• 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

基于共表达网络的脊髓损伤相关微小RNA的鉴定

Identification of disease-related miRNAs based on co-expression network in spinal cord injury.

作者信息

Xing Shun Min, Wang Jinxin, He Xiang, Lai Jin, Shen Lianbing, Chen Dechun, Fu Kai, Tan Junming

机构信息

1Department of Orthopedics, the 98nd Hospital of PLA, Huzhou.

出版信息

Int J Neurosci. 2015 Apr;125(4):270-6. doi: 10.3109/00207454.2014.930741. Epub 2014 Jul 14.

DOI:10.3109/00207454.2014.930741
PMID:24946205
Abstract

OBJECTIVE

This study aimed to construct miRNA co-expression network by using miRNA microarray data and screen the miRNAs associated with spinal cord injury (SCI) by comparative analysis, which might be considered as molecule labels for future forecasts or therapies.

METHODS

We first downloaded SCI gene expression data GSE19890 from GEO (Gene Expression Omnibus), then constructed the miRNA co-expression network under three different states and analyzed the topologic attributes of network. After that, miRNAs associated with SCI were screened and subjected to function analysis by DAVID (Database for Annotation, Visualization and Integrated Discovery).

RESULTS

In the co-expression network, miR-520a and miR-193b had the largest degree in the SCI and sham groups, respectively. A total of 22 differentially expressed miRNAs were identified. MiR-32 and miR-471 were the most significantly expressed in the SCI group compared with control and sham groups, respectively, which were newly reported to be related to SCI in this study. Function enrichment analysis of the target genes indicated that the screened miRNA were associated with cell adhesion, cytoplasmic vesicle and so on.

CONCLUSIONS

MiRNAs identified in this study could be considered targets for SCI diagnosis and therapy.

摘要

目的

本研究旨在利用 miRNA 微阵列数据构建 miRNA 共表达网络,并通过比较分析筛选出与脊髓损伤(SCI)相关的 miRNAs,这些 miRNAs 可被视为未来预测或治疗的分子标记。

方法

我们首先从 GEO(基因表达综合数据库)下载 SCI 基因表达数据 GSE19890,然后构建三种不同状态下的 miRNA 共表达网络并分析网络的拓扑属性。之后,筛选出与 SCI 相关的 miRNAs,并通过 DAVID(注释、可视化和综合发现数据库)进行功能分析。

结果

在共表达网络中,miR-520a 和 miR-193b 分别在 SCI 组和假手术组中具有最大的度值。共鉴定出 22 个差异表达的 miRNAs。与对照组和假手术组相比,miR-32 和 miR-471 分别在 SCI 组中表达最为显著,本研究首次报道它们与 SCI 相关。对靶基因的功能富集分析表明,筛选出的 miRNA 与细胞黏附、细胞质囊泡等相关。

