Kim Yoonbee, Cho Young-Rae
Division of Software, Yonsei University Mirae Campus, Wonju-si 26493, Gangwon-do, Republic of Korea.
Division of Digital Healthcare, Yonsei University Mirae Campus, Wonju-si 26493, Gangwon-do, Republic of Korea.
Biomedicines. 2023 Jul 14;11(7):1998. doi: 10.3390/biomedicines11071998.
Drug repositioning offers the significant advantage of greatly reducing the cost and time of drug discovery by identifying new therapeutic indications for existing drugs. In particular, computational approaches using networks in drug repositioning have attracted attention for inferring potential associations between drugs and diseases efficiently based on the network connectivity. In this article, we proposed a network-based drug repositioning method to construct a drug-gene-disease tensor by integrating drug-disease, drug-gene, and disease-gene associations and predict drug-gene-disease triple associations through tensor decomposition. The proposed method, which ensembles generalized tensor decomposition (GTD) and multi-layer perceptron (MLP), models drug-gene-disease associations through GTD and learns the features of drugs, genes, and diseases through MLP, providing more flexibility and non-linearity than conventional tensor decomposition. We experimented with drug-gene-disease association prediction using two distinct networks created by chemical structures and ATC codes as drug features. Moreover, we leveraged drug, gene, and disease latent vectors obtained from the predicted triple associations to predict drug-disease, drug-gene, and disease-gene pairwise associations. Our experimental results revealed that the proposed ensemble method was superior for triple association prediction. The ensemble model achieved an AUC of 0.96 in predicting triple associations for new drugs, resulting in an approximately 7% improvement over the performance of existing models. It also showed competitive accuracy for pairwise association prediction compared with previous methods. This study demonstrated that incorporating genetic information leads to notable advancements in drug repositioning.
药物重新定位具有显著优势,即通过识别现有药物的新治疗适应症,可大幅降低药物研发的成本和时间。特别是,在药物重新定位中使用网络的计算方法,因能基于网络连通性有效推断药物与疾病之间的潜在关联而受到关注。在本文中,我们提出了一种基于网络的药物重新定位方法,通过整合药物 - 疾病、药物 - 基因和疾病 - 基因关联来构建药物 - 基因 - 疾病张量,并通过张量分解预测药物 - 基因 - 疾病三元关联。所提出的方法结合了广义张量分解(GTD)和多层感知器(MLP),通过GTD对药物 - 基因 - 疾病关联进行建模,并通过MLP学习药物、基因和疾病的特征,比传统张量分解提供了更大的灵活性和非线性。我们使用由化学结构和ATC代码作为药物特征创建的两个不同网络,对药物 - 基因 - 疾病关联预测进行了实验。此外,我们利用从预测的三元关联中获得的药物、基因和疾病潜在向量,来预测药物 - 疾病、药物 - 基因和疾病 - 基因的成对关联。我们的实验结果表明,所提出的集成方法在三元关联预测方面表现更优。该集成模型在预测新药的三元关联时,AUC达到了0.96,比现有模型的性能提高了约7%。与先前方法相比,它在成对关联预测方面也显示出具有竞争力的准确性。这项研究表明,纳入遗传信息会在药物重新定位方面带来显著进展。