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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 highorder molecular interactions, resulting in topological information loss; shallow GNN fail to model long-range dependencies, while deep architectures suffer from oversmoothing, 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 HypergraphWeighted 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.
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http://dx.doi.org/10.1109/JBHI.2025.3602670 | DOI Listing |
Dev Growth Differ
September 2025
Laboratory for Epithelial Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
Multicellular organisms generate organizational complexity through morphogenesis, in which mechanical forces orchestrate the movements and deformations of cells and tissues, while chemical signals regulate the molecular events that generate and coordinate these forces. One common denominator that is critical both for mechanics and biochemistry is material property. Material properties define how materials deform or rearrange under applied forces, and how rapidly molecules interact or spread in space and time.
View Article and Find Full Text PDFIEEE Trans Neural Netw Learn Syst
September 2025
In industrial scenarios, semantic segmentation of surface defects is vital for identifying, localizing, and delineating defects. However, new defect types constantly emerge with product iterations or process updates. Existing defect segmentation models lack incremental learning capabilities, and direct fine-tuning (FT) often leads to catastrophic forgetting.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
College of Food Science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China; Fujian Provincial Key Laboratory of Quality Science and Processing Technology in Special Starch, Fujian Agriculture and Forestry University, Fuzhou, 350002, China; Key Laboratory of Subtropical Characteristic
The anti-digestive properties of cross-linked starches are essential for the development of low glycemic foods. Dynamic digestion modeling simulates the human digestive process more accurately and is an effective tool to study its anti-enzymatic mechanism. The structural evolution characteristics and the generation rules of sugar derivatives of lotus seed cross-linked starch with low, medium, high cross-linking degree (LS-2CS, LS-6CS, LS-12CS, respectively) were studied and compared during in vitro dynamic simulation digestive system.
View Article and Find Full Text PDFChemphyschem
September 2025
Department of Computer Science, Institute of Technology, Resource and Energy-efficient Engineering (TREE), Bonn-Rhein-Sieg University of Applied Sciences, 53757, Sankt Augustin, Germany.
Molecular modeling plays a vital role in many scientific fields, ranging from material science to drug design. To predict and investigate the properties of those systems, a suitable force field (FF) is required. Improving the accuracy or expanding the applicability of the FFs is an ongoing process, referred to as force-field parameter (FFParam) optimization.
View Article and Find Full Text PDFEnvironmental perturbations and local changes in cellular electric potential can stimulate cytoskeletal filaments to transmit ionic currents along their surface. Advanced models and accurate experiments may provide a molecular understanding of these processes and reveal their role in cell electrical activities. This article introduces a multi-scale electrokinetic model incorporating atomistic protein details and biological environments to characterize electrical impulses along microtubules.
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