Immunohistochemical localization of insulin-like growth factor-binding protein-3 in eutopic and ectopic endometrial tissues

Citation
A. Akoum et al., Immunohistochemical localization of insulin-like growth factor-binding protein-3 in eutopic and ectopic endometrial tissues, FERT STERIL, 72(6), 1999, pp. 1085-1092
Citations number
41
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
FERTILITY AND STERILITY
ISSN journal
00150282 → ACNP
Volume
72
Issue
6
Year of publication
1999
Pages
1085 - 1092
Database
ISI
SICI code
0015-0282(199912)72:6<1085:ILOIGF>2.0.ZU;2-W
Abstract
Objective: To evaluate the expression of insulin-like growth factor-binding protein-3 (IGFBP-3) in the eutopic endometrium and in endometriotic lesion s. Design: Retrospective immunohistochemical study. Patient(s): Twenty-five normal women and 39 women with endometriosis. Intervention(s): Endometrial and endometriotic tissue biopsies obtained at laparoscopy. Main Outcome Measure(s): Expression of IGFBP-3 assessed by immunohistochemi stry. Result(s): In the endometrium, positive immunostaining of IGFBP-3 was obser ved both in the stroma and the epithelial glands. The intensity of staining in the glands during the secretory phase was significantly higher in women with endometriosis compared with controls (P = .018). An increased express ion of IGFBP-3 over controls was found in stages I and II of the disease (P = .018), whereas in stages III and IV, the difference between controls and women with endometriosis was not significant (P = .300). In endometriotic tissues, a much-marked immunostaining of IGFBP-3 was noted in 90% of the gl ands and 67% of the stroma without apparent differences related to cycle ph ase. Conclusion(s): These data show intense staining of IGFBP-3 in endometriosis lesions and increased expression of the protein in the endometrium of pati ents with endometriosis compared to controls. This marked expression of IGF BP-3 could be related to its previous finding in the peritoneal fluid and t o its potential involvement in the pathophysiology of endometriosis. (C) 19 99 by American Society for Reproductive Medicine.