• 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

MALAT-1、NEAT-1、THRIL 和 miR-155-5p 在 COVID-19 疾病的急性期到亚急性期的表达模式。

The expression patterns of MALAT-1, NEAT-1, THRIL, and miR-155-5p in the acute to the post-acute phase of COVID-19 disease.

机构信息

Iran University of Medical Sciences, Deputy of Health, Tehran, Iran.

Tabriz University of Medical Sciences, Infectious and Tropical Diseases Research Center, Tabriz, Iran.

出版信息

Braz J Infect Dis. 2022 May-Jun;26(3):102354. doi: 10.1016/j.bjid.2022.102354. Epub 2022 Apr 25.

DOI:10.1016/j.bjid.2022.102354
PMID:35500644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9035361/
Abstract

INTRODUCTION

One of the hallmarks of COVID-19 is overwhelming inflammation, which plays a very important role in the pathogenesis of COVID-19. Thus, identification of inflammatory factors that interact with the SARS-CoV-2 can be very important to control and diagnose the severity of COVID-19. The aim of this study was to investigate the expression patterns of inflammation-related non-coding RNAs (ncRNAs) including MALAT-1, NEAT-1, THRIL, and miR-155-5p from the acute phase to the recovery phase of COVID-19.

METHODS

Total RNA was extracted from Peripheral Blood Mononuclear Cell (PBMC) samples of 20 patients with acute COVID-19 infection and 20 healthy individuals and the expression levels of MALAT-1, NEAT-1, THRIL, and miR-155-5p were evaluated by real-time PCR assay. Besides, in order to monitor the expression pattern of selected ncRNAs from the acute phase to the recovery phase of COVID-19 disease, the levels of ncRNAs were re-measured 6‒7 weeks after the acute phase.

RESULT

The mean expression levels of MALAT-1, THRIL, and miR-155-5p were significantly increased in the acute phase of COVID-19 compared with a healthy control group. In addition, the expression levels of MALAT-1 and THRIL in the post-acute phase of COVID-19 were significantly lower than in the acute phase of COVID-19. According to the ROC curve analysis, these ncRNAs could be considered useful biomarkers for COVID-19 diagnosis and for discriminating between acute and post-acute phase of COVID-19.

DISCUSSION

Inflammation-related ncRNAs (MALAT-1, THRIL, and miR-150-5p) can act as hopeful biomarkers for the monitoring and diagnosis of COVID-19 disease.

摘要

简介

COVID-19 的一个特征是炎症的压倒性反应,这在 COVID-19 的发病机制中起着非常重要的作用。因此,鉴定与 SARS-CoV-2 相互作用的炎症因子对于控制和诊断 COVID-19 的严重程度非常重要。本研究旨在从急性到恢复期 COVID-19 调查炎症相关非编码 RNA(ncRNA)包括 MALAT-1、NEAT-1、THRIL 和 miR-155-5p 的表达模式。

方法

从 20 名急性 COVID-19 感染患者和 20 名健康个体的外周血单核细胞(PBMC)样本中提取总 RNA,并通过实时 PCR 检测 MALAT-1、NEAT-1、THRIL 和 miR-155-5p 的表达水平。此外,为了监测 COVID-19 疾病急性到恢复期选定 ncRNA 的表达模式,在急性后 6-7 周重新测量 ncRNA 的水平。

结果

与健康对照组相比,COVID-19 急性期中 MALAT-1、THRIL 和 miR-155-5p 的平均表达水平显着升高。此外,COVID-19 急性后期中 MALAT-1 和 THRIL 的表达水平显着低于急性期中的表达水平。根据 ROC 曲线分析,这些 ncRNA 可被视为 COVID-19 诊断和区分急性和急性后 COVID-19 的有用生物标志物。

讨论

炎症相关 ncRNA(MALAT-1、THRIL 和 miR-155-5p)可作为监测和诊断 COVID-19 疾病的有希望的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494c/9387450/0b18554dd6fa/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494c/9387450/5c0da4262b5b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494c/9387450/cbc7dc0824a2/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494c/9387450/0b18554dd6fa/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494c/9387450/5c0da4262b5b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494c/9387450/cbc7dc0824a2/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/494c/9387450/0b18554dd6fa/gr3.jpg

