Aug 2026· Proceedings of the 32nd ACM SIGKDD Conference on Knowledge Discovery and Data Mining V.2· pp. 11480-11491· 0 citations· 58 references
TL;DR
LaCONIC is proposed, a label-aware and graph-guided multi-omics collaborative learning framework that bridges fine-grained molecular regulation and coarse-grained patient prognosis and consistently outperforms 14 representative survival baselines.
Abstract
Accurate cancer survival prediction is important for risk stratification and personalized treatment. However, patient prognosis is shaped by complex molecular regulation, cross-omics dependencies, and subtype-dependent tumor heterogeneity, making accurate and interpretable prediction challenging. Existing multi-omics survival models often treat omics profiles mainly as feature views and learn coarse patient-level representations, leaving fine-grained gene regulatory topology and subtype-structured prognostic heterogeneity underexploited. We propose LaCONIC, a label-aware and graph-guided multi-omics collaborative learning framework that bridges fine-grained molecular regulation and coarse-grained patient prognosis. LaCONIC first learns topology-aware gene structural representations through heterogeneous regulatory graph pretraining on a multi-entity disease gene regulatory network. It then performs adaptive cross-omics representation learning for intra-omics expression-graph fusion and inter-omics alignment, followed by ceRNA-guided attention to model miRNA-mRNA-lncRNA interactions under biological priors. During training, LaCONIC requires subtype annotations and leverages them through subtype classification and multi-level contrastive constraints to preserve subtype-dependent survival heterogeneity and improve risk-discriminative representation learning. Experiments across multiple TCGA cancer datasets demonstrate that LaCONIC consistently outperforms 14 representative survival baselines, while SHAP-based analyses identify prognosis-associated regulatory modules and biomarkers.
Cancer subtype classification based on molecular features is important for characterizing tumor heterogeneity, evaluating patient prognosis, and supporting precision treatment. Multi-omics integration provides complementary molecular information across genomic, epigenomic, transcriptomic, and proteomic levels. Howeve...
Ke Wang, Jin-Bo Zheng, Lu-Lu Zhao et al.· BMC Bioinformatics· 0 citations
A biologically informed cross-omics attention mechanism is deployed to explicitly model directional regulatory dependencies, enabling inter-omics information exchange aligned with known molecular hierarchies and enabling the identification of female-associated prognostic biomarkers that were overlooked in prior mixed-s...
Zi-Xiao Lu, Jia-Jun Wang, Yu-Ping Liang et al.· Briefings in Bioinformatics· 0 citations
To provide accurate and helpful insights, healthcare early illness risk prediction requires the integration of diverse multi-omics data. Unlike existing models (MOGONet, ExplainMix, CNNs), X-GCN presents an integrated explainable graph-based framework that combines graph convolution with hierarchical attention in a uni...
Suresh Kulandaivelu, Mohan Mani· Natural Resources for Human...· 0 citations
Cancer continues to be a significant worldwide health concern, mostly resulting from modifications in genetic material at the molecular level. The research introduces a hybrid system that integrates raw gene-level multi-omics features with pathway-derived hypergraph embeddings to prioritize glioblastoma genes. The prop...
Nowsheena, Shaima Qureshi· Computational biology and ch...· 0 citations
Cancer subtype identification from multi-omics profiles is important for understanding tumor heterogeneity and advancing computational precision oncology. Various subtyping methods have been proposed, among which graph-based approaches have become a widely adopted paradigm by capturing patient-to-patient relationships...
Findings show that patient-graph construction is a key design choice in pan-cancer multi-omics learning and that leakage-controlled evaluation is essential for reliable and biologically informative benchmarking in computational oncology.