This study developed an 11-gene lymph node metastasis gene signature (LMGS) using an ensemble learning strategy to overcome the instability of traditional models and identifies SPIB as a molecular marker associated with lymphatic dissemination.
Abstract
Summary The heterogeneity within the same AJCC TNM stage of gastric cancer necessitates robust prognostic biomarkers beyond conventional staging. By integrating transcriptomic data from 1,613 patients across eight cohorts, we developed an 11-gene lymph node metastasis gene signature (LMGS) using an ensemble learning strategy to overcome the instability of traditional models. LMGS robustly predicted survival (mean C-index = 0.619), providing incremental prognostic value beyond conventional AJCC staging. Single-cell and spatial transcriptomic analyses revealed LMGS enrichment in epithelial/immune cells at the tumor-normal interface. Integrative analysis nominated the transcription factor SPIB as a candidate regulator, which was specifically overexpressed in metastatic lesions. Our study provides a clinically relevant prognostic tool and identifies SPIB as a molecular marker associated with lymphatic dissemination.
This study establishes a novel CSC–associated gene signature for diagnosis and prognosis in HCC and nominates belinostat as a repurposing candidate for targeting stemness‐related pathways, offering a promising strategy for personalized therapy.
Yang Zi, Ying Zhang, Jun Wu et al.· Stem Cells International· 0 citations
A dual-gene model based on neutrophil heterogeneity demonstrated strong predictive performance and functioned as an independent prognostic indicator, and distinct immune and prognostic differences were identified among molecular subtypes.
CENPM shows diametrically opposite expression–diameter relationships between N0 and N1 patients, suggesting a shift in biological behavior upon nodal involvement, with potential therapeutic relevance.
SIRPG is identified as an immune-related prognostic hub and context-dependent tumor-cell regulator associated with apoptosis, immune communication and spatial microenvironmental organization in HNSCC.
Jiaqi Tang, Yu-Lun He, Yu-Qi Wang et al.· Frontiers in Immunology· 0 citations
It is suggested that the stacking model holds promise as a noninvasive decision-support tool that may complement, rather than replace, current clinical staging practices, however, integration into clinical workflows requires prospective validation.
Xiaodong Liu, Fan Li, Ye Xiang et al.· npj Precision Oncology· 0 citations
An interpretable three-stage machine learning framework integrating mRNA, microRNA, DNA methylation, copy number variation, and protein expression data from The Cancer Genome Atlas that couples improved prognostic estimation with biological interpretability supporting multi-omics biomarker discovery in ovarian cancer.
Kosar Fateh, S. Sathipati· bioRxiv· 0 citations
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