Single-cell transcriptomic profiling and machine learning identify S-nitrosylation-associated LAMC2 as a key prognostic driver in pancreatic cancer
Year: 2025
Type: article
Abstract: BACKGROUND: Pancreatic cancer (PC) remains one of the deadliest malignancies worldwide, characterized by late diagnosis, limited therapeutic options, and dismal prognosis. Post-translational modifications (PTMs) are increasingly recognized as key regulators of tumor biology, yet the role of S-nitrosylation-a redox-based cysteine modification-has not been systematically investigated in PC. METHODS: We integrated bulk and single-cell transcriptomic data from TCGA, ICGC, and GEO cohorts to comprehensively profile S-nitrosylation-related gene expression. A large-scale machine-learning framework incorporating 101 algorithmic combinations was used to construct an optimized prognostic model. Kaplan-Meier, ROC, and PCA analyses evaluated predictive power and stability across nine independent cohorts. The key hub gene LAMC2 was identified and subjected to single-gene bioinformatic analysis and functional validation through in-vitro experiments using MIA-PaCa-2 cells. RESULTS: S-nitrosylation exhibited the highest enrichment among all PTM types in pancreatic cancer and was mainly localized to malignant ductal and fibroblast cells. The StepCox(backward) + GBM model showed excellent prognostic performance (TCGA C-index = 0.827) and successfully stratified patients into high- and low-risk groups across multiple external datasets. High-risk patients displayed distinct transcriptional profiles and significantly worse survival outcomes (all p < 0.01). Among S-nitrosylation-related genes, LAMC2 showed the strongest correlation with risk score (r = 0.63) and was consistently upregulated in tumors. Cox and GSEA analyses linked LAMC2 to epithelial-mesenchymal transition, TGF-β, and hypoxia pathways. Functionally, LAMC2 knockdown suppressed migration and colony formation in pancreatic cancer cells. CONCLUSIONS: This study establishes S-nitrosylation as a crucial PTM in pancreatic cancer and introduces a robust machine-learning-based prognostic model. LAMC2 is identified as a key oncogenic effector connecting S-nitrosylation dysregulation to tumor aggressiveness, providing novel prognostic and therapeutic insights for pancreatic cancer management.
Source: Discover Oncology
Authors: Chenchen Yang, Hengfa Ge, Yunfan Yin, Jialing Zhang, Aifeng Gong
Institutions: Huaian First People’s Hospital, Nanjing Medical University
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,690
OpenAlex ID: W4417537338