A new immunohistochemical marker, insulinoma-associated protein 1 (INSM1), for Merkel cell carcinoma: Evaluation of 24 cases

Ann Diagn Pathol. 2019 Jun:40:53-58. doi: 10.1016/j.anndiagpath.2019.04.002. Epub 2019 Apr 11.

Abstract

Merkel cell carcinoma (MCC) is an uncommon primary neuroendocrine carcinoma of the skin. Nowadays, pathologists are required to perform immunohistochemistry to demonstrate neuroendocrine and epithelial differentiation for diagnosis of MCC. Insulinoma-associated protein 1 (INSM1) is a zinc-finger transcription factor expressed in tissues undergoing terminal neuroendocrine differentiation, and INSM1 immunohistochemistry is a well-validated nuclear marker of neuroendocrine differentiation. We evaluated 24 cases of MCC for the expression of INSM1 and compared it with frequently used neuroendocrine markers, Chromogranin A, Synaptophysin, and CD56. INSM1 was positive in all cases, and its expression was stronger, more extensive, clean and homogeneous compared to other markers. As a consequence, INSM1 can be used to serve as a solitary marker for neuroendocrine differentiation due to high sensitivity and specificity in MCC cases.

Keywords: CD56; Chromogranin; INSM1; Merkel cell carcinoma; Neuroendocrine carcinoma of the skin; Synaptophysin.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / metabolism*
  • CD56 Antigen / metabolism
  • Carcinoma, Merkel Cell / metabolism*
  • Carcinoma, Merkel Cell / pathology
  • Carcinoma, Neuroendocrine / metabolism*
  • Carcinoma, Neuroendocrine / pathology
  • Chromogranin A / metabolism
  • Female
  • Humans
  • Insulinoma / metabolism*
  • Insulinoma / pathology
  • Male
  • Middle Aged
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / pathology
  • Repressor Proteins / metabolism
  • Sensitivity and Specificity
  • Skin Neoplasms / metabolism*
  • Skin Neoplasms / pathology
  • Synaptophysin / metabolism
  • Transcription Factors / metabolism

Substances

  • Biomarkers, Tumor
  • CD56 Antigen
  • Chromogranin A
  • NCAM1 protein, human
  • Repressor Proteins
  • Synaptophysin
  • Transcription Factors
  • INSM1 protein, human