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元数据分析以探索影响SARS-CoV-2感染的枢纽基因的核心,突出其发病机制和药物再利用。

Meta-Data Analysis to Explore the Hub of the Hub-Genes That Influence SARS-CoV-2 Infections Highlighting Their Pathogenetic Processes and Drugs Repurposing.

作者信息

Mosharaf Md Parvez, Kibria Md Kaderi, Hossen Md Bayazid, Islam Md Ariful, Reza Md Selim, Mahumud Rashidul Alam, Alam Khorshed, Gow Jeff, Mollah Md Nurul Haque

机构信息

Bioinformatics Lab, Department of Statistics, University of Rajshahi, Rajshahi 6205, Bangladesh.

School of Business, Faculty of Business, Education, Law and Arts, University of Southern Queensland, Toowoomba, QLD 4350, Australia.

出版信息

Vaccines (Basel). 2022 Aug 3;10(8):1248. doi: 10.3390/vaccines10081248.

Abstract

The pandemic of SARS-CoV-2 infections is a severe threat to human life and the world economic condition. Although vaccination has reduced the outspread, but still the situation is not under control because of the instability of RNA sequence patterns of SARS-CoV-2, which requires effective drugs. Several studies have suggested that the SARS-CoV-2 infection causing hub differentially expressed genes (Hub-DEGs). However, we observed that there was not any common hub gene (Hub-DEGs) in our analyses. Therefore, it may be difficult to take a common treatment plan against SARS-CoV-2 infections globally. The goal of this study was to examine if more representative Hub-DEGs from published studies by means of hub of Hub-DEGs (hHub-DEGs) and associated potential candidate drugs. In this study, we reviewed 41 articles on transcriptomic data analysis of SARS-CoV-2 and found 370 unique hub genes or studied genes in total. Then, we selected 14 more representative Hub-DEGs (, , , , , , , , , , , , , ) as hHub-DEGs by their protein-protein interaction analysis. Their associated biological functional processes, transcriptional, and post-transcriptional regulatory factors. Then we detected hHub-DEGs guided top-ranked nine candidate drug agents (Digoxin, Avermectin, Simeprevir, Nelfinavir Mesylate, Proscillaridin, Linifanib, Withaferin, Amuvatinib, Atazanavir) by molecular docking and cross-validation for treatment of SARS-CoV-2 infections. Therefore, the findings of this study could be useful in formulating a common treatment plan against SARS-CoV-2 infections globally.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的大流行对人类生命和世界经济状况构成了严重威胁。尽管疫苗接种减少了病毒传播,但由于SARS-CoV-2 RNA序列模式的不稳定性,情况仍未得到控制,这就需要有效的药物。多项研究表明,SARS-CoV-2感染会导致枢纽差异表达基因(Hub-DEGs)。然而,我们观察到在我们的分析中没有任何共同的枢纽基因(Hub-DEGs)。因此,制定全球统一的针对SARS-CoV-2感染的治疗方案可能会很困难。本研究的目的是通过枢纽差异表达基因的枢纽(hHub-DEGs)及相关潜在候选药物,检验已发表研究中是否存在更具代表性的Hub-DEGs。在本研究中,我们回顾了41篇关于SARS-CoV-2转录组数据分析的文章,共发现370个独特的枢纽基因或研究基因。然后,通过蛋白质-蛋白质相互作用分析,我们选择了14个更具代表性的Hub-DEGs(……)作为hHub-DEGs。分析了它们相关的生物学功能过程、转录和转录后调控因子。然后,我们通过分子对接和交叉验证检测了hHub-DEGs指导的排名前九的候选药物制剂(地高辛、阿维菌素、西米普韦、甲磺酸奈非那韦、海葱苷、林尼法尼、Withaferin、阿穆瓦替尼、阿扎那韦)用于治疗SARS-CoV-2感染。因此,本研究结果可能有助于制定全球统一的针对SARS-CoV-2感染的治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8e6/9415433/5b770109494b/vaccines-10-01248-g001.jpg

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