相似文献

1
The expression patterns of MALAT-1, NEAT-1, THRIL, and miR-155-5p in the acute to the post-acute phase of COVID-19 disease.MALAT-1、NEAT-1、THRIL 和 miR-155-5p 在 COVID-19 疾病的急性期到亚急性期的表达模式。
Braz J Infect Dis. 2022 May-Jun;26(3):102354. doi: 10.1016/j.bjid.2022.102354. Epub 2022 Apr 25.
2
Acute and post-acute phase of COVID-19: Analyzing expression patterns of miRNA-29a-3p, 146a-3p, 155-5p, and let-7b-3p in PBMC.新型冠状病毒肺炎的急性期和恢复期:分析 PBMC 中 miRNA-29a-3p、146a-3p、155-5p 和 let-7b-3p 的表达模式。
Int Immunopharmacol. 2021 Aug;97:107641. doi: 10.1016/j.intimp.2021.107641. Epub 2021 Apr 6.
3
Long non-coding RNAs ANRIL, THRIL, and NEAT1 as potential circulating biomarkers of SARS-CoV-2 infection and disease severity.长链非编码 RNA ANRIL、THRIL 和 NEAT1 作为 SARS-CoV-2 感染和疾病严重程度的潜在循环生物标志物。
Virus Res. 2023 Oct 15;336:199214. doi: 10.1016/j.virusres.2023.199214. Epub 2023 Sep 11.
4
Inter-correlation of lncRNA THRIL with microRNA-34a and microRNA-125b and their relationship with childhood asthma risk, severity, and inflammation.长链非编码RNA THRIL与微小RNA-34a和微小RNA-125b的相互关联及其与儿童哮喘风险、严重程度和炎症的关系。
Allergol Immunopathol (Madr). 2023 Jan 1;51(1):187-194. doi: 10.15586/aei.v51i1.736. eCollection 2023.
5
LncRNA MALAT-1 regulates the growth of interleukin-22-stimulated keratinocytes via the miR-330-5p/S100A7 axis.长链非编码 RNA MALAT-1 通过 miR-330-5p/S100A7 轴调节白细胞介素-22 刺激的角质形成细胞的生长。
Autoimmunity. 2022 Feb;55(1):32-42. doi: 10.1080/08916934.2021.2001802. Epub 2021 Nov 11.
6
Long non-coding RNA THRIL promotes LPS-induced inflammatory injury by down-regulating microRNA-125b in ATDC5 cells.长非编码 RNA THRIL 通过下调 ATDC5 细胞中的 microRNA-125b 促进 LPS 诱导的炎症损伤。
Int Immunopharmacol. 2019 Jan;66:354-361. doi: 10.1016/j.intimp.2018.11.038. Epub 2018 Dec 4.
7
Elevated miR-182-5p Associates with Renal Cancer Cell Mitotic Arrest through Diminished Expression.miR-182-5p 升高通过降低表达与肾癌细胞有丝分裂阻滞相关。
Mol Cancer Res. 2018 Nov;16(11):1750-1760. doi: 10.1158/1541-7786.MCR-17-0762. Epub 2018 Jul 23.
8
Pivotal role of long non-coding ribonucleic acid-X-inactive specific transcript in regulating immune checkpoint programmed death ligand 1 through a shared pathway between miR-194-5p and miR-155-5p in hepatocellular carcinoma.长链非编码核糖核酸X染色体失活特异性转录本在肝细胞癌中通过miR-194-5p和miR-155-5p的共享途径调控免疫检查点程序性死亡配体1中的关键作用
World J Hepatol. 2020 Dec 27;12(12):1211-1227. doi: 10.4254/wjh.v12.i12.1211.
9
Analyzing the expression pattern of the noncoding RNAs (HOTAIR, PVT-1, XIST, H19, and miRNA-34a) in PBMC samples of patients with COVID-19, according to the disease severity in Iran during 2022-2023: A cross-sectional study.根据2022 - 2023年伊朗COVID - 19患者疾病严重程度,分析COVID - 19患者外周血单个核细胞(PBMC)样本中非编码RNA(HOTAIR、PVT - 1、XIST、H19和miRNA - 34a)的表达模式:一项横断面研究。
Health Sci Rep. 2024 Feb 7;7(2):e1861. doi: 10.1002/hsr2.1861. eCollection 2024 Feb.
10
Whole-Transcriptome RNA Sequencing Reveals Significant Differentially Expressed mRNAs, miRNAs, and lncRNAs and Related Regulating Biological Pathways in the Peripheral Blood of COVID-19 Patients.全转录组 RNA 测序揭示了 COVID-19 患者外周血中显著差异表达的 mRNAs、miRNAs 和 lncRNAs 及相关调控的生物学通路。
Mediators Inflamm. 2021 Apr 1;2021:6635925. doi: 10.1155/2021/6635925. eCollection 2021.

