计算机科学
语义学(计算机科学)
特征(语言学)
机制(生物学)
人工智能
联想(心理学)
节点(物理)
数据挖掘
融合机制
机器学习
传感器融合
构造(python库)
药物重新定位
航程(航空)
特征提取
数据集成
数据驱动
信息融合
药物靶点
作者
Yue Huang,Dandan Li,Weizhong Zhao,Xianjun Shen
出处
期刊:
日期:2025-12-03
卷期号:23 (1): 259-270
标识
DOI:10.1109/tcbbio.2025.3639821
摘要
Drug repositioning is an efficient drug discovery method for identifying associations between present drugs and new diseases, offering considerable development time and cost savings. Although existing methods have been widely applied, they fail to fully capture the complex semantics between drugs and diseases, and are deficient in terms of model interpretability. In this paper, we propose a novel method using a hierarchical attention mechanism aggregating meta-path information for drug-disease association prediction (MPHAM), aiming at effectively integrating heterogeneous information from various sources to enhance prediction accuracy and model interpretability. First, considering the wide range of biological interactions between drugs and diseases, we construct a heterogeneous information network (HIN) to utilize data on drugs, proteins, and diseases. Then, we introduce a meta-path-based feature fusion strategy designed to effectively capture the complex semantics between nodes in the network. By defining meta-paths of multiple lengths and types, information about different relationship types is systematically integrated to generate high-quality node feature representations. Furthermore, the feature fusion strategy incorporates a multi-layer attention mechanism that dynamically assigns weights to the contributions of various meta-paths in the feature aggregation process, significantly improving the model's capacity to capture important semantic information. Experimental results demonstrate that MPHAM can effectively predict drug-disease association by integrating complex meta-path information, and the prediction accuracy is better than five state-of-the-art methods. The case studies of three classical drugs further demonstrate the more accurate predictive performance of MPHAM in drug-candidate disease association prediction.
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