Immunohistochemical detectability of cyclooxygenase-2 expression in cells of human melanocytic skin lesions: A methodological review

J Cutan Pathol. 2020 Apr;47(4):363-380. doi: 10.1111/cup.13606. Epub 2019 Dec 1.

Abstract

Increased cyclooxygenase-2 (COX-2) expression is thought to support tumorigenesis through various mechanisms and is analyzed as a potential cancer marker. In 18 studies, COX-2 expression in melanocytic lesions of human skin was examined immunohistochemically. However, results obtained by individual research groups differ in terms of detection frequency and level of this protein, as well as localization of stained cells within tumor. Possible reasons for the discrepancies are analyzed in this review: the application of different antibodies, the use of standard histopathological sections or tissue microarrays and the analyzes of staining results based on different algorithms. COX-2 level is significantly lower in nevi than in melanomas, increases gradually with progression of these malignant cancers and reaches the highest values in metastases. These gradual changes in COX-2 expression appear to be difficult to analyze based only on subjective assessment of staining intensity. The most convergent data were obtained using antibodies for N-terminal fragments of COX-2 protein and analyzing results based on calculation of percentage fraction of positive cells. The extent of stained area in specimen thus appears to be more important than the intensity of staining in terms of evaluation of COX-2 performance as a diagnostic and prognostic marker of cutaneous melanoma.

Keywords: cyclooxygenase-2 (COX-2); immunohistochemistry; marker; melanoma; nevus.

Publication types

  • Review

MeSH terms

  • Cyclooxygenase 2 / biosynthesis*
  • Gene Expression Regulation, Enzymologic*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Melanoma* / enzymology
  • Melanoma* / pathology
  • Melanoma, Cutaneous Malignant
  • Neoplasm Proteins / biosynthesis*
  • Skin Neoplasms* / enzymology
  • Skin Neoplasms* / pathology

Substances

  • Neoplasm Proteins
  • Cyclooxygenase 2
  • PTGS2 protein, human