结论

本研究中鉴定出的 miRNAs 可被视为 SCI 诊断和治疗的靶点。

相似文献

1
Identification of disease-related miRNAs based on co-expression network in spinal cord injury.基于共表达网络的脊髓损伤相关微小RNA的鉴定
Int J Neurosci. 2015 Apr;125(4):270-6. doi: 10.3109/00207454.2014.930741. Epub 2014 Jul 14.
2
Bioinformatics Analysis of microRNA Time-Course Expression in Brown Rat (Rattus norvegicus): Spinal Cord Injury Self-Repair.棕色大鼠(褐家鼠)脊髓损伤自我修复过程中微小RNA时间进程表达的生物信息学分析
Spine (Phila Pa 1976). 2016 Jan;41(2):97-103. doi: 10.1097/BRS.0000000000001323.
3
Integrated analysis of competing endogenous RNA (ceRNA) networks in subacute stage of spinal cord injury.脊髓损伤亚急性期竞争性内源性 RNA(ceRNA)网络的综合分析。
Gene. 2020 Feb 5;726:144171. doi: 10.1016/j.gene.2019.144171. Epub 2019 Oct 26.
4
Regulation of gene expression in rats with spinal cord injury based on microarray data.基于微阵列数据的大鼠脊髓损伤基因表达调控
Mol Med Rep. 2015 Aug;12(2):2465-72. doi: 10.3892/mmr.2015.3670. Epub 2015 Apr 23.
5
Screening miRNA and their target genes related to tetralogy of Fallot with microarray.用微阵列筛选与法洛四联症相关的微小RNA及其靶基因。
Cardiol Young. 2014 Jun;24(3):442-6. doi: 10.1017/S104795111300053X. Epub 2013 May 17.
6
Bioinformatic Analysis of Potential microRNAs in Ischemic Stroke.缺血性中风中潜在微小RNA的生物信息学分析
J Stroke Cerebrovasc Dis. 2016 Jul;25(7):1753-1759. doi: 10.1016/j.jstrokecerebrovasdis.2016.03.023. Epub 2016 Apr 14.
7
MAP‑1B, PACS‑2 and AHCYL1 are regulated by miR‑34A/B/C and miR‑449 in neuroplasticity following traumatic spinal cord injury in rats: Preliminary explorative results from microarray data.MAP-1B、PACS-2 和 AHCYL1 在大鼠创伤性脊髓损伤后的神经重塑中受 miR-34A/B/C 和 miR-449 的调控:来自微阵列数据的初步探索性结果。
Mol Med Rep. 2019 Oct;20(4):3011-3018. doi: 10.3892/mmr.2019.10538. Epub 2019 Jul 30.
8
MicroRNA expression profiling and functional annotation analysis of their targets associated with the malignant transformation of oral leukoplakia.与口腔白斑恶变相关的微小RNA表达谱及其靶标的功能注释分析
Gene. 2015 Mar 10;558(2):271-7. doi: 10.1016/j.gene.2015.01.004. Epub 2015 Jan 6.
9
Uncovering the shared neuro-immune-related regulatory mechanisms between spinal cord injury and osteoarthritis.揭示脊髓损伤与骨关节炎之间共享的神经免疫相关调节机制。
Heliyon. 2024 Apr 25;10(9):e30336. doi: 10.1016/j.heliyon.2024.e30336. eCollection 2024 May 15.
10
Bioinformatic Analysis of Potential Biomarkers for Spinal Cord-injured Patients with Intractable Neuropathic Pain.生物信息学分析脊髓损伤伴难治性神经病理性疼痛患者的潜在生物标志物。
Clin J Pain. 2018 Sep;34(9):825-830. doi: 10.1097/AJP.0000000000000608.

引用本文的文献

1
Analysis and experimental validation of genes and their transcription factor prediction in contused rat spinal cord at the intermediate phase.分析和实验验证在中间阶段挫伤的大鼠脊髓中的基因及其转录因子的预测。
Aging (Albany NY). 2024 Jun 8;16(11):9990-10003. doi: 10.18632/aging.205912.
2
MicroRNA-145-Mediated KDM6A Downregulation Enhances Neural Repair after Spinal Cord Injury the NOTCH2/Abcb1a Axis.miRNA-145 介导的 KDM6A 下调增强脊髓损伤后的神经修复——NOTCH2/Abcb1a 轴。
Oxid Med Cell Longev. 2021 May 25;2021:2580619. doi: 10.1155/2021/2580619. eCollection 2021.
3
Comprehensive analysis of the differential expression profile of microRNAs in rats with spinal cord injury treated by electroacupuncture.
电针对脊髓损伤大鼠差异表达 microRNAs 的综合分析。
Mol Med Rep. 2020 Aug;22(2):751-762. doi: 10.3892/mmr.2020.11161. Epub 2020 May 20.
4
Extrinsic and Intrinsic Regulation of Axon Regeneration by MicroRNAs after Spinal Cord Injury.脊髓损伤后微小RNA对轴突再生的外在和内在调节
Neural Plast. 2016;2016:1279051. doi: 10.1155/2016/1279051. Epub 2016 Oct 13.