The role of DOG1 immunohistochemistry in dermatopathology

J Cutan Pathol. 2016 Nov;43(11):974-983. doi: 10.1111/cup.12787. Epub 2016 Sep 5.

Abstract

Background: This study was designed to evaluate the immunoexpression of DOG1, a specific marker expressed in gastrointestinal stromal tumors, in normal skin tissues and cutaneous epithelial tumors.

Methods: DOG1 immunostaining extent, intensity and pattern were evaluated in 69 cutaneous apocrine/eccrine tumors, 11 sebaceous tumors, 46 follicular tumors, 52 keratinocytic tumors and perilesional normal tissues.

Results: In normal tissues, DOG1 was expressed strongly in the intercellular canaliculi of eccrine glands, moderately in the myoepithelial cells of mammary and anogenital mammary-like glands, and weakly or not at all in the periphery of sebaceous lobules and the lower layer of epidermis and follicular infundibulum. All apocrine-type cutaneous mixed tumors showed apical-luminal positivity for DOG1, and 4/9 of these tumors included intercellular canaliculi highlighted by DOG1 immunostaining. Other sweat gland tumors, including hidrocystadenoma, spiradenoma, cylindroma and apocrine carcinoma, also expressed DOG1 focally with an apical-luminal pattern. Although slight membranous positivity for DOG1 was observed in various tumor types, hidradenoma papilliferum exhibited diffuse membranous DOG1 staining in the myoepithelial cells.

Conclusions: DOG1 is a novel marker for identifying intercellular canaliculi and is a potential immunomarker of myoepithelial cells specific to mammary glands, anogenital mammary-like glands and tumors originating therein.

Keywords: DOG1; eccrine differentiation; immunohistochemistry; intercellular canaliculi; skin.

MeSH terms

  • Anoctamin-1
  • Biomarkers, Tumor / metabolism
  • Chloride Channels / metabolism*
  • Diagnosis, Differential
  • Gastrointestinal Neoplasms / metabolism*
  • Gastrointestinal Stromal Tumors / metabolism*
  • Humans
  • Immunohistochemistry
  • Neoplasm Proteins / metabolism*
  • Skin / metabolism*
  • Skin Neoplasms / metabolism*

Substances

  • ANO1 protein, human
  • Anoctamin-1
  • Biomarkers, Tumor
  • Chloride Channels
  • Neoplasm Proteins