生物
头颈部癌
基质
癌症
头颈部
癌症研究
遗传学
免疫学
医学
免疫组织化学
外科
作者
Karolina Punovuori,Fabien Bertillot,Yekaterina A. Miroshnikova,Madelaine Binner,Satu-Marja Myllymäki,Gautier Follain,Kai Kruse,Johannes Routila,Teemu Huusko,Teijo Pellinen,Jaana Hagström,Noémi Kedei,Sami Ventelä,Antti Mäkitie,Johanna Ivaska,Sara A. Wickström
出处
期刊:Cell
[Cell Press]
日期:2024-10-01
被引量:1
标识
DOI:10.1016/j.cell.2024.09.046
摘要
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.
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