Expression of Claudin-1 in laryngeal squamous cell carcinomas (LSCCs) and its significance

Histol Histopathol. 2021 Apr;36(4):437-446. doi: 10.14670/HH-18-320. Epub 2021 Feb 25.

Abstract

Background: A large body of scientific evidence points to the important roles of tight junction proteins in tumor development, progression and dissemination. The larynx has only a few studies, analyzing the role of this group of junctional proteins in its oncogenesis. In this study, the author sheds some light on the expression and possible role of claudin-1 in laryngeal squamous cell carcinomas.

Materials and methods: This study analyzed the expression of claudin-1, using immunohistochemistry, in a tissue microarray of 80 cases of laryngeal squamous cell cancers. Clinicopathological parameters were analyzed according to claudin-1 expression in the tissue microarray. Furthermore, the expression of slug/snail1, an Epithelial-Mesenchymal Transition (EMT) linked protein, was analyzed by immunohistochemistry in the same microarray, and the expressions of the two proteins were assessed for correlation.

Results: A significant majority of laryngeal squamous cell cancers exhibited positive expression of claudin-1 proteins. The majority of those tumors expressed claudin-1 in their cytoplasm. The overall majority of those same tumors also exhibited a cytoplasmic shift of the slug-snail-1 protein from the nuclei to the cytoplasm. There was also evidence of correlation of the two proteins' expressions in the cytoplasm of laryngeal tumors.

Conclusion: The above may suggest a role for claudin-1 in the development and progression of laryngeal squamous cell carcinoma. Overall, claudin-1's aberrant expression in laryngeal cancer is in line with evidence seen in other head and neck cancers. Its co-expression with slug/snail-1 in LSCC patients should be investigated further to understand the nature of the relationship of the two proteins in LSCC and their possible contribution to its development and progression.

MeSH terms

  • Biomarkers, Tumor / metabolism*
  • Cadherins / metabolism
  • Claudin-1 / metabolism*
  • Epithelial-Mesenchymal Transition
  • Gene Expression Regulation, Neoplastic
  • Head and Neck Neoplasms / metabolism
  • Head and Neck Neoplasms / pathology
  • Humans
  • Immunohistochemistry
  • Laryngeal Neoplasms* / metabolism
  • Laryngeal Neoplasms* / pathology
  • Snail Family Transcription Factors / metabolism
  • Squamous Cell Carcinoma of Head and Neck* / metabolism
  • Squamous Cell Carcinoma of Head and Neck* / pathology

Substances

  • Biomarkers, Tumor
  • Cadherins
  • Claudin-1
  • Snail Family Transcription Factors