Prediction of drug–disease associations by integrating common topologies of heterogeneous networks and specific topologies of subnets

Author:

Gao Ling1,Cui Hui2,Zhang Tiangang3,Sheng Nan4,Xuan Ping1

Affiliation:

1. School of Computer Science and Technology, Heilongjiang University, Harbin 150080, China

2. Department of Computer Science and Information Technology, La Trobe University, Melbourne 3083, Australia

3. School of Mathematical Science, Heilongjiang University, Harbin 150080, China

4. College of Computer Science and Technology, Jilin University, Changchun 130012, China

Abstract

Abstract Motivation The development process of a new drug is time-consuming and costly. Thus, identifying new uses for approved drugs, named drug repositioning, is helpful for speeding up the drug development process and reducing development costs. Existing drug-related disease prediction methods mainly focus on single or multiple drug–disease heterogeneous networks. However, heterogeneous networks, and drug subnets and disease subnet contained in heterogeneous networks cover the common topology information between drug and disease nodes, the specific information between drug nodes and the specific information between disease nodes, respectively. Results We design a novel model, CTST, to extract and integrate common and specific topologies in multiple heterogeneous networks and subnets. Multiple heterogeneous networks composed of drug and disease nodes are established to integrate multiple kinds of similarities and associations among drug and disease nodes. These heterogeneous networks contain multiple drug subnets and a disease subnet. For multiple heterogeneous networks and subnets, we then define the common and specific representations of drug and disease nodes. The common representations of drug and disease nodes are encoded by a graph convolutional autoencoder with sharing parameters and they integrate the topological relationships of all nodes in heterogeneous networks. The specific representations of nodes are learned by specific graph convolutional autoencoders, respectively, and they fuse the topology and attributes of the nodes in each subnet. We then propose attention mechanisms at common representation level and specific representation level to learn more informative common and specific representations, respectively. Finally, an integration module with representation feature level attention is built to adaptively integrate these two representations for final association prediction. Extensive experimental results confirm the effectiveness of CTST. Comparison with six latest methods and case studies on five drugs further verify CTST has the ability to discover potential candidate diseases.

Funder

Natural Science Foundation of China

Natural Science Foundation of Heilongjiang Province

China Postdoctoral Science Foundation

Heilongjiang Postdoctoral Scientific Research Staring Foundation

Fundamental Research Foundation of Universities in Heilongjiang Province for Technology Innovation

Innovation Talents Project of Harbin Science and Technology Bureau

Fundamental Research Foundation of Universities in Heilongjiang Province for Youth Innovation Team

Foundation of Graduate Innovative Research

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A Survey of Deep Learning for Detecting miRNA- Disease Associations: Databases, Computational Methods, Challenges, and Future Directions;IEEE/ACM Transactions on Computational Biology and Bioinformatics;2024-05

2. GCNGAT: Drug–disease association prediction based on graph convolution neural network and graph attention network;Artificial Intelligence in Medicine;2024-04

3. Subgraph-Aware Dynamic Attention Network for Drug Repositioning;Lecture Notes in Computer Science;2024

4. Hierarchical Semantic Augmentation Graph Neural Network for Drug-Disease Association Prediction;2023 IEEE International Conference on Bioinformatics and Biomedicine (BIBM);2023-12-05

5. A Survey of Computational Methods and Databases for lncRNA-MiRNA Interaction Prediction;IEEE/ACM Transactions on Computational Biology and Bioinformatics;2023-09-01

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3