Revealing the Modular Similarities and Differences Among Alzheimer's Disease, Vascular Dementia, and Parkinson's Disease in Genomic Networks.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2022-06-01 Epub Date: 2021-06-12 DOI:10.1007/s12017-021-08670-2
Yafei Chen, Qiong Liu, Jun Liu, Penglu Wei, Bing Li, Nongyun Wang, Zhenquan Liu, Zhong Wang
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引用次数: 7

Abstract

Alzheimer's disease (AD), vascular dementia (VD), and Parkinson's disease (PD) exert increasingly lethal or disabling effects on humans, but the associations among these diseases at the molecular level remain unclear. In our research, lists of genes related to these three diseases were acquired from public databases. We constructed gene-gene networks of the lists of disease-related genes using the STRING database and selected the plug-in MCODE as the most suitable method to divide the three disease-associated networks into modules through an entropy calculation. Notably, 1173 AD-related, 203 VD-related, and 722 PD-related genes as well as 72 overlapping genes were observed among the three diseases. By dividing the modules from the gene network, we divided the AD-related gene network into 27 modules, the VD-related gene network into 8 modules, and the PD-related gene network into 17 modules. After the enrichment analysis of each disease-related gene, 146 overlapping biological processes and 32 overlapping pathways were identified. Ultimately, through similarity analysis of the genes, biological processes, and pathways, we found that AD and VD were the most closely related at the biological process and pathway levels, with similarity coefficients of 0.2784 and 0.3626, respectively. After analyzing the overlapping gene network, we found that INS might play an important role in the network and that insulin and its signaling pathways may play a key role in these neurodegenerative diseases. Our research illustrates a new method for in-depth research on the three diseases, which may accelerate the progress of developing new therapeutics and may be applied to prevent neurodegenerative diseases.

揭示基因组网络中阿尔茨海默病、血管性痴呆和帕金森病的模块异同。
阿尔茨海默病(AD)、血管性痴呆(VD)和帕金森病(PD)对人类的致命或致残作用越来越大,但这些疾病在分子水平上的关联尚不清楚。在我们的研究中,我们从公共数据库中获得了与这三种疾病相关的基因列表。我们使用STRING数据库构建疾病相关基因列表的基因-基因网络,并选择插件MCODE作为最合适的方法,通过熵计算将三个疾病相关网络划分为模块。值得注意的是,三种疾病中分别有1173个ad相关基因、203个vd相关基因、722个pd相关基因和72个重叠基因。通过对基因网络进行模块划分,我们将ad相关基因网络划分为27个模块,将dvd相关基因网络划分为8个模块,将pd相关基因网络划分为17个模块。通过对每个疾病相关基因的富集分析,鉴定出146个重叠的生物学过程和32个重叠的通路。最终,通过对基因、生物过程和途径的相似性分析,我们发现AD和VD在生物过程和途径水平上关系最为密切,相似系数分别为0.2784和0.3626。通过对重叠基因网络的分析,我们发现INS可能在网络中起重要作用,胰岛素及其信号通路可能在这些神经退行性疾病中起关键作用。我们的研究为深入研究这三种疾病提供了一种新的方法,这可能会加速开发新的治疗方法的进展,并可能应用于预防神经退行性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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