Cancer-associated fibroblast activation predicts progression, metastasis, and prognosis of cutaneous squamous cell carcinoma

Int J Cancer. 2024 Sep 15;155(6):1112-1127. doi: 10.1002/ijc.34957. Epub 2024 Apr 22.

Abstract

Cutaneous squamous cell carcinoma (cSCC) is the most common metastatic skin cancer and the metastatic disease is associated with poor prognosis. Cancer-associated fibroblasts (CAFs) promote progression of cancer, but their role in cSCC is largely unknown. We examined the potential of CAF markers in the assessment of metastasis risk and prognosis of primary cSCC. We utilized multiplexed fluorescence immunohistochemistry for profiling CAF landscape in metastatic and non-metastatic primary human cSCCs, in metastases, and in premalignant epidermal lesions. Quantitative high-resolution image analysis was performed with two separate panels of antibodies for CAF markers and results were correlated with clinical and histopathological parameters including disease-specific mortality. Increased stromal expression of fibroblast activation protein (FAP), α-smooth muscle actin, and secreted protein acidic and rich in cysteine (SPARC) were associated with progression to invasive cSCC. Elevation of FAP and platelet-derived growth factor receptor-β (PDGFRβ) expression was associated with metastasis risk of primary cSCCs. High expression of PDGFRβ and periostin correlated with poor prognosis. Multimarker combination defined CAF subset, PDGFRα-/PDGFRβ+/FAP+, was associated with invasion and metastasis, and independently predicted poor disease-specific survival. These results identify high PDGFRβ expression alone and multimarker combination PDGFRα-/PDGFRβ+/FAP+ by CAFs as potential biomarkers for risk of metastasis and poor prognosis.

Keywords: epidermolysis bullosa; fibroblast; metastasis; squamous cell carcinoma.

MeSH terms

  • Actins / metabolism
  • Aged
  • Biomarkers, Tumor / metabolism
  • Cancer-Associated Fibroblasts* / metabolism
  • Cancer-Associated Fibroblasts* / pathology
  • Carcinoma, Squamous Cell* / metabolism
  • Carcinoma, Squamous Cell* / pathology
  • Cell Adhesion Molecules / metabolism
  • Disease Progression*
  • Endopeptidases
  • Female
  • Gelatinases / metabolism
  • Humans
  • Male
  • Membrane Proteins* / metabolism
  • Middle Aged
  • Neoplasm Metastasis
  • Osteonectin / metabolism
  • Prognosis
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism
  • Receptor, Platelet-Derived Growth Factor beta* / metabolism
  • Serine Endopeptidases* / metabolism
  • Skin Neoplasms* / metabolism
  • Skin Neoplasms* / mortality
  • Skin Neoplasms* / pathology

Substances

  • fibroblast activation protein alpha
  • Serine Endopeptidases
  • Receptor, Platelet-Derived Growth Factor beta
  • Membrane Proteins
  • Biomarkers, Tumor
  • Gelatinases
  • Endopeptidases
  • Cell Adhesion Molecules
  • POSTN protein, human
  • Osteonectin
  • Receptor, Platelet-Derived Growth Factor alpha
  • PDGFRB protein, human
  • Actins