Yu Liang, Yao Shunyu, Gao Lin, Zha Yunhong
School of Computer Science and Technology, Xidian University, Xi'an, China.
Department of Neurology, Institute of Neural Regeneration and Repair, Three Gorges University College of Medicine, The First Hospital of Yichang, Yichang, China.
Front Genet. 2019 Jan 18;9:745. doi: 10.3389/fgene.2018.00745. eCollection 2018.
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.
疾病关系研究对于理解复杂疾病的发病机制、诊断、预后及药物研发具有重要意义。传统方法只考虑一种疾病数据或将多种疾病数据聚合到单个网络中,这会导致重要的时间或上下文相关信息丢失,并可能扭曲实际结构。因此,有必要应用多层网络模型来考虑疾病之间的多种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更小且重叠更多,能更好地捕捉实际结构。在此,我们构建了一个加权四层疾病-疾病相似性网络,以表征疾病之间不同层次的关联。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)。经过筛选,保留了9个显著的CDM。统计显著性检验证明了这9个CDM的显著性。与从四个单层网络得到的模块相比,CMD更小,能更好地代表实际关系,并包含潜在的疾病-疾病关系。KEGG通路富集分析和文献挖掘进一步证实这些CDM高度可靠。此外,CDM可用于预测疾病的潜在药物。分子对接技术为治疗相关疾病的药物提供了直接证据。以类风湿性关节炎(RA)为例,我们发现了其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RA有作用。总体而言,从多层网络中提取的CMD从多层网络角度为我们理解疾病机制提供了深刻见解,也为基于同一CDM中的邻居预测疾病潜在药物提供了有效方法。