• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Elevated circulating miR-150 and miR-342-3p in patients with irritable bowel syndrome.肠易激综合征患者循环 miR-150 和 miR-342-3p 水平升高。
Exp Mol Pathol. 2014 Jun;96(3):422-5. doi: 10.1016/j.yexmp.2014.04.009. Epub 2014 Apr 21.
2
The Colonic Mucosal MicroRNAs, MicroRNA-219a-5p, and MicroRNA-338-3p Are Downregulated in Irritable Bowel Syndrome and Are Associated With Barrier Function and MAPK Signaling.肠道黏膜 MicroRNAs,miR-219a-5p 和 miR-338-3p 在肠易激综合征中下调,与屏障功能和 MAPK 信号有关。
Gastroenterology. 2021 Jun;160(7):2409-2422.e19. doi: 10.1053/j.gastro.2021.02.040. Epub 2021 Feb 20.
3
Serum microRNA array analysis identifies miR-140-3p, miR-33b-3p and miR-671-3p as potential osteoarthritis biomarkers involved in metabolic processes.血清 microRNA 芯片分析鉴定出 miR-140-3p、miR-33b-3p 和 miR-671-3p 作为潜在的与代谢过程相关的骨关节炎生物标志物。
Clin Epigenetics. 2017 Dec 12;9:127. doi: 10.1186/s13148-017-0428-1. eCollection 2017.
4
Differential expression of microRNA related to irritable bowel syndrome in a rabbit model.兔肠易激综合征模型中与肠易激综合征相关的微小RNA的差异表达
J Dig Dis. 2017 Jun;18(6):330-342. doi: 10.1111/1751-2980.12485.
5
Identification of plasma miR-4505, miR-4743-5p and miR-4750-3p as novel diagnostic biomarkers for coronary artery disease in patients with type 2 diabetes mellitus: a case-control study.鉴定血浆 miR-4505、miR-4743-5p 和 miR-4750-3p 作为 2 型糖尿病患者冠心病的新型诊断生物标志物:病例对照研究。
Cardiovasc Diabetol. 2024 Jul 29;23(1):278. doi: 10.1186/s12933-024-02374-0.
6
miR-16 and miR-125b are involved in barrier function dysregulation through the modulation of claudin-2 and cingulin expression in the jejunum in IBS with diarrhoea.miR-16和miR-125b通过调节腹泻型肠易激综合征患者空肠中claudin-2和cingulin的表达参与屏障功能失调。
Gut. 2017 Sep;66(9):1537-1538. doi: 10.1136/gutjnl-2016-311477. Epub 2017 Jan 12.
7
Regulation of serum microRNA expression by acupuncture in patients with diarrhea-predominant irritable bowel syndrome.针刺对腹泻型肠易激综合征患者血清微小 RNA 表达的调控。
Acupunct Med. 2022 Feb;40(1):34-42. doi: 10.1177/09645284211027892. Epub 2021 Jul 7.
8
Circulating microRNAs as biomarkers of adult Crohn's disease.循环微RNA作为成人克罗恩病的生物标志物
Eur J Gastroenterol Hepatol. 2015 Sep;27(9):1038-44. doi: 10.1097/MEG.0000000000000430.
9
Identification of Potential MicroRNA-MRNA Regulatory Relationship Pairs in Irritable Bowel Syndrome with Diarrhea.识别腹泻型肠易激综合征中潜在的 miRNA-mRNA 调控关系对。
Comb Chem High Throughput Screen. 2023;26(8):1618-1628. doi: 10.2174/1386207326666230109143325.
10
MicroRNA profiling reveals dysregulated microRNAs and their target gene regulatory networks in cemento-ossifying fibroma.miRNA 谱分析揭示骨化性纤维瘤中失调的 microRNAs 及其靶基因调控网络。
J Oral Pathol Med. 2018 Jan;47(1):78-85. doi: 10.1111/jop.12650. Epub 2017 Nov 1.

