The role of EP-2 receptor expression in cervical intraepithelial neoplasia

Histochem Cell Biol. 2020 Dec;154(6):655-662. doi: 10.1007/s00418-020-01909-2. Epub 2020 Aug 26.

Abstract

Prostaglandin induced signalling is involved in different cancers. As previously described, the EP3 receptor expression decreases with increasing stage of cervical intraepithelial lesions (CIN). In addition, in cervical cancer EP3 is an independent prognosticator for overall survival and correlates with FIGO stages. Currently the role of Prostaglandin 2 receptor 2 (EP2) in CIN is unknown. The aim of this study was to analyse the expression of EP2 for potential prognostic value for patients with cervical dysplasia. EP2 expression was analysed by immunohistochemistry in 33 patient samples (CIN1-3) using the immune-reactivity scoring system (IRS). Expression levels were correlated with clinical outcome to analyse prognostic relevance in patients with CIN2. Data analysis was performed using non parametric Kruskal-Wallis and Spearman rank sum test. Cytoplasmic expression levels of EP2 correlated significantly (p < 0.001) with different grades of cervical dysplasia. Median EP2-IRS in CIN1 was 2 (n = 8), 3 in CIN2 (n = 9) and 6 in CIN3 (n = 16). Comparing regressive (n = 3, median IRS = 2) to progressive (n = 6, median IRS = 4) CIN2 cases the median IRS differed significantly (p = 0.017). Staining intensity (p = 0.009) and IRS (p = 0.005) of EP2 and EP3 correlate inversely. EP2 expression level significantly increases with higher grade of CIN and could qualify as a potential prognostic marker for the regressive or progressive course in CIN2 lesions. These findings emphasize the significant role of PGE2 signalling in CIN and could help to identify targets for future therapies.

Keywords: CIN; Cervical cancer HPV; Cervical intraepithelial neoplasia; EP-receptor; EP2; Prostaglandin E2.

MeSH terms

  • Biomarkers, Tumor / analysis
  • Biomarkers, Tumor / biosynthesis*
  • Biomarkers, Tumor / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Prognosis
  • Receptors, Prostaglandin E, EP2 Subtype / analysis
  • Receptors, Prostaglandin E, EP2 Subtype / biosynthesis*
  • Receptors, Prostaglandin E, EP2 Subtype / metabolism
  • Uterine Cervical Dysplasia / diagnosis
  • Uterine Cervical Dysplasia / metabolism*
  • Uterine Cervical Neoplasms / diagnosis
  • Uterine Cervical Neoplasms / metabolism*

Substances

  • Biomarkers, Tumor
  • PTGER2 protein, human
  • Receptors, Prostaglandin E, EP2 Subtype