• 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

miR-155 的表达增加与实体器官移植受者和大鼠肾移植模型中的异常移植物状态相关。

Increased expression of miR-155 correlates with abnormal allograft status in solid organ transplant patients and rat kidney transplantation model.

机构信息

Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.

Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

Life Sci. 2019 Jun 15;227:51-57. doi: 10.1016/j.lfs.2019.04.043. Epub 2019 Apr 17.

DOI:10.1016/j.lfs.2019.04.043
PMID:31004655
Abstract

AIMS

Increasing evidence has shown the diagnostic value of miR-155 in organ transplantation. The dysregulation of miR-155 is reported to be associated with development of acute or chronic complications in solid organ transplant recipients. Here, we summarized related evidence to explore the correlation between the dysregulation of miR-155 and various allograft dysfunction in transplant recipients, and verified the dynamic change of miR-155 level in acute rejection (AR) using a rat renal transplantation model.

MAIN METHODS

Eligible studies were retrieved from PubMed, Embase, and Cochrane Library databases. A meta-analysis method was performed to evaluate the diagnostic value of miR-155 in transplant recipients. Furthermore, the F344-Lewis rat renal transplantation model was established to validate the dynamic change of miR-155 expression during AR.

KEY FINDINGS

A total of 275 transplant patients, including renal, heart, and lung transplantation from 6 studies were analysed. The pooled SEN of miR-155 was 0.87 (95% CI, 0.78-0.93), the pooled SPE was 0.76 (95% CI, 0.63-0.85), the pooled PLR was 3.6 (95% CI, 2.2-5.8), the pooled NLR was 0.17 (95% CI, 0.09-0.31), the pooled DOR was 17.31 (95% CI, 7.20-41.65) and pooled AUC was 0.89 (95% CI, 0.86-0.92). The rat renal transplantation model (n = 24) and control model (n = 15) were successfully established. Expression of miR-155 in plasma was significantly increased in 7 d and 9 d post-transplantation compared to the control group (P < 0.05), and was consistent with the dynamic change of AR degree.

SIGNIFICANCE

miR-155 is a potential biomarker for monitoring the abnormal allograft status in solid organ transplantation.

摘要

目的

越来越多的证据表明 miR-155 在器官移植中的诊断价值。据报道,miR-155 的失调与实体器官移植受者急性或慢性并发症的发展有关。在这里,我们总结了相关证据,探讨了 miR-155 失调与移植受者各种同种异体移植物功能障碍之间的相关性,并通过大鼠肾移植模型验证了 miR-155 水平在急性排斥反应 (AR) 中的动态变化。

主要方法

从 PubMed、Embase 和 Cochrane Library 数据库中检索符合条件的研究。采用荟萃分析方法评估 miR-155 在移植受者中的诊断价值。此外,建立了 F344-Lewis 大鼠肾移植模型,以验证 AR 期间 miR-155 表达的动态变化。

主要发现

共分析了 6 项研究中的 275 例肾、心和肺移植患者。miR-155 的汇总 SEN 为 0.87(95%CI,0.78-0.93),汇总 SPE 为 0.76(95%CI,0.63-0.85),汇总 PLR 为 3.6(95%CI,2.2-5.8),汇总 NLR 为 0.17(95%CI,0.09-0.31),汇总 DOR 为 17.31(95%CI,7.20-41.65),汇总 AUC 为 0.89(95%CI,0.86-0.92)。成功建立了大鼠肾移植模型(n=24)和对照组模型(n=15)。与对照组相比,移植后 7d 和 9d 血浆中 miR-155 的表达显著增加(P<0.05),与 AR 程度的动态变化一致。

