ArticleMolecules (Basel, Switzerland)2019
Drug Side-Effect Prediction Via Random Walk on the Signed Heterogeneous Drug Network.
Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed.
- MGPT: A Multi-task Graph Prompt Learning Framework for Drug Discovery.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Graph reasoning method enhanced by relational transformers and knowledge distillation for drug-related side effect prediction.iScience · 2024Article
- HMMF: a hybrid multi-modal fusion framework for predicting drug side effect frequencies.BMC bioinformatics · 2024Article
- Learning Multi-Types of Neighbor Node Attributes and Semantics by Heterogeneous Graph Transformer and Multi-View Attention for Drug-Related Side-Effect Prediction.Molecules (Basel, Switzerland) · 2023Article
- Interpretable Drug-to-Drug Network Features for Predicting Adverse Drug Reactions.Healthcare (Basel, Switzerland) · 2023Article
- Graph generative and adversarial strategy-enhanced node feature learning and self-calibrated pairwise attribute encoding for prediction of drug-related side effects.Frontiers in pharmacology · 2023Article
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Authors and funding
3 authors.
Funding
Abstract
Drug side-effects have become a major public health concern as they are the underlying cause of over a million serious injuries and deaths each year. Therefore, it is of critical importance to detect side-effects as early as possible. Existing computational methods mainly utilize the drug chemical profile and the drug biological profile to predict the side-effects of a drug. In the utilized drug biological profile information, they only focus on drug-target interactions and neglect the modes of action of drugs on target proteins. In this paper, we develop a new method for predicting potential side-effects of drugs based on more comprehensive drug information in which the modes of action of drugs on target proteins are integrated. Drug information of multiple types is modeled as a signed heterogeneous information network. We propose a signed heterogeneous information network embedding framework for learning drug embeddings and predicting side-effects of drugs. We use two bias random walk procedures to obtain drug sequences and train a Skip-gram model to learn drug embeddings. We experimentally demonstrate the performance of the proposed method by comparison with state-of-the-art methods. Furthermore, the results of a case study support our hypothesis that modes of action of drugs on target proteins are meaningful in side-effect prediction.
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