Di Carlo Costantino, Bonifacio Marika, Tommaselli Giovanni A, Bifulco Giuseppe, Guerra Germano, Nappi Carmine
Department of Obstetrics and Gynecology, University of Naples Federico II, Naples, Italy.
Fertil Steril. 2009 Jun;91(6):2315-23. doi: 10.1016/j.fertnstert.2008.03.079. Epub 2008 Jul 21.
To evaluate the expression of vascular endothelial growth factor (VEGF), angiopoietin 1 and 2 (ANGPT1/ANGPT2), and matrix metalloproteinases 1, 2, and 9 (MMP-1, MMP-2, MMP-9) in eutopic and ectopic endometrium.
Experimental retrospective study.
University hospital.
PATIENT(S): Eutopic and ectopic endometrium samples from 30 women with endometriosis and endometrium biopsy samples from 30 healthy women.
INTERVENTION(S): Biopsies of ovarian endometriomas and eutopic endometrium.
MAIN OUTCOME MEASURE(S): Immunohistochemical staining to evaluate the expression of VEGF, ANGPT1, ANGPT2, MMP-1, MMP-2, and MMP-9, and real-time polymerase chain reaction analysis to quantify mRNA expression.
RESULT(S): Patients with endometriosis had higher levels of angiogenic factors and metalloproteinases in endometriotic cysts than in eutopic endometrium. These substances were also overexpressed in eutopic endometrium of patients with endometriosis when compared with normal controls.
CONCLUSION(S): Overexpression of angiogenic factors and metalloproteinases may be the characteristic feature of endometrium with greater potential to transform into endometriotic lesions in the peritoneal cavity. Structural and/or functional differences of eutopic endometrium could have a role in the pathogenesis of endometriosis secondary to the backward passage of endometrial cells into the peritoneal cavity. Whether these local factors may induce, promote, and/or regulate this transformation remains to be determined.
评估血管内皮生长因子(VEGF)、血管生成素1和2(ANGPT1/ANGPT2)以及基质金属蛋白酶1、2和9(MMP - 1、MMP - 2、MMP - 9)在在位内膜和异位内膜中的表达。
实验性回顾性研究。
大学医院。
30例子宫内膜异位症患者的在位内膜和异位内膜样本,以及30例健康女性的子宫内膜活检样本。
卵巢子宫内膜异位囊肿和在位内膜活检。
免疫组织化学染色评估VEGF、ANGPT1、ANGPT2、MMP - 1、MMP - 2和MMP - 9的表达,以及实时聚合酶链反应分析定量mRNA表达。
子宫内膜异位症患者的异位囊肿中血管生成因子和金属蛋白酶水平高于在位内膜。与正常对照相比,这些物质在子宫内膜异位症患者的在位内膜中也过度表达。
血管生成因子和金属蛋白酶的过度表达可能是具有更大潜力转化为腹腔内子宫内膜异位病变的内膜的特征。在位内膜的结构和/或功能差异可能在子宫内膜细胞逆行进入腹腔继发的子宫内膜异位症发病机制中起作用。这些局部因素是否可能诱导、促进和/或调节这种转化仍有待确定。