引用本文的文献

1
The Interplay Between Immunological Status and Gut Microbial Dysbiosis in the Development of the Symptoms of Irritable Bowel Syndrome: A Systematic Review with Meta-Analysis.免疫状态与肠道微生物群失调在肠易激综合征症状发展中的相互作用:一项系统评价与荟萃分析
Dig Dis Sci. 2025 Sep 3. doi: 10.1007/s10620-025-09360-w.
2
Therapeutic Implication of miRNAs as an Active Regulatory Player in the Management of Pain: A Review.miRNAs 在疼痛管理中的治疗意义:综述。
Genes (Basel). 2024 Jul 31;15(8):1003. doi: 10.3390/genes15081003.
3
Global research states and trends of micro RNA in irritable bowel syndrome: a bibliometric analysis.全球研究表明,肠易激综合征中 micro RNA 的状态和趋势:文献计量分析。
Clin Exp Med. 2024 Jul 5;24(1):149. doi: 10.1007/s10238-024-01396-y.
4
Cytolethal distending toxin B inoculation leads to distinct gut microtypes and IBS-D-like microRNA-mediated gene expression changes in a rodent model.细胞致死扩张毒素 B 接种导致肠道微类型的明显差异和 IBS-D 样 microRNA 介导的基因表达变化在啮齿动物模型中。
Gut Microbes. 2024 Jan-Dec;16(1):2293170. doi: 10.1080/19490976.2023.2293170. Epub 2023 Dec 18.
5
Integrated omics analysis reveals the epigenetic mechanism of visceral hypersensitivity in IBS-D.综合组学分析揭示腹泻型肠易激综合征内脏高敏感性的表观遗传机制。
Front Pharmacol. 2023 Mar 16;14:1062630. doi: 10.3389/fphar.2023.1062630. eCollection 2023.
6
MicroRNAs in Inflammatory Bowel Disease and Its Complications.炎症性肠病及其并发症中的 microRNAs。
Int J Mol Sci. 2022 Aug 6;23(15):8751. doi: 10.3390/ijms23158751.
7
Developmental Alterations of Colonic microRNA Profiles Imply Potential Biological Functions in Kid Goats.结肠微小RNA谱的发育变化暗示了幼山羊的潜在生物学功能。
Animals (Basel). 2022 Jun 14;12(12):1533. doi: 10.3390/ani12121533.
8
Functional Implications and Clinical Potential of MicroRNAs in Irritable Bowel Syndrome: A Concise Review.功能性影响和临床潜力的 microRNAs 在肠易激综合征:一个简洁的回顾。
Dig Dis Sci. 2023 Jan;68(1):38-53. doi: 10.1007/s10620-022-07516-6. Epub 2022 May 4.
9
Profiling Blood Serum Extracellular Vesicles in Plaque Psoriasis and Psoriatic Arthritis Patients Reveals Potential Disease Biomarkers.斑块状银屑病和银屑病关节炎患者血清外泌体分析揭示潜在疾病生物标志物。
Int J Mol Sci. 2022 Apr 4;23(7):4005. doi: 10.3390/ijms23074005.
10
Single-Molecule Sensor for High-Confidence Detection of miRNA.用于高置信度检测 miRNA 的单分子传感器。
ACS Sens. 2022 Apr 22;7(4):1086-1094. doi: 10.1021/acssensors.1c02748. Epub 2022 Mar 21.

本文引用的文献

1
Functional bowel symptoms in quiescent inflammatory bowel diseases: role of epithelial barrier disruption and low-grade inflammation.静止期炎症性肠病中的功能性肠病症状:上皮屏障破坏和低水平炎症的作用。
Gut. 2014 May;63(5):744-52. doi: 10.1136/gutjnl-2012-304066. Epub 2013 Jul 22.
2
Inverse relationship of interleukin-6 and mast cells in children with inflammatory and non-inflammatory abdominal pain phenotypes.炎症性和非炎症性腹痛表型儿童中白细胞介素-6与肥大细胞的负相关关系。
World J Gastrointest Pathophysiol. 2012 Dec 15;3(6):102-8. doi: 10.4291/wjgp.v3.i6.102.
3
Deciphering microRNA code in pain and inflammation: lessons from bladder pain syndrome.解析疼痛和炎症中的 microRNA 密码:从膀胱疼痛综合征中得到的启示。
Cell Mol Life Sci. 2013 Oct;70(20):3773-89. doi: 10.1007/s00018-013-1275-7. Epub 2013 Mar 5.
4
Alternative splicing: functional diversity among voltage-gated calcium channels and behavioral consequences.可变剪接:电压门控钙通道的功能多样性及行为后果
Biochim Biophys Acta. 2013 Jul;1828(7):1522-9. doi: 10.1016/j.bbamem.2012.09.018. Epub 2012 Sep 26.
5
SERT and TPH-1 mRNA expression are reduced in irritable bowel syndrome patients regardless of visceral sensitivity state in large intestine.无论大肠内脏敏感性状态如何,肠易激综合征患者 SERT 和 TPH-1 mRNA 的表达均降低。
Am J Physiol Gastrointest Liver Physiol. 2012 May 1;302(9):G1053-60. doi: 10.1152/ajpgi.00153.2011. Epub 2012 Feb 9.
6
MicroRNA modulation in complex regional pain syndrome.复杂区域性疼痛综合征中的 microRNA 调节。
J Transl Med. 2011 Nov 10;9:195. doi: 10.1186/1479-5876-9-195.
7
miR-150 as a potential biomarker associated with prognosis and therapeutic outcome in colorectal cancer.miR-150 作为一种与结直肠癌预后和治疗结果相关的潜在生物标志物。
Gut. 2012 Oct;61(10):1447-53. doi: 10.1136/gutjnl-2011-301122. Epub 2011 Nov 3.
8
miRNA-based therapies for the irritable bowel syndrome.基于 microRNA 的肠易激综合征治疗方法。
Expert Opin Biol Ther. 2011 Aug;11(8):991-5. doi: 10.1517/14712598.2011.577060. Epub 2011 Apr 11.
9
MicroRNAs in inflammatory bowel disease.炎症性肠病中的 microRNAs。
Inflamm Bowel Dis. 2012 Jan;18(1):187-93. doi: 10.1002/ibd.21691. Epub 2011 Mar 18.
10
Caught in the Akt: regulation of Wnt signaling in the intestine.深陷Akt之中:肠道中Wnt信号通路的调控
Gastroenterology. 2010 Sep;139(3):718-22. doi: 10.1053/j.gastro.2010.07.012. Epub 2010 Jul 24.

