Neuroendocrine differentiation in head and neck squamous cell carcinoma

J Laryngol Otol. 2012 Dec;126(12):1261-70. doi: 10.1017/S0022215112002265. Epub 2012 Oct 11.

Abstract

Objective: Tumours with neuroendocrine differentiation frequently express chromogranin A, synaptophysin and somatostatin receptors. The role of neuroendocrine differentiation in head and neck squamous cell carcinoma is not yet clear.

Method: The presence of chromogranin A, synaptophysin and somatostatin receptors was studied immunohistochemically in 78 head and neck squamous cell carcinoma specimens.

Results: Sparse chromogranin A expression was found in 41 per cent, associated with high chromogranin A messenger RNA expression and the presence of dense core granules. Low synaptophysin expression was found in 18 per cent. The highest staining scores were found for somatostatin receptor 5 (82 per cent), followed by somatostatin receptor 1 (69 per cent) and somatostatin receptor 2 (54 per cent), whereas somatostatin receptors 3 and 4 expression was low. Expression was not correlated with tumour stage or survival.

Conclusion: Cells with neuroendocrine differentiation are sparsely scattered in some head and neck squamous cell carcinomas. Their pathophysiological role is elusive. In contrast, somatostatin receptor and particularly somatostatin receptor 5 expression is frequent in head and neck squamous cell carcinoma. Somatostatin receptor expression is not considered to indicate neuroendocrine differentiation in head and neck squamous cell carcinoma.

MeSH terms

  • Biomarkers, Tumor / metabolism*
  • Carcinoma, Squamous Cell / diagnosis*
  • Carcinoma, Squamous Cell / ultrastructure
  • Cell Transformation, Neoplastic / pathology
  • Cell Transformation, Neoplastic / ultrastructure
  • Chromogranin A / metabolism*
  • Female
  • Head and Neck Neoplasms / diagnosis*
  • Head and Neck Neoplasms / ultrastructure
  • Humans
  • Immunohistochemistry
  • Male
  • Microscopy, Electron, Transmission
  • Middle Aged
  • Receptors, Somatostatin / metabolism*
  • Synaptophysin / metabolism*

Substances

  • Biomarkers, Tumor
  • Chromogranin A
  • Receptors, Somatostatin
  • Synaptophysin