A context-aware multi-task heterogeneous graph neural network (GNN) for predicting ncRNA associations with cancer types and metastatic events and enables context-specific prioritization of ncRNA–cancer–metastasis associations for experimental evaluation.
Abstract
Metastasis involves context-dependent molecular interactions in which non-coding RNAs, particularly miRNAs and circRNAs, play important regulatory roles. However, existing computational approaches generally do not jointly represent cancer type, metastatic event, and cancer-specific metastatic context. We developed a context-aware multi-task heterogeneous graph neural network (GNN) for predicting ncRNA associations with cancer types and metastatic events. The framework integrates multiple biological repositories into a heterogeneous graph representing ncRNAs, cancers, metastatic event types (METs), and cancer-specific metastatic instances (CSMIs). The model performs six link-prediction tasks using a hierarchical transformer-based encoder and multi-relational TuckER decoder. Across ten independently initialized runs evaluated on the RNA-group-disjoint held-out test set, the model achieved a global AUROC of 0.8801 ± 0.0118 and an F1 score of 0.8260 ± 0.0071. All three ablation variants yielded lower AUROC, with the largest reduction under independent task training. Case studies in pancreatic cancer, colorectal cancer, and hepatocellular carcinoma provided disease-level, event-level, and expression-based support, respectively, for top-ranked candidate associations. The framework enables context-specific prioritization of ncRNA–cancer–metastasis associations for experimental evaluation.
This approach efficiently decodes the complex interactive topologies between lncRNAs and human diseases through topology-aware network representation and equilibrium-driven distribution alignment and provides more effective theoretical guidance for interpreting lncRNA-mediated cellular control systems and discovering p...
Jia-Jia Liu, Mu-Gang Lin, Ling-ling Zhu et al.· Bio Systems· 0 citations
This chapter provides a comprehensive technical protocol for predicting CDGs using a Graph Convolutional Network (GCN) and guides the reader through hyperparameter optimization, model training, and performance evaluation, while discussing practical considerations related to generalization, computational cost, and inter...
Renan Soares de Andrades, M. Recamonde-Mendoza· Methods in molecular biology· 0 citations
RGCNMDA is a leakage-controlled multi-view framework that integrates global latent structure, local profiles and similarities, and pathway context that supports the robustness of leakage-controlled multi-view learning across standard and cold-start evaluation settings.
Chao Hou, Mohamed Kone, Yang Xiang et al.· Bioinformatics· 0 citations
Accumulating evidence suggests that long noncoding RNAs (lncRNAs) interact synergistically with diverse cellular molecules to regulate a wide range of biological processes. Identifying lncRNA-disease associations (LDAs) is therefore essential for elucidating disease mechanisms and advancing biomarker discovery. Althoug...
Liu-Jian Ni, Qing-Yang Liu, Hong-Jiu Liu et al.· Computational biology and ch...· 0 citations
Breast cancer drug resistance remains a major clinical challenge driven by complex genetic, signaling, and microenvironmental interactions. Conventional machine learning and deep learning represent genes, drugs, and patients as independent feature vectors, limiting their ability to capture biological relationships gove...
Priyanshu Das, Md. Jarifur Rahman, Sowhanur Rahman Nirob et al.· Frontiers in Oncology· 0 citations
Experimental results show that MVGSCA effectively integrates heterogeneous biological information and achieves superior prediction performance, offering valuable insights into cancer resistance mechanisms and supporting drug discovery efforts.
Ru Nie, Ying Fu, Zheng-Wei Li et al.· IEEE transactions on computa...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.