引用本文的文献

1
Ferroptosis and non-coding RNAs in breast cancer: insights into CAF and TAM interactions.乳腺癌中的铁死亡与非编码RNA:对癌症相关成纤维细胞和肿瘤相关巨噬细胞相互作用的见解
Discov Oncol. 2025 Aug 31;16(1):1658. doi: 10.1007/s12672-025-03507-x.
2
Expression Profile of Serum CircFUNDC1 and CircUHRF1 Can Differentiate Between Colorectal Cancer and Inflammatory Bowel Diseases (Ulcerative Colitis and Crohn's Disease).血清CircFUNDC1和CircUHRF1的表达谱可区分结直肠癌与炎症性肠病(溃疡性结肠炎和克罗恩病)。
J Clin Lab Anal. 2025 Jun;39(11):e70039. doi: 10.1002/jcla.70039. Epub 2025 May 16.
3
Exosomal non-coding RNAs: gatekeepers of inflammation in autoimmune disease.

本文引用的文献

1
Long non-coding RNAs (lncRNAs) NEAT1 and MALAT1 are differentially expressed in severe COVID-19 patients: An integrated single-cell analysis.长链非编码 RNA(lncRNA)NEAT1 和 MALAT1 在重症 COVID-19 患者中表达差异:一项综合单细胞分析。
PLoS One. 2022 Jan 10;17(1):e0261242. doi: 10.1371/journal.pone.0261242. eCollection 2022.
2
MicroRNA-155 and antiviral immune responses.miRNA-155 与抗病毒免疫反应
Int Immunopharmacol. 2021 Dec;101(Pt A):108188. doi: 10.1016/j.intimp.2021.108188. Epub 2021 Oct 6.
3
Non-Coding RNAs: Master Regulators of Inflammasomes in Inflammatory Diseases.
外泌体非编码RNA:自身免疫性疾病炎症的守门人。
J Inflamm (Lond). 2025 May 14;22(1):18. doi: 10.1186/s12950-025-00443-z.
4
To be or not to be: navigating the influence of MicroRNAs on cervical cancer cell death.存在还是不存在:探究微小RNA对宫颈癌细胞死亡的影响
Cancer Cell Int. 2025 Apr 18;25(1):153. doi: 10.1186/s12935-025-03786-y.
5
Harnessing Epigenetics: Innovative Approaches in Diagnosing and Combating Viral Acute Respiratory Infections.利用表观遗传学:诊断和对抗病毒性急性呼吸道感染的创新方法。
Pathogens. 2025 Feb 1;14(2):129. doi: 10.3390/pathogens14020129.
6
Peripheral lncRNA NEAT-1, miR374b-5p, and IL6 panel to guide in COVID-19 patients' diagnosis and prognosis.外周lncRNA NEAT-1、miR374b-5p和IL6检测指标用于指导COVID-19患者的诊断和预后。
PLoS One. 2024 Dec 27;19(12):e0313042. doi: 10.1371/journal.pone.0313042. eCollection 2024.
7
Bile's Hidden Weapon: Modulating the Microbiome and Tumor Microenvironment.胆汁的隐藏武器:调节微生物组和肿瘤微环境。
Curr Microbiol. 2024 Nov 30;82(1):25. doi: 10.1007/s00284-024-04004-0.
8
Regulatory role of microRNAs in virus-mediated inflammation.微小RNA在病毒介导的炎症中的调节作用。
J Inflamm (Lond). 2024 Nov 4;21(1):43. doi: 10.1186/s12950-024-00417-7.
9
