Prognostic biomarker discovery via a connected network-constrained Cox proportional hazards model
Lingyu Li, Wai-Ki Ching, Zhi-Ping Liu

TL;DR
This paper introduces a new method for finding connected gene networks that predict breast cancer prognosis better than existing methods.
Contribution
The novel CNet-Cox model integrates network connectivity into survival analysis for more interpretable and robust biomarker discovery.
Findings
CNet-Cox identified connected prognostic genes in breast cancer with a concordance index of 0.913.
A six-gene prognostic risk score was validated across six external datasets and a spatial transcriptomic dataset.
The model outperformed traditional methods in patient stratification and biological interpretability.
Abstract
Biomarker discovery in biomedical sciences can be framed as feature selection in machine learning [1]. However, existing methods often overlook gene co-localization within regulatory interaction networks, leading to the identification of isolated biomarkers with limited biological interpretability [2]. Here, we present the Connected Network-regularized Cox proportional hazards model (CNet-Cox), which incorporates network connectivity constraints into sparse regularization to identify prognostic biomarkers for breast cancer (BRCA) on the discovery dataset from TCGA (1,092 patients), while explicitly accounting for patient survival time. CNet-Cox reveals the network structures of prognostic genes, evaluated in the internal validation dataset with a concordance index of 0.913, surpassing traditional regularized Cox methods. CNet-Cox shifts biomarker recognition from isolated to connected…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsBioinformatics and Genomic Networks · Ferroptosis and cancer prognosis · Computational Drug Discovery Methods
