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首页> 外文期刊>BMC Systems Biology >Predicting and understanding comprehensive drug-drug interactions via semi-nonnegative matrix factorization
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Predicting and understanding comprehensive drug-drug interactions via semi-nonnegative matrix factorization

机译:通过半负矩阵分解预测和理解全面的药物相互作用

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Drug-drug interactions (DDIs) always cause unexpected and even adverse drug reactions. It is important to identify DDIs before drugs are used in the market. However, preclinical identification of DDIs requires much money and time. Computational approaches have exhibited their abilities to predict potential DDIs on a large scale by utilizing pre-market drug properties (e.g. chemical structure). Nevertheless, none of them can predict two comprehensive types of DDIs, including enhancive and degressive DDIs, which increases and decreases the behaviors of the interacting drugs respectively. There is a lack of systematic analysis on the structural relationship among known DDIs. Revealing such a relationship is very important, because it is able to help understand how DDIs occur. Both the prediction of comprehensive DDIs and the discovery of structural relationship among them play an important guidance when making a co-prescription. In this work, treating a set of comprehensive DDIs as a signed network, we design a novel model (DDINMF) for the prediction of enhancive and degressive DDIs based on semi-nonnegative matrix factorization. Inspiringly, DDINMF achieves the conventional DDI prediction (AUROC?=?0.872 and AUPR?=?0.605) and the comprehensive DDI prediction (AUROC?=?0.796 and AUPR?=?0.579). Compared with two state-of-the-art approaches, DDINMF shows it superiority. Finally, representing DDIs as a binary network and a signed network respectively, an analysis based on NMF reveals crucial knowledge hidden among DDIs. Our approach is able to predict not only conventional binary DDIs but also comprehensive DDIs. More importantly, it reveals several key points about the?DDI network: (1) both binary and signed networks show fairly clear clusters, in which both?drug degree and the difference between positive degree and negative degree show significant distribution; (2) the drugs having large degrees tend to have a larger difference between positive degree and negative degree; (3) though the binary DDI network contains no information about enhancive and degressive DDIs at all, it implies some of their relationship in the comprehensive DDI matrix; (4) the occurrence of signs indicating enhancive and degressive DDIs is not random because the comprehensive DDI network is equipped with a structural balance.
机译:药物相互作用(DDI)总是会引起意料之外的甚至不利的药物反应。在市场上使用毒品之前,必须先确定DDI。但是,DDI的临床前鉴定需要大量金钱和时间。计算方法已经显示出了通过利用上市前药物特性(例如化学结构)来大规模预测潜在DDI的能力。然而,它们都无法预测两种综合类型的DDI,包括增强型DDI和递减型DDI,它们分别增加和减少了相互作用药物的行为。缺乏对已知DDI之间的结构关系的系统分析。揭示这种关系非常重要,因为它可以帮助理解DDI的发生方式。在制定共同处方时,对综合DDI的预测和发现它们之间的结构关系都起着重要的指导作用。在这项工作中,将一组全面的DDI视为一个带符号的网络,我们设计了一种基于半负矩阵分解的增强和退化DDI预测的新模型(DDINMF)。令人鼓舞地,DDINMF实现了常规的DDI预测(AUROCα= 0.872和AUPRα= 0.605)和综合的DDI预测(AUROCα= 0.796和AUPRα= 0.579)。与两种最先进的方法相比,DDINMF显示出它的优越性。最后,将DDI分别表示为二进制网络和有符号网络,基于NMF的分析揭示了DDI中隐藏的关键知识。我们的方法不仅能够预测常规二进制DDI,而且能够预测全面的DDI。更重要的是,它揭示了有关DDI网络的几个关键点:(1)二元网络和有符号网络都显示出相当清晰的簇,其中药物度以及正度和负度之间的差异都显示出显着的分布; (2)度数大的药物在正度和负度之间往往相差较大; (3)尽管二进制DDI网络根本不包含任何有关增强和退化DDI的信息,但它暗示了它们在综合DDI矩阵中的某些关系; (4)指示DDI增强和下降的迹象的出现不是随机的,因为全面的DDI网络具有结构上的平衡。

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