Galectin-3 Expression in Benign and Malignant Skin Diseases With Epidermal Hyperplasia

Am J Dermatopathol. 2017 Oct;39(10):738-741. doi: 10.1097/DAD.0000000000000781.

Abstract

Galectin-3 has been suggested relative to tumor genesis, progression, and metastasis in basal cell carcinoma and squamous cell carcinoma that are the most common skin cancers characterized by malignant epidermal proliferation. In this study, we evaluated galectin-3 expression in seborrheic keratosis, keratoacanthoma, and infectious diseases including verruca vulgaris, condyloma acuminatum, and chromoblastomycosis that are pathologically featured by benign epidermal proliferation. Galectin-3 expression was shown by immunohistochemical staining and quantified using the Image Pro Plus V6.0. We found that galectin-3 distributed evenly in normal skin around the body decreased significantly in all selected diseases compared with healthy controls, but it was comparable among each disease. These findings imply that galectin-3 do not differentiate between benign and malignant proliferation of keratinocytes.

MeSH terms

  • Biomarkers / analysis*
  • Blood Proteins
  • Epidermis / metabolism
  • Epidermis / pathology
  • Galectin 3 / analysis
  • Galectin 3 / biosynthesis*
  • Galectins
  • Humans
  • Hyperplasia / metabolism
  • Hyperplasia / pathology
  • Keratinocytes / metabolism
  • Keratinocytes / pathology
  • Skin Diseases / metabolism*
  • Skin Diseases / pathology

Substances

  • Biomarkers
  • Blood Proteins
  • Galectin 3
  • Galectins
  • LGALS3 protein, human