• 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

慢性偏头痛中 miRNA 的描述性特征的生物信息学分析。

Bioinformatic Analysis from a Descriptive Profile of miRNAs in Chronic Migraine.

机构信息

Centro de Investigación Multidisciplinario en Salud, Departamento de Ciencias Biomédicas, Centro Universitario de Tonalá, Universidad de Guadalajara, Tonalá 45425, Mexico.

Instituto de Investigación en Reumatología y del Sistema Músculo Esquelético (IIRSME), Departamento de Biología Molecular y Genómica, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara 44340, Mexico.

出版信息

Int J Mol Sci. 2024 Sep 29;25(19):10491. doi: 10.3390/ijms251910491.

DOI:10.3390/ijms251910491
PMID:39408819
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11477213/
Abstract

Chronic migraines have been described chiefly only from a clinical perspective. However, searching for reliable molecular markers has allowed for the discovery of the expression of different genes mainly associated with inflammation, neuro-vascularization, and pain-related pathways. The interest in microRNAs (miRs) that can regulate the expression of these genes has gained significant relevance since multiple miRs could play a key role in regulating these events. In this study, miRs were searched in samples from patients with chronic migraine, and the inclusion criteria were carefully reviewed. Different bioinformatic tools, such as miRbase, targetscan, miRPath, tissue atlas, and miR2Disease, were used to analyze the samples. Our findings revealed that some of the miRs were expressed more (miR-197, miR-101, miR-92a, miR-375, and miR-146b) and less (miR-133a/b, miR-134, miR-195, and miR-340) than others. We concluded that, during chronic migraine, common pathways, such as inflammation, vascularization, neurodevelopment, nociceptive pain, and pharmacological resistance, were associated with this disease.

摘要

慢性偏头痛主要仅从临床角度进行描述。然而,寻找可靠的分子标志物使得能够发现主要与炎症、神经血管生成和与疼痛相关的途径相关的不同基因的表达。由于多个 microRNAs (miRs) 可以调节这些基因的表达,因此对 microRNAs 的研究具有重要意义,因为这些 microRNAs 可能在调节这些事件中发挥关键作用。在这项研究中,从慢性偏头痛患者的样本中搜索了 miRs,并仔细审查了纳入标准。使用了不同的生物信息学工具,如 miRbase、targetscan、miRPath、组织图谱和 miR2Disease,来分析样本。我们的研究结果表明,一些 miRs 的表达量更高(miR-197、miR-101、miR-92a、miR-375 和 miR-146b)或更低(miR-133a/b、miR-134、miR-195 和 miR-340)。我们得出结论,在慢性偏头痛期间,炎症、血管生成、神经发育、伤害性疼痛和药物耐药性等常见途径与该疾病相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d309/11477213/3f7405d28e3a/ijms-25-10491-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d309/11477213/dd4e04906a61/ijms-25-10491-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d309/11477213/3f7405d28e3a/ijms-25-10491-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d309/11477213/dd4e04906a61/ijms-25-10491-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d309/11477213/3f7405d28e3a/ijms-25-10491-g002.jpg

相似文献

1
Bioinformatic Analysis from a Descriptive Profile of miRNAs in Chronic Migraine.慢性偏头痛中 miRNA 的描述性特征的生物信息学分析。
Int J Mol Sci. 2024 Sep 29;25(19):10491. doi: 10.3390/ijms251910491.
2
microRNAs to Monitor Pain-migraine and Drug Treatment.用于监测疼痛性偏头痛及药物治疗的微小RNA
Microrna. 2017 Dec 6;6(3):152-156. doi: 10.2174/2211536606666170913152821.
3
MicroRNA profiling in women with migraine: effects of CGRP-targeting treatment.偏头痛女性的 microRNA 谱分析:CGRP 靶向治疗的影响。
J Headache Pain. 2024 May 16;25(1):80. doi: 10.1186/s10194-024-01787-2.
4
Unbiased Profile of MicroRNA Expression in Ascending Aortic Aneurysm Tissue Appoints Molecular Pathways Contributing to the Pathology.升主动脉瘤组织中微小RNA表达的无偏倚概况确定了导致该病理过程的分子途径。
Ann Thorac Surg. 2016 Oct;102(4):1245-52. doi: 10.1016/j.athoracsur.2016.03.061. Epub 2016 May 25.
5
Integrative molecular bioinformatics study of human adrenocortical tumors: microRNA, tissue-specific target prediction, and pathway analysis.人类肾上腺皮质肿瘤的整合分子生物信息学研究:微小RNA、组织特异性靶标预测及通路分析
Endocr Relat Cancer. 2009 Sep;16(3):895-906. doi: 10.1677/ERC-09-0096. Epub 2009 Jun 22.
6
Investigation of key miRNAs and target genes in bladder cancer using miRNA profiling and bioinformatic tools.利用miRNA分析和生物信息学工具对膀胱癌中的关键miRNA和靶基因进行研究。
Mol Biol Rep. 2014 Dec;41(12):8127-35. doi: 10.1007/s11033-014-3713-5. Epub 2014 Sep 5.
7
Thyroid hormone may regulate mRNA abundance in liver by acting on microRNAs.甲状腺激素可能通过作用于 microRNAs 来调节肝脏中的 mRNA 丰度。
PLoS One. 2010 Aug 13;5(8):e12136. doi: 10.1371/journal.pone.0012136.
8
The Role of Significantly Deregulated MicroRNAs in Recurrent Cervical Cancer Based on Bioinformatic Analysis of the Cancer Genome Atlas Data.基于癌症基因组图谱数据的生物信息学分析探讨显著失调的微小RNA在复发性宫颈癌中的作用
J Comput Biol. 2019 Apr;26(4):387-395. doi: 10.1089/cmb.2018.0241. Epub 2019 Feb 14.
9
MicroRNA profiling of diabetic atherosclerosis in a rat model.糖尿病动脉粥样硬化大鼠模型的 microRNA 谱分析。
Eur J Med Res. 2018 Nov 3;23(1):55. doi: 10.1186/s40001-018-0354-5.
10
Differentially expressed microRNAs in the corpus cavernosum from a murine model with type 2 diabetes mellitus-associated erectile dysfunction.2型糖尿病相关性勃起功能障碍小鼠模型阴茎海绵体中差异表达的微小RNA
Mol Genet Genomics. 2016 Dec;291(6):2215-2224. doi: 10.1007/s00438-016-1250-8. Epub 2016 Sep 28.

