There is a suggested pathogenetic role of cyclooxygenase-2 (COX-2) in endometriosis via angiogenesis and proproliferative mechanisms. The aim of the study was to investigate the immunohistochemical COX-2 expression in different anatomical sites of endometriosis and its correlation to proliferative activity and periendometriotic vascularization. Sixty endometrioses from different sites (ovarian, uterine, and peritoneal) were evaluated immunohistochemically for COX-2 expression. Cyclooxygenase-2 staining of 75\% or more of the cells was defined as COX-2 overexpression and used as cutoff. Proliferative activity was determined by performing Ki-67-labeling index. Periendometriotic vascularization was evaluated by determining microvessel density surrounding the endometriotic focus using CD-34-immunostaining. Cyclooxygenase-2 overexpression was significant more frequent in ovarian endometriosis, when compared with uterine and peritoneal localization (70.8\% versus 41.7\%; P = .027). There was no significant correlation between COX-2 overexpression and perifocal neovascularization (P = .49). Endometriotic lesions with COX-2 overexpression represented reduced proliferative activity (P = .055). Cyclooxygenase-2 is expressed in the majority of endometriosis, but differences exist within the frequency of overexpression at different anatomical sites of the endometriosis. Cyclooxygenase-2 inhibitors are of clinical interest as treatment options.
%0 Journal Article
%1 Horn.2009
%A Horn, Lars-Christian
%A Hentschel, Bettina
%A Meinel, Alexandra
%A Alexander, Henry
%A Leo, Cornelia
%D 2009
%J Annals of diagnostic pathology
%K Cell_Proliferation Chi-Square_Distribution Cyclooxygenase_2/metabolism Endometriosis/metabolism/pathology Female Humans Immunohistochemistry Ki-67_Antigen/metabolism Neovascularization,_Pathologic/metabolism Ovarian_Diseases/metabolism/pathology Peritoneal_Diseases/metabolism/pathology Statistics,_Nonparametric Uterine_Diseases/metabolism/pathology
%N 6
%P 373–377
%T Cyclooxygenase-2 expression, Ki-67 labeling index, and perifocal neovascularization in endometriotic lesions
%V 13
%X There is a suggested pathogenetic role of cyclooxygenase-2 (COX-2) in endometriosis via angiogenesis and proproliferative mechanisms. The aim of the study was to investigate the immunohistochemical COX-2 expression in different anatomical sites of endometriosis and its correlation to proliferative activity and periendometriotic vascularization. Sixty endometrioses from different sites (ovarian, uterine, and peritoneal) were evaluated immunohistochemically for COX-2 expression. Cyclooxygenase-2 staining of 75\% or more of the cells was defined as COX-2 overexpression and used as cutoff. Proliferative activity was determined by performing Ki-67-labeling index. Periendometriotic vascularization was evaluated by determining microvessel density surrounding the endometriotic focus using CD-34-immunostaining. Cyclooxygenase-2 overexpression was significant more frequent in ovarian endometriosis, when compared with uterine and peritoneal localization (70.8\% versus 41.7\%; P = .027). There was no significant correlation between COX-2 overexpression and perifocal neovascularization (P = .49). Endometriotic lesions with COX-2 overexpression represented reduced proliferative activity (P = .055). Cyclooxygenase-2 is expressed in the majority of endometriosis, but differences exist within the frequency of overexpression at different anatomical sites of the endometriosis. Cyclooxygenase-2 inhibitors are of clinical interest as treatment options.
@article{Horn.2009,
abstract = {There is a suggested pathogenetic role of cyclooxygenase-2 (COX-2) in endometriosis via angiogenesis and proproliferative mechanisms. The aim of the study was to investigate the immunohistochemical COX-2 expression in different anatomical sites of endometriosis and its correlation to proliferative activity and periendometriotic vascularization. Sixty endometrioses from different sites (ovarian, uterine, and peritoneal) were evaluated immunohistochemically for COX-2 expression. Cyclooxygenase-2 staining of 75\% or more of the cells was defined as COX-2 overexpression and used as cutoff. Proliferative activity was determined by performing Ki-67-labeling index. Periendometriotic vascularization was evaluated by determining microvessel density surrounding the endometriotic focus using CD-34-immunostaining. Cyclooxygenase-2 overexpression was significant more frequent in ovarian endometriosis, when compared with uterine and peritoneal localization (70.8\% versus 41.7\%; P = .027). There was no significant correlation between COX-2 overexpression and perifocal neovascularization (P = .49). Endometriotic lesions with COX-2 overexpression represented reduced proliferative activity (P = .055). Cyclooxygenase-2 is expressed in the majority of endometriosis, but differences exist within the frequency of overexpression at different anatomical sites of the endometriosis. Cyclooxygenase-2 inhibitors are of clinical interest as treatment options.},
added-at = {2014-10-15T15:03:55.000+0200},
author = {Horn, Lars-Christian and Hentschel, Bettina and Meinel, Alexandra and Alexander, Henry and Leo, Cornelia},
biburl = {https://www.bibsonomy.org/bibtex/25b215e7701ca8d4cde38320bc622e9a5/drtester},
interhash = {35c75790776c880a362999a4d9ac532b},
intrahash = {5b215e7701ca8d4cde38320bc622e9a5},
journal = {Annals of diagnostic pathology},
keywords = {Cell_Proliferation Chi-Square_Distribution Cyclooxygenase_2/metabolism Endometriosis/metabolism/pathology Female Humans Immunohistochemistry Ki-67_Antigen/metabolism Neovascularization,_Pathologic/metabolism Ovarian_Diseases/metabolism/pathology Peritoneal_Diseases/metabolism/pathology Statistics,_Nonparametric Uterine_Diseases/metabolism/pathology},
number = 6,
pages = {373–377},
timestamp = {2014-10-15T15:03:55.000+0200},
title = {Cyclooxygenase-2 expression, Ki-67 labeling index, and perifocal neovascularization in endometriotic lesions},
volume = 13,
year = 2009
}