.1517/14712598.2011.577060. Epub 2011 Apr 11.

DOI:10.1517/14712598.2011.577060
PMID:21476882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3126904/
Abstract

The irritable bowel syndrome (IBS) is a common disorder of unknown etiology. Recently, a group of dysregulated microRNAs (miRNAs) in blood microvesicles and in colon tissue have been identified in IBS patients. miRNAs have been shown to modulate specific biological processes such as differentiation, proliferation, apoptosis and metabolism. The ideal strategy would be to use specific miRNAs as both diagnostic and therapeutic tools to recover intestinal function and treat intractable gastrointestinal symptoms. In conclusion, further study of the functional role of miRNAs will lead to a better understanding of the dysregulation of intestinal pathways in IBS patients. The results may lead to preventive and/or therapeutic strategies that use small molecules (such as mimics or inhibitors of specific miRNAs) to affect genetic and epigenetic control. Future clinical trials may use microvesicle-associated miRNA-based therapies by using specific inhibitors/mimics of miRNA to target gene expression and treat IBS.

摘要

肠易激综合征(IBS)是一种病因不明的常见疾病。最近,在 IBS 患者的血液微泡和结肠组织中发现了一组失调的 microRNAs(miRNAs)。miRNAs 已被证明可以调节特定的生物学过程,如分化、增殖、凋亡和代谢。理想的策略是将特定的 miRNAs 用作诊断和治疗工具,以恢复肠道功能并治疗难治性胃肠道症状。总之,对 miRNAs 功能作用的进一步研究将导致对 IBS 患者肠道途径失调的更好理解。研究结果可能会导致使用小分子(如特定 miRNAs 的模拟物或抑制剂)来影响遗传和表观遗传控制的预防和/或治疗策略。未来的临床试验可能会使用基于微泡相关 miRNA 的治疗方法,通过使用特定的 miRNA 抑制剂/模拟物来靶向基因表达并治疗 IBS。

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Nat Immunol. 2011 Mar;12(3):239-46. doi: 10.1038/ni.1994. Epub 2011 Jan 30.
2
Targeting microRNAs in cancer: rationale, strategies and challenges.靶向癌症中的 microRNAs:原理、策略和挑战。
Nat Rev Drug Discov. 2010 Oct;9(10):775-89. doi: 10.1038/nrd3179.
3
Role of microRNA in IBS with increased gut permeability.微小RNA在肠道通透性增加的肠易激综合征中的作用。
Gut. 2010 Jun;59(6):710-2. doi: 10.1136/gut.2009.203695.
4
MicroRNA-29a regulates intestinal membrane permeability in patients with irritable bowel syndrome.MicroRNA-29a 调节肠易激综合征患者的肠道黏膜通透性。
Gut. 2010 Jun;59(6):775-84. doi: 10.1136/gut.2009.181834. Epub 2009 Dec 1.
5
Understanding measurements of intestinal permeability in healthy humans with urine lactulose and mannitol excretion.了解健康人体中通过尿液乳果糖和甘露醇排泄来测量肠道通透性。
Neurogastroenterol Motil. 2010 Jan;22(1):e15-26. doi: 10.1111/j.1365-2982.2009.01361.x. Epub 2009 Jul 13.
6
Intestinal membrane permeability and hypersensitivity in the irritable bowel syndrome.肠易激综合征中的肠黏膜通透性与超敏反应
Pain. 2009 Nov;146(1-2):41-6. doi: 10.1016/j.pain.2009.06.017.
7
MicroRNAs are differentially expressed in ulcerative colitis and alter expression of macrophage inflammatory peptide-2 alpha.微小RNA在溃疡性结肠炎中差异表达,并改变巨噬细胞炎性肽-2α的表达。
Gastroenterology. 2008 Nov;135(5):1624-1635.e24. doi: 10.1053/j.gastro.2008.07.068. Epub 2008 Aug 3.
8
First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome.首次发现血清素受体3E型基因的微小RNA - 510靶位点功能性变异与腹泻型肠易激综合征之间存在关联的证据。
Hum Mol Genet. 2008 Oct 1;17(19):2967-77. doi: 10.1093/hmg/ddn195. Epub 2008 Jul 9.
9
Effect of alcohol on miR-212 expression in intestinal epithelial cells and its potential role in alcoholic liver disease.酒精对肠上皮细胞中miR-212表达的影响及其在酒精性肝病中的潜在作用。
Alcohol Clin Exp Res. 2008 Feb;32(2):355-64. doi: 10.1111/j.1530-0277.2007.00584.x. Epub 2007 Dec 21.
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Proc Natl Acad Sci U S A. 2007 Oct 2;104(40):15805-10. doi: 10.1073/pnas.0707628104. Epub 2007 Sep 21.