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. 2013 Apr;121(1):35-40.
doi: 10.1016/j.ijgo.2012.10.025. Epub 2013 Jan 16.

Analysis of biomarker expression in severe endometriosis and determination of possibilities for targeted intraoperative imaging

Liseth L van den Berg  1 , Lucia M A Crane, Marleen van Oosten, Gooitzen M van Dam, Arnold H M Simons, H Sijbrand Hofker, Joost Bart
Affiliations

Analysis of biomarker expression in severe endometriosis and determination of possibilities for targeted intraoperative imaging

Liseth L van den Berg et al. Int J Gynaecol Obstet. 2013 Apr.

Abstract

Objective: To evaluate the expression of biomarkers in endometriotic tissue in order to determine the most promising molecules for targeted intraoperative imaging.

Methods: Tissue samples were obtained from 18 patients with endometriosis. The intensity and pattern of expression of the following biomarkers were assessed by immunohistochemistry: C-X-C chemokine receptor type 4 (CXCR4), epithelial cell adhesion molecule (EpCAM), estrogen receptor (ER), folate receptor α (FR-α), hypoxia-inducible factor 1-α (HIF-1α), progesterone receptor (PR), and vascular endothelial growth factor A (VEGF-A). The Target Selection Criteria scoring system was used to select the most promising biomarkers for intraoperative imaging.

Results: Expression of CXCR4, EpCAM, ER, PR, and VEGF-A was scored as strong in endometriotic epithelium. Expression of FR-α was detected in 94.4% of samples, whereas HIF-1α was expressed in just 5.6% of samples. Of note, CXCR4, ER, and VEGF-A were also expressed in surrounding healthy tissue, thus reducing the target-to-background ratio.

Conclusion: Of the 7 biomarkers assessed in the present study, EpCAM, FR-α, and VEGF-A seem the most promising for targeted intraoperative imaging of endometriosis.

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