• 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
Are Antisense Long Non-Coding RNA Related to COVID-19?反义长链非编码RNA与新型冠状病毒肺炎有关吗?
Biomedicines. 2022 Nov 1;10(11):2770. doi: 10.3390/biomedicines10112770.
2
lncRNA FLVCR1-AS1 regulates cell proliferation, migration and invasion by sponging miR-485-5p in human cholangiocarcinoma.长链非编码RNA FLVCR1-AS1通过海绵吸附miR-485-5p调控人胆管癌细胞的增殖、迁移和侵袭。
Oncol Lett. 2019 Sep;18(3):2240-2247. doi: 10.3892/ol.2019.10577. Epub 2019 Jul 5.
3
Long non-coding RNA FLVCR1-AS1 contributes to the proliferation and invasion of lung cancer by sponging miR-573 to upregulate the expression of E2F transcription factor 3.长链非编码 RNA FLVCR1-AS1 通过海绵吸附 miR-573 来上调 E2F 转录因子 3 的表达,促进肺癌的增殖和侵袭。
Biochem Biophys Res Commun. 2018 Nov 2;505(3):931-938. doi: 10.1016/j.bbrc.2018.09.057. Epub 2018 Oct 9.
4
Long non-coding RNA FLVCR1-AS1 sponges miR-155 to promote the tumorigenesis of gastric cancer by targeting c-Myc.长链非编码RNA FLVCR1-AS1通过靶向c-Myc海绵化miR-155以促进胃癌的肿瘤发生。
Am J Transl Res. 2019 Feb 15;11(2):793-805. eCollection 2019.
5
Long non-coding RNA FLVCR1-AS1 functions as a ceRNA to aggravate cervical cancer cell growth by the miR-381-3p/MAGT1 axis.长链非编码 RNA FLVCR1-AS1 通过 miR-381-3p/MAGT1 轴作为 ceRNA 加重宫颈癌细胞生长。
Arch Gynecol Obstet. 2022 Dec;306(6):2093-2103. doi: 10.1007/s00404-022-06468-6. Epub 2022 Apr 16.
6
Long noncoding RNA FLVCR1-AS1 aggravates biological behaviors of glioma cells via targeting miR-4731-5p/E2F2 axis.长链非编码 RNA FLVCR1-AS1 通过靶向 miR-4731-5p/E2F2 轴加重胶质瘤细胞的生物学行为。
Biochem Biophys Res Commun. 2020 Jan 15;521(3):716-720. doi: 10.1016/j.bbrc.2019.10.106. Epub 2019 Nov 5.
7
LncRNA FLVCR1-AS1 mediates miR-23a-5p/SLC7A11 axis to promote malignant behavior of cervical cancer cells.长链非编码 RNA FLVCR1-AS1 通过调控 miR-23a-5p/SLC7A11 轴促进宫颈癌的恶性行为。
Bioengineered. 2022 Apr;13(4):10454-10466. doi: 10.1080/21655979.2022.2059958.
8
LncRNA FLVCR1-AS1 mediates miR-513/YAP1 signaling to promote cell progression, migration, invasion and EMT process in ovarian cancer.长链非编码 RNA FLVCR1-AS1 通过调节 miR-513/YAP1 信号通路促进卵巢癌细胞的进展、迁移、侵袭和 EMT 过程。
J Exp Clin Cancer Res. 2019 Aug 14;38(1):356. doi: 10.1186/s13046-019-1356-z.
9
lncRNA FLVCR1-AS1 silencing inhibits lung cancer cell proliferation, migration, and invasion by inhibiting the activity of the Wnt/β-catenin signaling pathway.长链非编码RNA FLVCR1-AS1沉默通过抑制Wnt/β-连环蛋白信号通路的活性来抑制肺癌细胞的增殖、迁移和侵袭。
J Cell Biochem. 2019 Jun;120(6):10625-10632. doi: 10.1002/jcb.28352. Epub 2019 Jan 29.
10
LncRNA FLVCR1-AS1 acts as miR-513c sponge to modulate cancer cell proliferation, migration, and invasion in hepatocellular carcinoma.长链非编码 RNA FLVCR1-AS1 通过作为 miR-513c 的海绵体调节肝癌细胞的增殖、迁移和侵袭。
J Cell Biochem. 2018 Jul;119(7):6045-6056. doi: 10.1002/jcb.26802. Epub 2018 Mar 25.