意义

miR-155 是监测实体器官移植中同种异体移植物异常状态的潜在生物标志物。

相似文献

1
Increased expression of miR-155 correlates with abnormal allograft status in solid organ transplant patients and rat kidney transplantation model.miR-155 的表达增加与实体器官移植受者和大鼠肾移植模型中的异常移植物状态相关。
Life Sci. 2019 Jun 15;227:51-57. doi: 10.1016/j.lfs.2019.04.043. Epub 2019 Apr 17.
2
Plasma microRNA, a potential biomarker for acute rejection after liver transplantation.血浆 microRNA:肝移植后急性排斥反应的潜在生物标志物
Transplantation. 2013 Apr 27;95(8):991-9. doi: 10.1097/TP.0b013e31828618d8.
3
Circulating miR-150, miR-192, miR-200b, and miR-423-3p as Non-invasive Biomarkers of Chronic Allograft Dysfunction.循环 miR-150、miR-192、miR-200b 和 miR-423-3p 作为慢性移植物功能障碍的非侵入性生物标志物。
Arch Med Res. 2017 Jan;48(1):96-104. doi: 10.1016/j.arcmed.2017.03.004.
4
MicroRNAs as non-invasive biomarkers of heart transplant rejection.微小 RNA 作为心脏移植排斥的非侵入性生物标志物。
Eur Heart J. 2014 Dec 1;35(45):3194-202. doi: 10.1093/eurheartj/ehu346. Epub 2014 Aug 31.
5
FK778, a powerful new immunosuppressant, effectively reduces functional and histologic changes of chronic rejection in rat renal allografts.FK778是一种强效新型免疫抑制剂,可有效减轻大鼠肾移植慢性排斥反应的功能和组织学变化。
Transplantation. 2003 Apr 27;75(8):1110-4. doi: 10.1097/01.TP.0000063704.19149.E3.
6
Serum Levels of miR-155, miR-326, and miR-133b as Early Diagnostic Biomarkers for the Detection of Human Acute Heart Allograft Rejection in Comparison with Serum Cardiac Troponin T.与血清心肌肌钙蛋白T相比,血清miR-155、miR-326和miR-133b水平作为检测人类心脏同种异体移植急性排斥反应的早期诊断生物标志物
Heart Surg Forum. 2018 Mar 12;21(2):E101-E107. doi: 10.1532/hsf.1887.
7
Antibody response against perlecan and collagen types IV and VI in chronic renal allograft rejection in the rat.大鼠慢性肾移植排斥反应中针对基底膜聚糖、IV型和VI型胶原的抗体反应
Am J Pathol. 2002 Apr;160(4):1301-10. doi: 10.1016/S0002-9440(10)62557-6.
8
Essential role of microRNA-650 in the regulation of B-cell CLL/lymphoma 11B gene expression following transplantation: A novel mechanism behind the acute rejection of renal allografts.miR-650 在移植后调控 B 细胞慢性淋巴细胞白血病/淋巴瘤 11B 基因表达中的重要作用:同种异体肾移植急性排斥反应的新机制。
Int J Mol Med. 2017 Dec;40(6):1840-1850. doi: 10.3892/ijmm.2017.3194. Epub 2017 Oct 17.
9
Diagnostic Performance of Fas Ligand mRNA Expression for Acute Rejection after Kidney Transplantation: A Systematic Review and Meta-Analysis.肾移植后急性排斥反应中Fas配体mRNA表达的诊断性能:一项系统评价和荟萃分析
PLoS One. 2016 Nov 3;11(11):e0165628. doi: 10.1371/journal.pone.0165628. eCollection 2016.
10
PG490-88, a new immunosuppressant, effectively prevents acute and chronic rejection in rat renal allografts.新型免疫抑制剂PG490-88可有效预防大鼠肾移植中的急性和慢性排斥反应。
Transplant Proc. 2005 Jan-Feb;37(1):134-6. doi: 10.1016/j.transproceed.2004.12.054.

引用本文的文献

1
Epigenetic Regulation in Kidney Transplantation.肾移植中的表观遗传调控。
Front Immunol. 2022 Apr 8;13:861498. doi: 10.3389/fimmu.2022.861498. eCollection 2022.
2
KLF4 Affects Acute Renal Allograft Injury via Binding to MicroRNA-155-5p Promoter to Regulate ERRFI1.KLF4 通过与 microRNA-155-5p 启动子结合调控 ERRFI1 影响急性肾移植损伤。
Dis Markers. 2022 Mar 17;2022:5845627. doi: 10.1155/2022/5845627. eCollection 2022.
3
Multi-omics network characterization reveals novel microRNA biomarkers and mechanisms for diagnosis and subtyping of kidney transplant rejection.
多组学网络特征分析揭示了新型 miRNA 生物标志物及其在肾移植排斥诊断和分型中的作用机制。
J Transl Med. 2021 Aug 13;19(1):346. doi: 10.1186/s12967-021-03025-8.
4
MicroRNAs as theranostic markers in cardiac allograft transplantation: from murine models to clinical practice.微小RNA作为心脏同种异体移植中的诊疗标志物:从鼠类模型到临床实践
Theranostics. 2021 Apr 7;11(12):6058-6073. doi: 10.7150/thno.56327. eCollection 2021.
5
Screening and identification of key regulatory connections and immune cell infiltration characteristics for lung transplant rejection using mucosal biopsies.使用黏膜活检筛选和鉴定肺移植排斥反应的关键调控关联及免疫细胞浸润特征。
Int Immunopharmacol. 2020 Oct;87:106827. doi: 10.1016/j.intimp.2020.106827. Epub 2020 Aug 10.