Translational Oncology· 2026Q1
Single-cell spatial transcriptomics identifies SERPINE1 as a vascular endothelial mediator of cisplatin resistance in head and neck squamous cell carcinoma
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- Q1SCImago
- 2026year
Short summary
Single-cell and spatial transcriptomics reveal SERPINE1, upregulated in tumor endothelial cells, as a key mediator of cisplatin resistance in head and neck squamous cell carcinoma (HNSCC), particularly in HPV-negative tumors.
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Key points
- Cisplatin resistance signals are enriched in tumor endothelial cells, particularly in HPV-negative HNSCC.
- SERPINE1 is identified as a key endothelial gene associated with cisplatin resistance, showing upregulation and correlation with resistance scores.
- High SERPINE1 expression is linked to poor patient survival and an immunosuppressive tumor microenvironment.
- SERPINE1-high HNSCC tumors show predicted sensitivity to EGFR/SRC- and MAPK-pathway inhibitors.
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Abstract
Background Cisplatin resistance remains a major obstacle in head and neck squamous cell carcinoma (HNSCC), yet the contribution of the vascular microenvironment and its variation across HPV statuses remains unclear. Methods We integrated single-cell RNA sequencing, spatial transcriptomics, and bioinformatics analyses to characterize cisplatin resistance-associated cellular states in HNSCC. Cisplatin resistance scoring, pseudotime analysis, transcriptional regulatory network analysis, and cell–cell communication analysis were used to identify resistant subpopulations. Spatial localization, survival analysis, immune infiltration assessment, and drug sensitivity prediction were further performed to evaluate key candidate genes. Results Cisplatin resistance signals were preferentially enriched in tumor endothelial cells and were stronger in HPV-negative HNSCC. Endothelial cells with high resistance scores exhibited enhanced angiogenesis, extracellular matrix remodeling, hypoxia, and inflammatory programs. Multidimensional screening identified SERPINE1 as a key resistance-associated endothelial gene, showing significant upregulation and positive correlation with resistance scores. Single-cell and spatial transcriptomic analyses consistently demonstrated vascular-associated enrichment of SERPINE1, particularly in HPV-negative tumors. High SERPINE1 expression was associated with poor survival and an immunosuppressive tumor microenvironment. Drug sensitivity prediction suggested increased sensitivity of SERPINE1-high tumors to EGFR/SRC- and MAPK-pathway inhibitors, whereas no significant differences were observed for conventional cytotoxic agents. Conclusion SERPINE1 defines a tumor endothelial state associated with cisplatin resistance in HNSCC and may contribute to HPV-related differences in the vascular microenvironment, providing a potential basis for therapeutic stratification.
The authors' abstract, as published at the source. Translational Oncology, 2026 · DOI ↗
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Field: Otorhinolaryngology
OtorhinolaryngologyMedicine