AI Article Synopsis

  • Prostaglandin signaling, specifically through the EP3 receptor, shows decreased expression with advanced stages of cervical intraepithelial lesions (CIN), affecting overall survival.
  • The current study focuses on the EP2 receptor in 33 patient samples, finding that higher EP2 expression significantly correlates with increased grades of cervical dysplasia.
  • Results suggest that EP2 may serve as a prognostic marker for determining whether CIN2 lesions will regress or progress, highlighting the importance of PGE2 signaling in cervical cancer treatment strategies.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723936PMC
http://dx.doi.org/10.1007/s00418-020-01909-2DOI Listing

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