Integrated analysis of lncRNA-miRNA-mRNA ceRNA network in neurodegenerative diseases

Mehran Asadi Peighan , Negar Sadat Soleimani Zakeri , Seyed Mehdi Jazayeri , Sajjad Nematzadeh , Habib MotieGhader
{"title":"Integrated analysis of lncRNA-miRNA-mRNA ceRNA network in neurodegenerative diseases","authors":"Mehran Asadi Peighan ,&nbsp;Negar Sadat Soleimani Zakeri ,&nbsp;Seyed Mehdi Jazayeri ,&nbsp;Sajjad Nematzadeh ,&nbsp;Habib MotieGhader","doi":"10.1016/j.neuri.2024.100176","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Neurodegenerative diseases are one of the main causes of physical or behavioral complications which is considered as one of the main health concerns of the elderly population. However, treatment options for neurological diseases are still limited. Recent advances in bioinformatics studies provide an opportunity to understand the mechanisms of these diseases to identify therapeutic targets. In this research, the mRNAs involved in Alzheimer's, Multiple sclerosis, Parkinson's, and Huntington's neurological diseases, which are regulated by upstream factors, have been investigated. Only 2% of all transcripts of a gene are translated into protein and the rest are converted into miRNAs, lncRNAs or circRNAs. miRNAs have crucial role in regulating mRNAs and in a similar sequence lncRNAs or circRNAs are crucial in regulating miRNAs, which disrupts gene expression.</div></div><div><h3>Results</h3><div>To discover above relations in neurodegenerative disease, miRNA-mRNA and lncRNA-miRNA bipartite networks were constructed and then were integrated to construct lncRNA-miRNA-mRNA tripartite networks. Constructing these networks leads to understand deeply about the structure of this mechanism and introducing new biomarkers for the studied diseases. In the next step, enrichment analysis was performed to recognize the genes involved in crucial pathways. Finally, the obtained biomarkers were investigated over the previous studies to prove the accuracy of proposed method.</div></div><div><h3>Conclusions</h3><div>In conclusion, for all four diseases, several numbers of mRNAs, miRNAs and lncRNAs were identified, which are introduced as biomarkers extracted by this study.</div></div>","PeriodicalId":74295,"journal":{"name":"Neuroscience informatics","volume":"4 4","pages":"Article 100176"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroscience informatics","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772528624000219","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Neurodegenerative diseases are one of the main causes of physical or behavioral complications which is considered as one of the main health concerns of the elderly population. However, treatment options for neurological diseases are still limited. Recent advances in bioinformatics studies provide an opportunity to understand the mechanisms of these diseases to identify therapeutic targets. In this research, the mRNAs involved in Alzheimer's, Multiple sclerosis, Parkinson's, and Huntington's neurological diseases, which are regulated by upstream factors, have been investigated. Only 2% of all transcripts of a gene are translated into protein and the rest are converted into miRNAs, lncRNAs or circRNAs. miRNAs have crucial role in regulating mRNAs and in a similar sequence lncRNAs or circRNAs are crucial in regulating miRNAs, which disrupts gene expression.

Results

To discover above relations in neurodegenerative disease, miRNA-mRNA and lncRNA-miRNA bipartite networks were constructed and then were integrated to construct lncRNA-miRNA-mRNA tripartite networks. Constructing these networks leads to understand deeply about the structure of this mechanism and introducing new biomarkers for the studied diseases. In the next step, enrichment analysis was performed to recognize the genes involved in crucial pathways. Finally, the obtained biomarkers were investigated over the previous studies to prove the accuracy of proposed method.

Conclusions

In conclusion, for all four diseases, several numbers of mRNAs, miRNAs and lncRNAs were identified, which are introduced as biomarkers extracted by this study.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
综合分析神经退行性疾病中的 lncRNA-miRNA-mRNA ceRNA 网络
背景神经退行性疾病是导致身体或行为并发症的主要原因之一,被认为是老年人群的主要健康问题之一。然而,神经系统疾病的治疗方案仍然有限。生物信息学研究的最新进展为了解这些疾病的发病机制、确定治疗目标提供了机会。在这项研究中,研究人员调查了阿尔茨海默氏症、多发性硬化症、帕金森氏症和亨廷顿氏症等神经系统疾病中受上游因子调控的 mRNA。一个基因的所有转录本中只有 2% 被翻译成蛋白质,其余的被转化为 miRNA、lncRNA 或 circRNA。miRNA 在调控 mRNA 方面起着关键作用,而与此类似,lncRNA 或 circRNA 在调控 miRNA 方面也起着关键作用,从而干扰基因表达。结果 为了发现神经退行性疾病中的上述关系,研究人员构建了 miRNA-mRNA 和 lncRNA-miRNA 两方网络,然后整合构建了 lncRNA-miRNA-mRNA 三方网络。构建这些网络有助于深入了解这一机制的结构,并为所研究的疾病引入新的生物标记物。下一步是进行富集分析,以识别参与关键通路的基因。最后,对所获得的生物标记物与之前的研究进行了对比,以证明所提方法的准确性。结论总之,本研究针对所有四种疾病鉴定了大量 mRNA、miRNA 和 lncRNA,并将其作为生物标记物进行了提取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Neuroscience informatics
Neuroscience informatics Surgery, Radiology and Imaging, Information Systems, Neurology, Artificial Intelligence, Computer Science Applications, Signal Processing, Critical Care and Intensive Care Medicine, Health Informatics, Clinical Neurology, Pathology and Medical Technology
自引率
0.00%
发文量
0
审稿时长
57 days
期刊最新文献
Integrated analysis of lncRNA-miRNA-mRNA ceRNA network in neurodegenerative diseases Topic modeling of neuropsychiatric diseases related to gut microbiota and gut brain axis using artificial intelligence based BERTopic model on PubMed abstracts Brain network analysis in Parkinson's disease patients based on graph theory Exploring age-related functional brain changes during audio-visual integration tasks in early to mid-adulthood Editorial Board
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1