Pseudogene Coexpression Networks Reveal a Robust Prognostic Signature for Pediatric B-ALL Survival

Risk classification in B-cell acute lymphoblastic leukemia (B-ALL) remains challenging, even in the era of genomic precision medicine. Current molecular classifiers fail to fully explain the heterogeneity in patient outcomes, suggesting that key regulatory layers remain hidden. In this study, we uncover a previously unexplored dimension of B-ALL biology by analyzing coexpression patterns between pseudogenes using single-sample coexpression networks (n = 1,416). Principal component analysis showed that these interactions explain a major component of variability among patients and contribute to patient stratification into clusters with distinct overall survival. After identifying interactions associated with these clusters, we used a LASSO-based feature selection pipeline to derive a three-interaction signature that predicted patient survival, with RPL7P10-RPS3AP36 emerging as the most robust biomarker. Our study shows that coexpression between pseudogenes represents a previously unrecognized layer of molecular heterogeneity in B-ALL, harboring promising molecular markers for future studies.

This study reveals pseudogene coexpression as a previously unrecognized driver of transcriptional heterogeneity in B-ALL. We identify robust survival biomarkers derived from these interactions and introduce a single-sample network framework that enables precise patient stratification and biomarker validation in independent cohorts.