A Dynamic Multi-Scale Hypergraph Learning Framework Driven by Features and Structures for ceRNA-Disease Association Prediction
Competitive endogenous RNA (ceRNA) networks are pivotal for uncovering disease molecular mechanisms. Graph representation learning is a cornerstone for modeling biological regulatory networks and predicting disease-related biomarkers. However, current methods face challenges: traditional graph neural network (GNN) rely on low-order graph structures, which struggle to capture high-order molecular interactions, resulting in topological information loss; shallow GNN fail to model long-range dependencies, while deep architectures suffer from over-smoothing, limiting complex regulatory expression; static embeddings overlook dynamic molecular interactions, reducing biomarker accuracy. These limitations highlight the need for advanced graph learning frameworks. To address these challenges, we propose DMHLF, a Dynamic Multi-scale Hypergraph Learning Framework for predicting disease-associated ceRNA biomarkers. The framework first integrates multiple regulatory relationships among miRNAs, lncRNAs, circRNAs, mRNAs, and diseases to construct disease-specific ceRNA regulatory networks, capturing local and global regulatory patterns through multi-Hop hyperedges. Subsequently, we devise a Hypergraph-Weighted Dynamic Random Walk (HEDRW) method to dynamically extract node meta-embeddings that encode high-order regulatory information. Concurrently, we extend Eigen-GNN spectral analysis to hypergraph structures, incorporating a residual-enhanced hypergraph neural network to preserve the global topological properties of shallow hypergraphs. Finally, a cross-scale attention mechanism aligns and fuses multi-scale features to generate high-quality node embeddings for disease-ceRNA association prediction. Experiments on diverse datasets demonstrate that DMHLF significantly outperforms existing methods. Case study further validates the framework's efficacy in identifying disease-related ceRNA biomarkers, providing a reliable predictive tool for biomedical research.
Authors
- Renchu Guan (ORCID: https://orcid.org/0000-0002-7162-7826)
- Zhu‐Hong You (ORCID: https://orcid.org/0000-0003-1266-2696)
- Fengfeng Zhou (ORCID: https://orcid.org/0000-0002-8108-6007)
- Xinfei Wang
- Yan Wang (ORCID: https://orcid.org/0000-0002-4751-0708)
- Yuqing Li (ORCID: https://orcid.org/0000-0002-5110-4323)
- Lan Huang (ORCID: https://orcid.org/0000-0003-3233-3777)
- Yuan Fu
Institutions
- Aberystwyth University (GB)
- Northwestern Polytechnical University (CN)
- University of Toronto (CA)
- Jilin University (CN)
- Jilin Province Science and Technology Department (CN)
- Institute of Biological, Environmental and Rural Sciences (GB)
Publication Details
- Journal
- IEEE Journal of Biomedical and Health Informatics
- Published
- 2025-08-25
- DOI
- https://doi.org/10.1109/jbhi.2025.3602670
- Citations
- 2
- Primary Topic
- Cancer-related molecular mechanisms research
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- Jilin Scientific and Technological Development Program