本文引用的文献

1
The ability of microRNAs to regulate the immune response in ischemia/reperfusion inflammatory pathways.微小 RNA 调节缺血/再灌注炎症途径中免疫反应的能力。
Genes Immun. 2024 Aug;25(4):277-296. doi: 10.1038/s41435-024-00283-6. Epub 2024 Jun 22.
2
MicroRNA profiling in women with migraine: effects of CGRP-targeting treatment.偏头痛女性的 microRNA 谱分析:CGRP 靶向治疗的影响。
J Headache Pain. 2024 May 16;25(1):80. doi: 10.1186/s10194-024-01787-2.
3
DHT inhibits REDOX damage and neuroinflammation to reduce PND occurrence in aged mice via mmu_circ_0001442/miR-125a-3p/NUFIP2 axis.
双氢睾酮通过mmu_circ_0001442/miR-125a-3p/NUFIP2轴抑制氧化还原损伤和神经炎症,以减少老年小鼠产后神经功能障碍的发生。
Brain Behav. 2023 Oct;13(10):e3180. doi: 10.1002/brb3.3180. Epub 2023 Aug 7.
4
The Epigenetics of Migraine.偏头痛的表观遗传学。
Int J Mol Sci. 2023 May 23;24(11):9127. doi: 10.3390/ijms24119127.
5
PIM1 phosphorylates ABI2 to enhance actin dynamics and promote tumor invasion.PIM1 通过磷酸化 ABI2 来增强肌动蛋白动力学并促进肿瘤侵袭。
J Cell Biol. 2023 Jun 5;222(6). doi: 10.1083/jcb.202208136. Epub 2023 Apr 12.
6
A study of differential microRNA expression profile in migraine: the microMIG exploratory study.偏头痛差异 microRNA 表达谱研究: microMIG 探索性研究。
J Headache Pain. 2023 Feb 17;24(1):11. doi: 10.1186/s10194-023-01542-z.
7
Circulating exosomal microRNA profiles in migraine patients receiving acupuncture treatment: A placebo-controlled clinical trial.接受针灸治疗的偏头痛患者循环外泌体微小RNA谱:一项安慰剂对照临床试验。
Front Mol Neurosci. 2023 Jan 10;15:1098766. doi: 10.3389/fnmol.2022.1098766. eCollection 2022.
8
Elevation of hsa-miR-7-5p level mediated by CtBP1-p300-AP1 complex targets ATXN1 to trigger NF-κB-dependent inflammation response.由CtBP1-p300-AP1复合物介导的hsa-miR-7-5p水平升高靶向共济失调蛋白1(ATXN1),以触发核因子κB(NF-κB)依赖性炎症反应。
J Mol Med (Berl). 2023 Mar;101(3):223-235. doi: 10.1007/s00109-022-02274-4. Epub 2023 Jan 11.
9
Decreasing mutant ATXN1 nuclear localization improves a spectrum of SCA1-like phenotypes and brain region transcriptomic profiles.降低突变 ATXN1 的核定位可改善一系列 SCA1 样表型和大脑区域转录组图谱。
Neuron. 2023 Feb 15;111(4):493-507.e6. doi: 10.1016/j.neuron.2022.11.017. Epub 2022 Dec 27.
10
Membrane Atg8ylation, stress granule formation, and MTOR regulation during lysosomal damage.溶酶体损伤过程中的膜 Atg8 化、应激颗粒形成和 MTOR 调节。
Autophagy. 2023 Jun;19(6):1893-1895. doi: 10.1080/15548627.2022.2148900. Epub 2022 Nov 29.