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Exploration of attractor modules for sporadic amyotrophic lateral sclerosis via systemic module inference and attract method

机译:通过系统模块推断和吸引方法探索散发性肌萎缩性侧索硬化的吸引子模块

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摘要

Sporadic amyotrophic lateral sclerosis (SALS) is a devastating neurodegenerative disorder. However, the understanding of SALS is still poor. This research aimed to excavate attractor modules for SALS by integrating the systemic module inference and attract method. To achieve this, gene expression data and protein-protein data were recruited and preprocessed. Then, based on the Spearman's correlation coefficient (SCC) of the interactions under these two conditions, two PPI networks separately with 870 nodes (979 interactions) in normal control group and 601 nodes (777 interactions) in SALS group were built. Systemic module inference method was performed to identify the modules, and attract method was used to identify attractor modules. Finally, pathway enrichment analysis was performed to disclose the functional enrichment of these attractor modules. In total 44 and 118 modules were identified for normal control and SALS groups, respectively. Among them, 6 modules were with similar gene composition between the two groups, and all 6 modules were considered as the attractor module via attract method. These attractor modules might be potential biomarkers for early diagnosis and therapy of SALS, which could provide insight into the disease biology and suggest possible directions for drug screening programs.
机译:偶发性肌萎缩性侧索硬化症(SALS)是毁灭性的神经退行性疾病。但是,对SALS的理解仍然很差。这项研究旨在通过集成系统模块推断和吸引方法来挖掘SALS吸引子模块。为了达到这个目的,募集并预处理了基因表达数据和蛋白质-蛋白质数据。然后,基于这两个条件下交互作用的斯皮尔曼相关系数(SCC),建立了两个PPI网络,分别具有正常对照组的870个节点(979个交互)和SALS组的601个节点(777个交互)。进行系统的模块推断方法识别模块,并使用吸引方法识别吸引模块。最后,进行路径富集分析以揭示这些吸引子模块的功能富集。分别为正常对照组和SALS组确定了44个模块和118个模块。其中,两组之间具有相似基因组成的6个模块,通过吸引法将6个模块全部视为吸引子模块。这些吸引子模块可能是SALS早期诊断和治疗的潜在生物标志物,可以提供对疾病生物学的深入了解并为药物筛选计划提供可能的方向。

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