Expression pattern analysis of the long non-coding RNAs (TINCR, RP11-573D15.8, RP11-156E8.1), and their target genes (AKT1, FOXO1 and MAPK3) in patients with HIV infection, and elite controllers.人类免疫缺陷病毒(HIV)感染者及精英控制者中长链非编码RNA(TINCR、RP11-573D15.8、RP11-156E8.1)及其靶基因(AKT1、FOXO1和MAPK3)的表达模式分析
Heliyon. 2024 May 10;10(10):e30900. doi: 10.1016/j.heliyon.2024.e30900. eCollection 2024 May 30.
10
Beyond acute infection: molecular mechanisms underpinning cardiovascular complications in long COVID.超越急性感染:长期新冠心血管并发症的分子机制
Front Cardiovasc Med. 2024 Feb 14;11:1268571. doi: 10.3389/fcvm.2024.1268571. eCollection 2024.
非编码RNA:炎症性疾病中炎性小体的主要调节因子
J Inflamm Res. 2021 Sep 30;14:5023-5050. doi: 10.2147/JIR.S332840. eCollection 2021.
4
Non-Coding RNAs in COVID-19: Emerging Insights and Current Questions.新型冠状病毒肺炎中的非编码RNA:新见解与当前问题
Noncoding RNA. 2021 Aug 31;7(3):54. doi: 10.3390/ncrna7030054.
5
NEAT1 and MALAT1 are highly expressed in saliva and nasopharyngeal swab samples of COVID-19 patients.NEAT1 和 MALAT1 在 COVID-19 患者的唾液和鼻咽拭子样本中高表达。
Mol Oral Microbiol. 2021 Dec;36(6):291-294. doi: 10.1111/omi.12351. Epub 2021 Sep 8.
6
Nuclear factor-kappa B and its role in inflammatory lung disease.核因子-κB 及其在炎症性肺疾病中的作用。
Chem Biol Interact. 2021 Aug 25;345:109568. doi: 10.1016/j.cbi.2021.109568. Epub 2021 Jun 25.
7
Striking absence of "usual suspects" during the winter of the coronavirus disease 2019 (COVID-19) pandemic 2020-2021.在2020 - 2021年冠状病毒病(COVID - 19)大流行的冬季,“常见病原体”明显缺失。
Infect Control Hosp Epidemiol. 2021 Dec;42(12):1516-1517. doi: 10.1017/ice.2021.303. Epub 2021 Jun 24.
8
Acute and post-acute phase of COVID-19: Analyzing expression patterns of miRNA-29a-3p, 146a-3p, 155-5p, and let-7b-3p in PBMC.新型冠状病毒肺炎的急性期和恢复期:分析 PBMC 中 miRNA-29a-3p、146a-3p、155-5p 和 let-7b-3p 的表达模式。
Int Immunopharmacol. 2021 Aug;97:107641. doi: 10.1016/j.intimp.2021.107641. Epub 2021 Apr 6.
9
The pro-inflammatory microRNA miR-155 influences fibrillar β-Amyloid catabolism by microglia.促炎 microRNA miR-155 通过小胶质细胞影响纤维状 β-淀粉样蛋白的代谢。
Glia. 2021 Jul;69(7):1736-1748. doi: 10.1002/glia.23988. Epub 2021 Mar 10.
10
Long non-coding RNA THRIL inhibits miRNA-24-3p to upregulate neuropilin-1 to aggravate cerebral ischemia-reperfusion injury through regulating the nuclear factor κB p65 signaling.长链非编码 RNA THRIL 通过调节核因子 κB p65 信号通路抑制 miRNA-24-3p 上调神经纤毛蛋白-1 加重脑缺血再灌注损伤。
Aging (Albany NY). 2021 Mar 6;13(6):9071-9084. doi: 10.18632/aging.202762.