Abstract
Epithelial tumors are characterized by abundant inter- and intra-tumor heterogeneity, which complicates diagnostics and treatment. The contribution of cancer-stroma interactions to this heterogeneity is poorly understood. Here, we report a paradigm to quantify phenotypic diversity in head and neck squamous cell carcinoma (HNSCC) with single-cell resolution. By combining cell-state markers with morphological features, we identify phenotypic signatures that correlate with clinical features, including metastasis and recurrence. Integration of tumor and stromal signatures reveals that partial epithelial-mesenchymal transition (pEMT) renders disease outcome highly sensitive to stromal composition, generating a strong prognostic and predictive signature. Spatial transcriptomics and subsequent analyses of cancer spheroid dynamics identify the cancer-associated fibroblast-pEMT axis as a nexus for intercompartmental signaling that reprograms pEMT cells into an invasive phenotype. Taken together, we establish a paradigm to identify clinically relevant tumor phenotypes and discover a cell-state-dependent interplay between stromal and epithelial compartments that drives cancer aggression.
Original language | English |
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Pages (from-to) | 7267-7284.e20 |
Journal | Cell |
Volume | 187 |
Issue number | 25 |
DOIs | |
Publication status | Published - 12 Dec 2024 |
MoE publication type | A1 Journal article-refereed |
Keywords
- Humans
- Epithelial-Mesenchymal Transition
- Head and Neck Neoplasms/pathology
- Stromal Cells/metabolism
- Cell Line, Tumor
- Squamous Cell Carcinoma of Head and Neck/metabolism
- Tumor Microenvironment
- Animals
- Cell Communication
- Mice
- Single-Cell Analysis
- Female
- Male
- Phenotype