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MPHGCL-DDI: Meta-Path-Based Heterogeneous Graph Contrastive Learning for Drug-Drug Interaction Prediction.
Hu, Baofang; Yu, Zhenmei; Li, Mingke.
Afiliação
  • Hu B; School of Data and Computer Science, Shandong Women's University, Jinan 250030, China.
  • Yu Z; School of Data and Computer Science, Shandong Women's University, Jinan 250030, China.
  • Li M; School of Information Science and Engineering, University of Jinan, Jinan 250024, China.
Molecules ; 29(11)2024 May 24.
Article em En | MEDLINE | ID: mdl-38893359
ABSTRACT
The combinatorial therapy with multiple drugs may lead to unexpected drug-drug interactions (DDIs) and result in adverse reactions to patients. Predicting DDI events can mitigate the potential risks of combinatorial therapy and enhance drug safety. In recent years, deep models based on heterogeneous graph representation learning have attracted widespread interest in DDI event prediction and have yielded satisfactory results, but there is still room for improvement in prediction performance. In this study, we proposed a meta-path-based heterogeneous graph contrastive learning model, MPHGCL-DDI, for DDI event prediction. The model constructs two contrastive views based on meta-paths an average graph view and an augmented graph view. The former represents that there are connections between drugs, while the latter reveals how the drugs connect with each other. We defined three levels of data augmentation schemes in the augmented graph view and adopted a combination of three losses in the model training phase multi-relation prediction loss, unsupervised contrastive loss and supervised contrastive loss. Furthermore, the model incorporates indirect drug information, protein-protein interactions (PPIs), to reveal latent relations of drugs. We evaluated MPHGCL-DDI on three different tasks of two datasets. Experimental results demonstrate that MPHGCL-DDI surpasses several state-of-the-art methods in performance.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interações Medicamentosas Limite: Humans Idioma: En Revista: Molecules Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interações Medicamentosas Limite: Humans Idioma: En Revista: Molecules Ano de publicação: 2024 Tipo de documento: Article