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用于药物重定位的基于梯度平衡的异构图对比学习

Heterogeneous graph contrastive learning with gradient balance for drug repositioning.

作者信息

Cui Hai, Duan Meiyu, Bi Haijia, Li Xiaobo, Hou Xiaodi, Zhang Yijia

机构信息

Information Science and Technology College, Dalian Maritime University, No.1 Linghai Road, Dalian 116026, Liaoning, China.

College of Computer Science and Technology, Jilin University, No.2699 Qianjin Street, Changchun 130012, Jilin, China.

出版信息

Brief Bioinform. 2024 Nov 22;26(1). doi: 10.1093/bib/bbae650.

DOI:10.1093/bib/bbae650
PMID:39692448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11653209/
Abstract

Drug repositioning, which involves identifying new therapeutic indications for approved drugs, is pivotal in accelerating drug discovery. Recently, to mitigate the effect of label sparsity on inferring potential drug-disease associations (DDAs), graph contrastive learning (GCL) has emerged as a promising paradigm to supplement high-quality self-supervised signals through designing auxiliary tasks, then transfer shareable knowledge to main task, i.e. DDA prediction. However, existing approaches still encounter two limitations. The first is how to generate augmented views for fully capturing higher-order interaction semantics. The second is the optimization imbalance issue between auxiliary and main tasks. In this paper, we propose a novel heterogeneous Graph Contrastive learning method with Gradient Balance for DDA prediction, namely GCGB. To handle the first challenge, a fusion view is introduced to integrate both semantic views (drug and disease similarity networks) and interaction view (heterogeneous biomedical network). Next, inter-view contrastive learning auxiliary tasks are designed to contrast the fusion view with semantic and interaction views, respectively. For the second challenge, we adaptively adjust the gradient of GCL auxiliary tasks from the perspective of gradient direction and magnitude for better guiding parameter update toward main task. Extensive experiments conducted on three benchmarks under 10-fold cross-validation demonstrate the model effectiveness.

摘要

药物重新定位,即确定已批准药物的新治疗适应症,在加速药物发现过程中起着关键作用。最近,为了减轻标签稀疏性对推断潜在药物-疾病关联(DDA)的影响,图对比学习(GCL)作为一种有前景的范式出现了,它通过设计辅助任务来补充高质量的自监督信号,然后将可共享的知识转移到主要任务,即DDA预测。然而,现有方法仍然存在两个局限性。第一个是如何生成增强视图以充分捕捉高阶交互语义。第二个是辅助任务和主要任务之间的优化不平衡问题。在本文中,我们提出了一种用于DDA预测的具有梯度平衡的新型异构图对比学习方法,即GCGB。为了应对第一个挑战,引入了融合视图来整合语义视图(药物和疾病相似性网络)和交互视图(异构生物医学网络)。接下来,设计视图间对比学习辅助任务,分别将融合视图与语义视图和交互视图进行对比。对于第二个挑战,我们从梯度方向和大小的角度自适应调整GCL辅助任务的梯度,以便更好地引导参数更新朝着主要任务进行。在10折交叉验证下的三个基准上进行的大量实验证明了该模型的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/dcd5c851c3d6/bbae650f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/f16e8a30fcb5/bbae650f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/13fe80326dbf/bbae650f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/90416c1795be/bbae650f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/dcd5c851c3d6/bbae650f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/f16e8a30fcb5/bbae650f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/13fe80326dbf/bbae650f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/90416c1795be/bbae650f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf32/11653209/dcd5c851c3d6/bbae650f4.jpg

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Nat Rev Neurol. 2024 Apr;20(4):245-251. doi: 10.1038/s41582-024-00940-4. Epub 2024 Feb 29.
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Fusing graph transformer with multi-aggregate GCN for enhanced drug-disease associations prediction.将图变换与多聚合 GCN 融合,用于增强药物-疾病关联预测。
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