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Conserved Disease Modules Extracted From Multilayer Heterogeneous Disease and Gene Networks for Understanding Disease Mechanisms and Predicting Disease Treatments

机译:从多层异质性疾病和基因网络中提取的保守性疾病模块以了解疾病的机制并预测疾病的治疗

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摘要

Disease relationship studies for understanding the pathogenesis of complex diseases, diagnosis, prognosis, and drug development are important. Traditional approaches consider one type of disease data or aggregating multiple types of disease data into a single network, which results in important temporal- or context-related information loss and may distort the actual organization. Therefore, it is necessary to apply multilayer network model to consider multiple types of relationships between diseases and the important interplays between different relationships. Further, modules extracted from multilayer networks are smaller and have more overlap that better capture the actual organization. Here, we constructed a weighted four-layer disease-disease similarity network to characterize the associations at different levels between diseases. Then, a tensor-based computational framework was used to extract Conserved Disease Modules (CDMs) from the four-layer disease network. After filtering, nine significant CDMs were reserved. The statistical significance test proved the significance of the nine CDMs. Comparing with modules got from four single layer networks, CMDs are smaller, better represent the actual relationships, and contain potential disease-disease relationships. KEGG pathways enrichment analysis and literature mining further contributed to confirm that these CDMs are highly reliable. Furthermore, the CDMs can be applied to predict potential drugs for diseases. The molecular docking techniques were used to provide the direct evidence for drugs to treat related disease. Taking Rheumatoid Arthritis (RA) as a case, we found its three potential drugs Carvedilol, Metoprolol, and Ramipril. And many studies have pointed out that Carvedilol and Ramipril have an effect on RA. Overall, the CMDs extracted from multilayer networks provide us with an impressive understanding disease mechanisms from the perspective of multi-layer network and also provide an effective way to predict potential drugs for diseases based on its neighbors in a same CDM.
机译:疾病关系研究对于理解复杂疾病的发病机理,诊断,预后和药物开发非常重要。传统方法考虑一种类型的疾病数据或将多种类型的疾病数据汇总到单个网络中,这会导致与时间或上下文相关的重要信息丢失,并可能扭曲实际组织。因此,有必要应用多层网络模型来考虑疾病之间多种类型的关系以及不同关系之间的重要相互作用。此外,从多层网络中提取的模块较小,并且具有更多的重叠,可以更好地捕获实际组织。在这里,我们构建了一个加权的四层疾病-疾病相似性网络来表征疾病之间不同级别的关联。然后,使用基于张量的计算框架从四层疾病网络中提取保守疾病模块(CDM)。过滤后,保留了九个重要的CDM。统计显着性检验证明了这9个CDM的显着性。与从四个单层网络获得的模块相比,CMD较小,可以更好地表示实际关系,并且包含潜在的疾病-疾病关系。 KEGG途径富集分析和文献挖掘进一步有助于证实这些CDM高度可靠。此外,CDM可以用于预测潜在的疾病药物。分子对接技术被用来为药物治疗相关疾病提供直接证据。以类风湿关节炎(RA)为例,我们发现了它的三种潜在药物卡维地洛,美托洛尔和雷米普利。许多研究指出,卡维地洛和雷米普利对类风湿关节炎有影响。总体而言,从多层网络中提取的CMD从多层网络的角度为我们提供了令人印象深刻的疾病机制,也为基于同一CDM中的邻居预测潜在的疾病药物提供了有效的方法。

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