Evaluation of the Expression of Infection-Related Long Noncoding RNAs among COVID-19 Patients: A Case-Control Study

IF 1.4 4区 生物学 Q4 GENETICS & HEREDITY Genetics research Pub Date : 2024-02-15 DOI:10.1155/2024/3391054
Z. Firoozi, Elham Mohammadisoleimani, Farzaneh Bagheri, Atefeh Taheri, Babak Pezeshki, M. Naghizadeh, A. Daraei, Jalal Karimi, Yousef Gholampour, Y. Mansoori, Zahra Montaseri
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Abstract

Background and Aims. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a worldwide pandemic, activates signaling cascades and leads to innate immune responses and secretion of multiple chemokines and cytokines. Long noncoding RNAs (lncRNAs) have a crucial role in inflammatory pathways. Through our search on the PubMed database, we discovered that existing research has primarily focused on examining the regulatory impacts of five lncRNAs in the context of viral infections. However, their role in regulating other conditions, including SARS-CoV-2, has not been explored. Therefore, this study aimed to investigate the expression pattern of lncRNAs in the peripheral blood mononuclear cells (PBMC) and their potential roles in SARS-CoV-2 infection. Potentially significant competing endogenous RNA (ceRNA) networks of these five lncRNAs were found using online in-silico techniques. Methods. Ethylenediaminetetraacetic acid (EDTA) blood samples of the control group consisted of 45 healthy people, and a total of 53 COVID-19-infected patients in case group, with a written informed consent, was collected. PBMCs were extracted, and then, the RNA extraction and complementary DNA (cDNA) synthesis was performed. The expression of five lncRNAs (lnc ISR, lnc ATV, lnc PAAN, lnc SG20, and lnc HEAL) was assessed by real-time PCR. In order to evaluate the biomarker roles of genes, receiver operating characteristic (ROC) curve was drawn. Results. Twenty-four (53.3%) and 29 (54.7%) of healthy and COVID-19-infected participants were male, respectively. The most prevalent symptoms were as follows: cough, general weakness, contusion, headache, and sore throat. The results showed that three lncRNAs, including lnc ISR, lnc ATV, and lnc HEAL, were expressed dramatically higher in the case group compared to healthy controls. According to ROC curve analysis, lnc ATV has a higher AUC and is a better biomarker to differentiate COVID-19 patients from the healthy controls. Then, using bioinformatics methods, the ceRNA network of these lncRNAs enabled the identification of mRNAs and miRNAs with crucial functions in COVID-19. Conclusion. The considerable higher expression of ISR, ATV, and HEAL lncRNAs and the significant area under curve (AUC) in ROC curve demonstrate that these RNAs probably have a potential role in controlling the host innate immune responses and regulate the viral replication of SARS-CoV-2. However, these assumptions need further in vitro and in vivo investigations to be confirmed.
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评估 COVID-19 患者感染相关长非编码 RNA 的表达:病例对照研究
背景和目的。严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)是一种全球性流行病,它激活信号级联,导致先天性免疫反应以及多种趋化因子和细胞因子的分泌。长非编码 RNA(lncRNA)在炎症通路中起着至关重要的作用。通过在 PubMed 数据库中搜索,我们发现现有的研究主要集中在研究五种 lncRNA 在病毒感染中的调控作用。然而,它们在调控其他病症(包括 SARS-CoV-2)中的作用尚未得到探讨。因此,本研究旨在调查外周血单核细胞(PBMC)中 lncRNAs 的表达模式及其在 SARS-CoV-2 感染中的潜在作用。本研究利用在线内科学技术发现了这五个lncRNAs潜在的重要竞争性内源性RNA(ceRNA)网络。方法采集45名健康人组成的对照组和53名COVID-19感染者组成的病例组的乙二胺四乙酸(EDTA)血样,并获得知情同意书。提取PBMC后,进行RNA提取和互补DNA(cDNA)合成。实时 PCR 评估了五个 lncRNA(lnc ISR、lnc ATV、lnc PAAN、lnc SG20 和 lnc HEAL)的表达。为了评估基因的生物标记作用,绘制了接收者操作特征曲线(ROC)。结果显示健康和COVID-19感染者中分别有24名(53.3%)和29名(54.7%)男性。最常见的症状如下:咳嗽、全身无力、挫伤、头痛和咽喉痛。结果显示,与健康对照组相比,病例组的三个lncRNA(包括lnc ISR、lnc ATV和lnc HEAL)的表达量显著升高。根据ROC曲线分析,lnc ATV的AUC更高,是区分COVID-19患者和健康对照组的更好的生物标志物。然后,利用生物信息学方法,通过这些 lncRNA 的 ceRNA 网络,确定了在 COVID-19 中具有关键功能的 mRNA 和 miRNA。结论ISR、ATV和HEAL lncRNA的高表达量以及ROC曲线上显著的曲线下面积(AUC)表明,这些RNA可能在控制宿主先天性免疫反应和调节SARS-CoV-2病毒复制中发挥潜在作用。然而,这些假设还需要进一步的体外和体内研究来证实。
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来源期刊
Genetics research
Genetics research 生物-遗传学
自引率
6.70%
发文量
74
审稿时长
>12 weeks
期刊介绍: Genetics Research is a key forum for original research on all aspects of human and animal genetics, reporting key findings on genomes, genes, mutations and molecular interactions, extending out to developmental, evolutionary, and population genetics as well as ethical, legal and social aspects. Our aim is to lead to a better understanding of genetic processes in health and disease. The journal focuses on the use of new technologies, such as next generation sequencing together with bioinformatics analysis, to produce increasingly detailed views of how genes function in tissues and how these genes perform, individually or collectively, in normal development and disease aetiology. The journal publishes original work, review articles, short papers, computational studies, and novel methods and techniques in research covering humans and well-established genetic organisms. Key subject areas include medical genetics, genomics, human evolutionary and population genetics, bioinformatics, genetics of complex traits, molecular and developmental genetics, Evo-Devo, quantitative and statistical genetics, behavioural genetics and environmental genetics. The breadth and quality of research make the journal an invaluable resource for medical geneticists, molecular biologists, bioinformaticians and researchers involved in genetic basis of diseases, evolutionary and developmental studies.
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