肠易激综合征患者循环 miR-150 和 miR-342-3p 水平升高。

Elevated circulating miR-150 and miR-342-3p in patients with irritable bowel syndrome.

机构信息

Digestive Disorders Unit, National Institute of Nursing Research, National Institutes of Health, DHHS, Bethesda, MD 20892, United States.

Digestive Disorders Unit, National Institute of Nursing Research, National Institutes of Health, DHHS, Bethesda, MD 20892, United States; Howard Hughes Medical Institute National Institutes of Health Research Scholar, Chevy Chase, MD 20815, United States.

出版信息

Exp Mol Pathol. 2014 Jun;96(3):422-5. doi: 10.1016/j.yexmp.2014.04.009. Epub 2014 Apr 21.

DOI:10.1016/j.yexmp.2014.04.009
PMID:24768587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4119883/
Abstract

BACKGROUND AND AIMS

MicroRNAs (miRNAs) are small non-coding RNAs, which regulate gene expression and are thus of interest as diagnostic markers, and as clues to etiology and targets of intervention. This pilot study examined whether circulating miRNAs are differentially expressed in patients with IBS.

METHODS

miRNA microarrays (NanoString) were run on the whole blood of 43 participants.

RESULTS

hsa-miR-150 and hsa-miR-342-3p were found to be significantly elevated (FDR adjusted p≤0.05, ≥1.6 fold change) in IBS patients compared to healthy controls. Neither of these miRNAs showed any relationship to race or sex. hsa-miR-150 is associated with inflammatory bowel disorders and pain, and interacts with a protein kinase (AKT2) through which it may affect inflammatory pathways. hsa-miR-342-3p is predicted to interact with mRNAs involved in pain signaling, colonic motility, and smooth muscle function.

CONCLUSIONS

This preliminary study reports the association of two miRNAs, detected in whole blood, with IBS. These miRNAs link to pain and inflammatory pathways both of which are thought to be dysregulated in IBS. Larger sample sizes are needed to confirm their importance and potential as biomarkers.

摘要

背景和目的

微小 RNA(miRNA)是一种小的非编码 RNA,可调节基因表达,因此作为诊断标志物、病因线索和干预靶点而受到关注。本初步研究旨在探讨循环 miRNA 是否在 IBS 患者中存在差异表达。

方法

对 43 名参与者的全血进行 miRNA 微阵列(NanoString)检测。

结果

与健康对照组相比,IBS 患者的 hsa-miR-150 和 hsa-miR-342-3p 显著升高(FDR 调整的 p 值≤0.05,倍数变化≥1.6)。这两种 miRNA 均与种族或性别无关。hsa-miR-150 与炎症性肠病和疼痛有关,并且通过与蛋白激酶(AKT2)相互作用,可能影响炎症途径。hsa-miR-342-3p 被预测与涉及疼痛信号传导、结肠运动和平滑肌功能的 mRNA 相互作用。

结论

本初步研究报告了两种 miRNA 的关联,这些 miRNA 在全血中被检测到,与 IBS 相关。这些 miRNA 与疼痛和炎症途径相关,而这些途径在 IBS 中被认为失调。需要更大的样本量来确认它们作为生物标志物的重要性和潜力。