引用本文的文献

1
Initial Evaluation of lncRNA A2M-AS1 Gene Expression in Multiple Sclerosis Patients.多发性硬化症患者中lncRNA A2M-AS1基因表达的初步评估
Adv Biomed Res. 2024 Sep 23;13:80. doi: 10.4103/abr.abr_422_23. eCollection 2024.
2
Challenges in LncRNA Biology: Views and Opinions.长链非编码RNA生物学中的挑战:观点与见解
Noncoding RNA. 2024 Aug 1;10(4):43. doi: 10.3390/ncrna10040043.
3
Long non-coding RNAs in biomarking COVID-19: a machine learning-based approach.基于机器学习的长非编码 RNA 在 COVID-19 生物标志物中的研究。
Virol J. 2024 Jun 7;21(1):134. doi: 10.1186/s12985-024-02408-9.
4
The regulation of lncRNAs and miRNAs in SARS-CoV-2 infection.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染中长链非编码RNA(lncRNAs)和微小RNA(miRNAs)的调控
Front Cell Dev Biol. 2023 Jul 27;11:1229393. doi: 10.3389/fcell.2023.1229393. eCollection 2023.
5
Computational identification of differentially-expressed genes as suggested novel COVID-19 biomarkers: A bioinformatics analysis of expression profiles.作为新型冠状病毒肺炎潜在生物标志物的差异表达基因的计算鉴定:表达谱的生物信息学分析
Comput Struct Biotechnol J. 2023;21:3339-3354. doi: 10.1016/j.csbj.2023.06.007. Epub 2023 Jun 12.
6
Dynamics of Gene Expression Profiling and Identification of High-Risk Patients for Severe COVID-19.新冠重症患者基因表达谱动态变化及高危患者的识别
Biomedicines. 2023 May 3;11(5):1348. doi: 10.3390/biomedicines11051348.
7
COVID-19: Mechanisms, risk factors, genetics, non-coding RNAs and neurologic impairments.新型冠状病毒肺炎:发病机制、风险因素、遗传学、非编码RNA与神经功能障碍
Noncoding RNA Res. 2023 Jun;8(2):240-254. doi: 10.1016/j.ncrna.2023.02.007. Epub 2023 Feb 23.

本文引用的文献

1
Materno-fetal iron transfer and the emerging role of ferroptosis pathways.母胎铁转运及铁死亡途径的新作用
Biochem Pharmacol. 2022 Aug;202:115141. doi: 10.1016/j.bcp.2022.115141. Epub 2022 Jun 12.
2
LncRNAs Target Ferroptosis-Related Genes and Impair Activation of CD4 T Cell in Gastric Cancer.长链非编码RNA靶向胃癌中与铁死亡相关的基因并损害CD4 T细胞的激活。
Front Cell Dev Biol. 2021 Dec 13;9:797339. doi: 10.3389/fcell.2021.797339. eCollection 2021.
3
The regulatory role of antisense lncRNAs in cancer.反义长链非编码RNA在癌症中的调控作用。
Cancer Cell Int. 2021 Aug 30;21(1):459. doi: 10.1186/s12935-021-02168-4.
4
Long Noncoding RNAs as Emerging Regulators of COVID-19.长链非编码 RNA 作为 COVID-19 的新兴调控因子。
Front Immunol. 2021 Aug 2;12:700184. doi: 10.3389/fimmu.2021.700184. eCollection 2021.
5
Ferroptosis in infection, inflammation, and immunity.铁死亡在感染、炎症和免疫中的作用。
J Exp Med. 2021 Jun 7;218(6). doi: 10.1084/jem.20210518. Epub 2021 May 12.
6
Risk stratification by long non-coding RNAs profiling in COVID-19 patients.基于长链非编码 RNA 特征分析的 COVID-19 患者风险分层。
J Cell Mol Med. 2021 May;25(10):4753-4764. doi: 10.1111/jcmm.16444. Epub 2021 Mar 23.
7
SARS-CoV infection crosstalk with human host cell noncoding-RNA machinery: An in-silico approach.SARS-CoV 感染与人类宿主细胞非编码 RNA 机制的串扰:一种计算机模拟方法。
Biomed Pharmacother. 2020 Oct;130:110548. doi: 10.1016/j.biopha.2020.110548. Epub 2020 Jul 28.
8
The Neat Dance of COVID-19: NEAT1, DANCR, and Co-Modulated Cholinergic RNAs Link to Inflammation.新冠病毒的精巧舞步:NEAT1、DANCR 及共调控胆碱能 RNA 与炎症相关联。
Front Immunol. 2020 Oct 9;11:590870. doi: 10.3389/fimmu.2020.590870. eCollection 2020.
9
Iron Metabolism in Ferroptosis.铁死亡中的铁代谢
Front Cell Dev Biol. 2020 Oct 7;8:590226. doi: 10.3389/fcell.2020.590226. eCollection 2020.
10
LncRNA A2M-AS1 lessens the injury of cardiomyocytes caused by hypoxia and reoxygenation via regulating IL1R2.长链非编码 RNA A2M-AS1 通过调节 IL1R2 减轻心肌细胞缺氧/复氧损伤。
Genes Genomics. 2020 Dec;42(12):1431-1441. doi: 10.1007/s13258-020-01007-6. Epub 2020 Oct 14.

