A model-agnostic framework to enhance knowledge graph-based drug combination prediction with drug-drug interaction data and supervised contrastive learning

被引:4
作者
Gu, Jeonghyeon [1 ]
Bang, Dongmin [2 ]
Yi, Jungseob [1 ]
Lee, Sangseon [3 ]
Kim, Dong Kyu [4 ]
Kim, Sun [5 ]
机构
[1] Seoul Natl Univ, Interdisciplinary Program Artificial Intelligence, Seoul, South Korea
[2] Seoul Natl Univ, Interdisciplinary Program Bioinformat, Seoul, South Korea
[3] Seoul Natl Univ, Inst Comp Technol, Seoul, South Korea
[4] PHARMGENSCIENCE, Drug Discovery R&D Ctr, Hwaseong, South Korea
[5] Seoul Natl Univ SNU, Dept Comp Sci & Engn, Bioinformat & Interdisciplinary Program Artificial, Interdisciplinary Program, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
drug combination; knowledge graph; drug-drug interaction; supervised contrastive learning; random walk; graph neural network; FIXED-DOSE COMBINATION; THERAPY; HYPERTENSION; MANAGEMENT; INHIBITORS; IDENTIFY; EFFICACY; SYNERGY; SAFETY;
D O I
10.1093/bib/bbad285
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Combination therapies have brought significant advancements to the treatment of various diseases in the medical field. However, searching for effective drug combinations remains a major challenge due to the vast number of possible combinations. Biomedical knowledge graph (KG)-based methods have shown potential in predicting effective combinations for wide spectrum of diseases, but the lack of credible negative samples has limited the prediction performance of machine learning models. To address this issue, we propose a novel model-agnostic framework that leverages existing drug-drug interaction (DDI) data as a reliable negative dataset and employs supervised contrastive learning (SCL) to transform drug embedding vectors to be more suitable for drug combination prediction. We conducted extensive experiments using various network embedding algorithms, including random walk and graph neural networks, on a biomedical KG. Our framework significantly improved performance metrics compared to the baseline framework. We also provide embedding space visualizations and case studies that demonstrate the effectiveness of our approach. This work highlights the potential of using DDI data and SCL in finding tighter decision boundaries for predicting effective drug combinations.
引用
收藏
页数:11
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