Fusing graph transformer with multi-aggregate GCN for enhanced drug-disease associations prediction

被引:6
作者
He, Shihui [1 ,2 ]
Yun, Lijun [1 ,2 ]
Yi, Haicheng [3 ]
机构
[1] Yunnan Normal Univ, Sch Informat Sci & Technol, Kunming 650500, Peoples R China
[2] Engn Res Ctr Comp Vis & Intelligent Control Techno, Dept Educ, Kunming 650500, Peoples R China
[3] Northwestern Polytech Univ, Sch Comp Sci, Xian 710129, Peoples R China
关键词
Drug repositioning; Drug-disease associations; Graph transformer; Graph neural networks; Neural collaborative filtering;
D O I
10.1186/s12859-024-05705-w
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundIdentification of potential drug-disease associations is important for both the discovery of new indications for drugs and for the reduction of unknown adverse drug reactions. Exploring the potential links between drugs and diseases is crucial for advancing biomedical research and improving healthcare. While advanced computational techniques play a vital role in revealing the connections between drugs and diseases, current research still faces challenges in the process of mining potential relationships between drugs and diseases using heterogeneous network data.ResultsIn this study, we propose a learning framework for fusing Graph Transformer Networks and multi-aggregate graph convolutional network to learn efficient heterogenous information graph representations for drug-disease association prediction, termed WMAGT. This method extensively harnesses the capabilities of a robust graph transformer, effectively modeling the local and global interactions of nodes by integrating a graph convolutional network and a graph transformer with self-attention mechanisms in its encoder. We first integrate drug-drug, drug-disease, and disease-disease networks to construct heterogeneous information graph. Multi-aggregate graph convolutional network and graph transformer are then used in conjunction with neural collaborative filtering module to integrate information from different domains into highly effective feature representation.ConclusionsRigorous cross-validation, ablation studies examined the robustness and effectiveness of the proposed method. Experimental results demonstrate that WMAGT outperforms other state-of-the-art methods in accurate drug-disease association prediction, which is beneficial for drug repositioning and drug safety research.
引用
收藏
页数:18
相关论文
共 44 条
[1]  
Agarap A. F., 2018, arXiv, DOI DOI 10.48550/ARXIV.1803.08375
[2]   An overview of drug discovery and development [J].
Berdigaliyev, Nurken ;
Aljofan, Mohamad .
FUTURE MEDICINAL CHEMISTRY, 2020, 12 (10) :939-947
[3]  
Cai D, 2020, AAAI CONF ARTIF INTE, V34, P7464
[4]   Advancing Drug Discovery via Artificial Intelligence [J].
Chan, H. C. Stephen ;
Shan, Hanbin ;
Dahoun, Thamani ;
Vogel, Horst ;
Yuan, Shuguang .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2019, 40 (08) :592-604
[5]   NLLSS: Predicting Synergistic Drug Combinations Based on Semi-supervised Learning [J].
Chen, Xing ;
Ren, Biao ;
Chen, Ming ;
Wang, Quanxin ;
Zhang, Lixin ;
Yan, Guiying .
PLOS COMPUTATIONAL BIOLOGY, 2016, 12 (07)
[6]   Drug-target interaction prediction: databases, web servers and computational models [J].
Chen, Xing ;
Yan, Chenggang Clarence ;
Zhang, Xiaotian ;
Zhang, Xu ;
Dai, Feng ;
Yin, Jian ;
Zhang, Yongdong .
BRIEFINGS IN BIOINFORMATICS, 2016, 17 (04) :696-712
[7]   The computational prediction of drug-disease interactions using the dual-network L2,1-CMF method [J].
Cui, Zhen ;
Gao, Ying-Lian ;
Liu, Jin-Xing ;
Wang, Juan ;
Shang, Junliang ;
Dai, Ling-Yun .
BMC BIOINFORMATICS, 2019, 20 (1)
[8]   Exploiting drug-disease relationships for computational drug repositioning [J].
Dudley, Joel T. ;
Deshpande, Tarangini ;
Butte, Atul J. .
BRIEFINGS IN BIOINFORMATICS, 2011, 12 (04) :303-311
[9]  
Dwivedi VP, 2021, Arxiv, DOI arXiv:2012.09699
[10]   Matrix factorization-based data fusion for the prediction of lncRNA-disease associations [J].
Fu, Guangyuan ;
Wang, Jun ;
Domeniconi, Carlotta ;
Yu, Guoxian .
BIOINFORMATICS, 2018, 34 (09) :1529-1537