DSE-HNGCN:基于挖掘药物和副作用相互作用的异构网络预测药物副作用频率。

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2024-12-16 DOI:10.1016/j.jmb.2024.168916
Xuhao Ma, Tingfang Wu, Geng Li, Junkai Wang, Yelu Jiang, Lijun Quan, Qiang Lyu
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引用次数: 0

摘要

评估药物副作用的频率在药物开发和风险-效益分析中至关重要。虽然现有的深度学习方法显示出希望,但它们尚未探索使用异构网络同时模拟药物和副作用之间的各种关系,突出潜在增强的领域。在这项研究中,我们提出了DSE-HNGCN,这是一种利用异构网络同时模拟药物和副作用之间各种关系的新方法。通过使用多层图卷积网络,我们的目标是挖掘药物和副作用之间的相互作用,以预测药物副作用的频率。为了解决图卷积网络中的过度平滑问题,并从不同的层捕获不同的语义信息,我们引入了一种层重要性组合策略。此外,我们还开发了一个集成的预测模块,有效地利用了来自不同网络的药物和副作用特征。我们在一系列场景中使用基准数据集的实验结果表明,我们的模型在预测药物副作用频率方面优于现有方法。对比实验和可视化分析强调了整合异构网络和其他相关模块的实质性好处,从而提高了DSE-HNGCN预测的准确性。我们还为DSE-HNGCN提供了可解释性,表明提取的特征具有潜在的生物学意义。案例研究验证了我们的模型识别药物潜在副作用的能力,为后续的生物验证实验提供了有价值的见解。
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DSE-HNGCN: Predicting the frequencies of drug-side effects based on heterogeneous networks with mining interactions between drugs and side effects.

Evaluating the frequencies of drug-side effects is crucial in drug development and risk-benefit analysis. While existing deep learning methods show promise, they have yet to explore using heterogeneous networks to simultaneously model the various relationship between drugs and side effects, highlighting areas for potential enhancement. In this study, we propose DSE-HNGCN, a novel method that leverages heterogeneous networks to simultaneously model the various relationships between drugs and side effects. By employing multi-layer graph convolutional networks, we aim to mine the interactions between drugs and side effects to predict the frequencies of drug-side effects. To address the over-smoothing problem in graph convolutional networks and capture diverse semantic information from different layers, we introduce a layer importance combination strategy. Additionally, we have developed an integrated prediction module that effectively utilizes drug and side effect features from different networks. Our experimental results, using benchmark datasets in a range of scenarios, show that our model outperforms existing methods in predicting the frequencies of drug-side effects. Comparative experiments and visual analysis highlight the substantial benefits of incorporating heterogeneous networks and other pertinent modules, thus improving the accuracy of DSE-HNGCN predictions. We also provide interpretability for DSE-HNGCN, indicating that the extracted features are potentially biologically significant. Case studies validate our model's capability to identify potential side effects of drugs, offering valuable insights for subsequent biological validation experiments.

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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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