摘要
背景:阿尔茨海默病(AD)仍然是人类健康的主要威胁之一。尽管尚未发现令人满意的 AD 治疗方法,但仍有必要继续寻找新的方法来应对这种隐匿且使人衰弱的疾病。尽管大量研究表明长链非编码 RNA (lncRNA) 在多种疾病中发挥重要作用,但它们在 AD 中的作用仍不清楚。 目的:通过数据分析探讨lncRNA在AD病程中的作用,加深我们对AD的认识,期待为AD的治疗找到新的突破口。 方法:我们从Gene Expression Omnibus数据库中下载并筛选AD患者海马区的表达数据。我们基于竞争性内源性 RNA (ceRNA) 假设生成 lncRNA-miRNA-mRNA 网络,并根据基因表达水平构建编码-非编码共表达 (CNC) 网络,然后执行顺式和反式调节分析。 结果:通过综合系统分析,我们发现lncRNAs MALAT1、OIP5-AS1、LINC00657和lnc-NUMB-1调控AD关键致病基因APP、PSEN1、BACE1的表达;并且这些lncRNA可能通过外泌体促进β-淀粉样蛋白(Aβ蛋白)在大脑中的分布。此外,发现 lncRNA 可以调节病毒转录表达,从而进一步支持 AD 的病毒发病机制。 结论:存在于AD患者海马区的lncRNAs MALAT1、OIP5-AS1、LINC00657和lnc-NUMB-1对该病的发生发展具有重要影响。
关键词: AD、CNC 网络、顺式和反式调节、TF、ceRNA、lncRNA。
Current Alzheimer Research
Title:Comprehensive Analysis of Differential Expression Profiles of Long Noncoding RNAs with Associated Co-expression and Competing Endogenous RNA Networks in the Hippocampus of Patients with Alzheimer's Disease
Volume: 18 Issue: 11
关键词: AD、CNC 网络、顺式和反式调节、TF、ceRNA、lncRNA。
摘要:
Background: Alzheimer's disease (AD) is still one of the major threats to human health. Although a satisfactory treatment for AD has not yet been discovered, it is necessary to continue to search for novel approaches to deal with this insidious and debilitating disease. Although numerous studies have shown that long non-coding RNA (lncRNA) occupy a significant role in a variety of diseases, their roles in AD remain unclear.
Objective: Using data analysis to explore the role of lncRNA in the course of AD, to further our understanding of AD, and to look forward to finding a new breakthrough for the treatment of AD.
Methods: We downloaded and screened expression data of the hippocampal regions of patients with AD from the Gene Expression Omnibus database. We generated lncRNA-miRNA-mRNA networks based on the competing endogenous RNA (ceRNA) hypothesis, and according to gene expression level, we constructed a coding-noncoding co-expression (CNC) network and then executed cis- and trans-regulation analyses.
Results: Through comprehensive and systematic analyses, we found that lncRNAs MALAT1, OIP5-AS1, LINC00657, and lnc-NUMB-1 regulated the expression of the key AD pathogenic genes APP, PSEN1, BACE1; and that these lncRNAs may promote the distribution of β-amyloid (Aβ protein) in the brain through exosomes. In addition, lncRNAs were found to adjust viral transcriptional expression, thereby further supporting viral pathogenesis for AD.
Conclusion: The lncRNAs MALAT1, OIP5-AS1, LINC00657, and lnc-NUMB-1 that are present in the hippocampus of AD patients exert an important influence on the development of this disease.
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Cite this article as:
Comprehensive Analysis of Differential Expression Profiles of Long Noncoding RNAs with Associated Co-expression and Competing Endogenous RNA Networks in the Hippocampus of Patients with Alzheimer's Disease, Current Alzheimer Research 2021; 18 (11) . https://dx.doi.org/10.2174/1567205018666211202143449
DOI https://dx.doi.org/10.2174/1567205018666211202143449 |
Print ISSN 1567-2050 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5828 |
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