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Spatial single-cell analysis reveals tumor microenvironment signatures predictive of oral cavity cancer outcome.


ABSTRACT: Up to 20% of patients with early-stage oral squamous cell carcinoma (OSCC) develop postoperative relapse, but no parameters currently enable the identification of individuals with poor prognosis. Here, we report a spatially resolved single-cell analysis of the tumor microenvironment in OSCC. By analyzing >700,000 cells for 25 proteins using imaging mass cytometry, we discover leukocyte and endothelial cell phenotypes that are independent prognostic factors for survival. Most notably, the presence of proliferating lymphatic endothelial cells (KI67+PROX1+), which show distinct molecular signature in transcriptomic analyses, in the invasive tumor margin strongly predicts poor recurrence-free survival in early-stage OSCC. We validate our findings in an independent OSCC cohort using an easy-to-measure KI67+PROX1+ immunostaining biomarker assay and multivariate analyses of recurrence-free, disease-specific, and overall survival. Thus, our data highlight the role of tumor microenvironment in OSCC progression and its potential impact on treatment strategies.

SUBMITTER: Nasiaho J 

PROVIDER: S-EPMC12923947 | biostudies-literature | 2026 Feb

REPOSITORIES: biostudies-literature

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Spatial single-cell analysis reveals tumor microenvironment signatures predictive of oral cavity cancer outcome.

Näsiaho Joni J   Nissi Linda L   Ventelä Sami S   Irjala Heikki H   Salmi Marko M  

Cell reports. Medicine 20260201 2


Up to 20% of patients with early-stage oral squamous cell carcinoma (OSCC) develop postoperative relapse, but no parameters currently enable the identification of individuals with poor prognosis. Here, we report a spatially resolved single-cell analysis of the tumor microenvironment in OSCC. By analyzing >700,000 cells for 25 proteins using imaging mass cytometry, we discover leukocyte and endothelial cell phenotypes that are independent prognostic factors for survival. Most notably, the presenc  ...[more]

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