反义长链非编码RNA与新型冠状病毒肺炎有关吗?

Are Antisense Long Non-Coding RNA Related to COVID-19?

作者信息

Badr Eman Ae, El Sayed Ibrahim Eltantawy, Gabber Mohanad Kareem Razak, Ghobashy Eman Abd Elrehem, Al-Sehemi Abdullah G, Algarni Hamed, Elghobashy Yasser As

机构信息

Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Menoufia University, Shebeen El-Kom 32511, Egypt.

Department of Chemistry, Faculty of Science, Menoufia University, Shebeen El-Kom 32511, Egypt.

出版信息

Biomedicines. 2022 Nov 1;10(11):2770. doi: 10.3390/biomedicines10112770.

DOI:10.3390/biomedicines10112770
PMID:36359290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9687826/
Abstract

Fighting external pathogens relies on the tight regulation of the gene expression of the immune system. Ferroptosis, which is a distinct form of programmed cell death driven by iron, is involved in the enhancement of follicular helper T cell function during infection. The regulation of RNA is a key step in final gene expression. The present study aimed to identify the expression level of antisense lncRNAs (A2M-AS1, DBH-AS1, FLVCR1-DT, and NCBP2AS2-1) and FLVCR1 in COVID-19 patients and its relation to the severity of the disease. COVID-19 patients as well as age and gender-matched healthy controls were enrolled in this study. The expression level of the antisense lncRNAs was measured by RT-PCR. Results revealed the decreased expression of A2M-AS1 and FLVCR1 in COVID-19 patients. Additionally, they showed the increased expression of DBH-AS1, FLVCR1-DT, and NCBP2AS2. Both FLVCR1-DT and NCBP2AS2 showed a positive correlation with interleukin-6 (IL-6). DBH-AS1 and FLVCR1-DT had a significant association with mortality, complications, and mechanical ventilation. A significant negative correlation was found between A2M-AS1 and NCBP2AS2-1 and between FLVCR1 and FLVCR1-DT. The study confirmed that the expression level of the antisense lncRNAs was deregulated in COVID-19 patients and correlated with the severity of COVID-19, and that it may have possible roles in the pathogenesis of this disease.

摘要

抵御外部病原体依赖于免疫系统基因表达的严格调控。铁死亡是一种由铁驱动的独特程序性细胞死亡形式,参与感染期间滤泡辅助性T细胞功能的增强。RNA的调控是最终基因表达的关键步骤。本研究旨在确定COVID-19患者中反义长链非编码RNA(A2M-AS1、DBH-AS1、FLVCR1-DT和NCBP2AS2-1)和FLVCR1的表达水平及其与疾病严重程度的关系。本研究纳入了COVID-19患者以及年龄和性别匹配的健康对照。通过逆转录聚合酶链反应(RT-PCR)测量反义长链非编码RNA的表达水平。结果显示,COVID-19患者中A2M-AS1和FLVCR1的表达降低。此外,他们还显示DBH-AS1、FLVCR1-DT和NCBP2AS2的表达增加。FLVCR1-DT和NCBP2AS2均与白细胞介素-6(IL-6)呈正相关。DBH-AS1和FLVCR1-DT与死亡率、并发症和机械通气有显著关联。在A2M-AS1与NCBP2AS2-1之间以及FLVCR1与FLVCR1-DT之间发现显著负相关。该研究证实,COVID-19患者中反义长链非编码RNA的表达水平失调,与COVID-19的严重程度相关,并且可能在该疾病的发病机制中发挥作用。