Multiparameter imaging reveals clinically relevant cancer cell-stroma interaction dynamics in head and neck cancer

Karolina Punovuori, Fabien Bertillot, Yekaterina A Miroshnikova, Mirjam I Binner, Satu-Marja Myllymäki, Gautier Follain, Kai Kruse, Johannes Routila, Teemu Huusko, Teijo Pellinen, Jaana Hagström, Noemi Kedei, Sami Ventelä, Antti Mäkitie, Johanna Ivaska, Sara A Wickström

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2 Citations (Scopus)
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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 languageEnglish
Pages (from-to)7267-7284.e20
JournalCell
Volume187
Issue number25
DOIs
Publication statusPublished - 12 Dec 2024
MoE publication typeA1 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

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