Differential expression of CD44 in malignant cutaneous epithelial neoplasms

Am J Dermatopathol. 1995 Oct;17(5):447-51. doi: 10.1097/00000372-199510000-00003.

Abstract

The CD44 antigen (ECMRIII, Hermes antigen) is a highly glycosylated cell-surface polypeptide involved in diverse cellular functions, including cell adhesion and lymphocyte-homing receptor activity. CD44 is also expressed in vivo by several tumors, including astrocytomas, meningiomas, and colonic adenocarcinomas. In addition, it has been shown that expression of CD44 appears to confer metastatic potential to cell lines derived from certain adenocarcinomas. In the skin, CD44 is normally expressed in epidermal keratinocytes and hair follicular, sebaceous, and eccrine epithelial cells. However, there have been few data with regard to the expression in vivo of CD44 in primary cutaneous neoplasms. Furthermore, there have not been studies in vivo of the possible differential expression of CD44 in primary versus metastatic tumors in the skin. We have examined by immunohistochemistry the expression of CD44 in cutaneous invasive and metastatic squamous cell carcinomas, metastatic adenocarcinomas, and basal cell carcinomas. All invasive and metastatic squamous cell carcinomas, as well as metastatic adenocarcinomas, strongly expressed CD44; however, basal cell carcinomas were nonreactive or showed only focal, minimal reactivity. Adjacent normal skin demonstrated CD44 immunoreactivity throughout the epidermis, including the basal layer. In addition, hair follicles and sebaceous and eccrine glands expressed CD44. The results suggest that expression of CD44 in these cutaneous epithelial tumors is not related to malignant transformation, but instead may be related to tumor progression and the ability to metastasize.

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / secondary
  • Carcinoma, Basal Cell / genetics
  • Carcinoma, Basal Cell / secondary
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / secondary
  • Cell Adhesion / genetics
  • Disease Progression
  • Eccrine Glands / pathology
  • Epidermis / pathology
  • Epithelium / pathology
  • Gene Expression Regulation, Neoplastic*
  • Hair Follicle / pathology
  • Humans
  • Hyaluronan Receptors / genetics*
  • Immunohistochemistry
  • Keratinocytes / pathology
  • Neoplasm Invasiveness / genetics
  • Neoplasms, Glandular and Epithelial / genetics*
  • Neoplasms, Glandular and Epithelial / pathology
  • Receptors, Lymphocyte Homing / genetics
  • Sebaceous Glands / pathology
  • Skin / pathology
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology

Substances

  • Hyaluronan Receptors
  • Receptors, Lymphocyte Homing