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Int J Clin Exp Pathol ; 7(11): 7752-9, 2014.
Article in English | MEDLINE | ID: mdl-25550812

ABSTRACT

Angiogenesis is an important pathogenesis of Endometriosis. Vascular endothelial growth factor C (VEGF-C) is one of the most important factor in the regulation of both normal and abnormal angiogenesis. Anti-angiogenic treatment of endometriosis is still in the exploratory stage. In this study, we investigate the relationship between VEGF-C and endometriosis, the therapeutic effects of Endostar in the rat endometriosis model. We then demonstrated that Immunohistochemical expression of VEGF-C was higher in endometriotic tissues than in control normal ovary tissues (P < 0.01) and higher in the endomertriosis grade III-IV than in endomertriosis grade I-II (P=0.013). In rat endometriosis model, we observed a significant reduction in the mean volume and weight of the endometriotic implants per rat in the treatment group as compared with the control group. By immunohistochemical evaluation, there was a significant reduction in VEGF-C expression after treatment in all areas examined. VEGF-C may be involved in the pathogenesis of endomertriosis by regulating the angiogenesis. Endostar has therapeutic effects of endometriosis lesions in the rat endometriosis model.


Subject(s)
Endometriosis/metabolism , Endometrium/metabolism , Neovascularization, Pathologic/metabolism , Vascular Endothelial Growth Factor C/metabolism , Adult , Animals , Disease Models, Animal , Endometriosis/drug therapy , Endometriosis/pathology , Endometrium/drug effects , Endometrium/pathology , Endostatins/pharmacology , Endostatins/therapeutic use , Female , Humans , Middle Aged , Neovascularization, Pathologic/drug therapy , Neovascularization, Pathologic/pathology , Rats , Recombinant Proteins , Young Adult
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