School of Computer Science and Technology, Heilongjiang University, Harbin 150080, China.
School of Mathematical Science, Heilongjiang University, Harbin 150080, China.
Cells. 2019 Jul 11;8(7):705. doi: 10.3390/cells8070705.
Identifying novel indications for approved drugs can accelerate drug development and reduce research costs. Most previous studies used shallow models for prioritizing the potential drug-related diseases and failed to deeply integrate the paths between drugs and diseases which may contain additional association information. A deep-learning-based method for predicting drug-disease associations by integrating useful information is needed. We proposed a novel method based on a convolutional neural network (CNN) and bidirectional long short-term memory (BiLSTM)-CBPred-for predicting drug-related diseases. Our method deeply integrates similarities and associations between drugs and diseases, and paths among drug-disease pairs. The CNN-based framework focuses on learning the original representation of a drug-disease pair from their similarities and associations. As the drug-disease association possibility also depends on the multiple paths between them, the BiLSTM-based framework mainly learns the path representation of the drug-disease pair. In addition, considering that different paths have discriminate contributions to the association prediction, an attention mechanism at path level is constructed. Our method, CBPred, showed better performance and retrieved more real associations in the front of the results, which is more important for biologists. Case studies further confirmed that CBPred can discover potential drug-disease associations.
确定已批准药物的新适应症可以加速药物开发并降低研究成本。以前的大多数研究都使用浅层模型来确定潜在的药物相关疾病的优先级,而未能深入整合药物与疾病之间的途径,这些途径可能包含其他关联信息。需要一种基于深度学习的方法来通过整合有用信息来预测药物-疾病关联。我们提出了一种基于卷积神经网络 (CNN) 和双向长短期记忆 (BiLSTM) 的新方法 CBPred,用于预测药物相关疾病。我们的方法深入整合了药物和疾病之间的相似性和关联,以及药物-疾病对之间的路径。基于 CNN 的框架专注于从相似性和关联中学习药物-疾病对的原始表示。由于药物-疾病关联的可能性也取决于它们之间的多条路径,因此基于 BiLSTM 的框架主要学习药物-疾病对的路径表示。此外,考虑到不同的路径对关联预测有区分贡献,构建了路径级别的注意力机制。我们的方法 CBPred 在结果的前面显示出更好的性能并检索到更多真实的关联,这对生物学家来说更为重要。案例研究进一步证实,CBPred 可以发现潜在的药物-疾病关联。