›› 2011, Vol. 42 ›› Issue (3): 378-383.doi: 10.3969/j.issn.0529-1356.2011.03.017

• 论著 • 上一篇    下一篇

血管内皮生长因子、Eph受体酪氨酸激酶A2、基质金属蛋白酶-2和-9在卵巢癌血管生成拟态中的作用

王立1 ;王俊艳1* ;赵秀兰2;赵楠2 ;张丹芳2;孙保存2   

  1. 1.天津医科大学组织学与胚胎学教研室; 2.病理学教研室,天津 300070
  • 收稿日期:2010-09-12 修回日期:2010-11-05 出版日期:2011-06-06
  • 通讯作者: 王俊艳

Effects of vascular endothelial growth factor,Eph receptor A2, matrix metalloproteinase-2 and -9 in ovarian carcinoma vasculogenic mimicry

  1. 1. Department of Histology and Embryology, Tianjin Medical University; 2. Department of Pathology, Tianjin Medical University, Tianjin 300070,China
  • Received:2010-09-12 Revised:2010-11-05 Online:2011-06-06
  • Contact: WANG Jun-yan

关键词: 卵巢癌, 血管生成拟态, 血管内皮生长因子, Eph受体酪氨酸激酶A2, 基质金属蛋白酶, 免疫组织化学,

Abstract: Objective To investigate the effect of vascular endothelial growth factor (VEGF), Eph receptor A2(EphA2), matrix metalloproteinases(MMP)-2 and MMP-9 in ovarian carcinoma vasculogenic mimicry(VM). Methods Totally 84 ovarian carcinoma specimens with complete clinical and prognostic data were collected, and using CD31 and PAS double staining to confirm if vasculogenic mimicry exists in the ovarian carcinoma specimens. Immunohistochemical method was used to detect VEGF, EphA2, MMP-2 and MMP-9, examining the results of the immunohistochemical method according to the dye index. Results VEGF, EphA2 and MMP-9 in ovarian carcinoma specimens had significant differences between the VM group (36/84) and non-VM group (48/84), the expression in the VM group showed significantly higher than that in non-VM group. But the expression of MMP-2 between the two groups was not statistically significant. BR> Conclusion Vasculogenic mimicry and endothelium-derived angiogenesis are co-existed in ovarian carcinoma, VEGF, EphA2 and MMP-9 play important roles in vasculogenic mimicry. Detecting VEGF, EphA2 and MMP-9 can be used to evaluate the prognosis of ovarian carainoma. BR>

Key words: Ovarian carcinoma, Vasculogenic mimicry, Vascular endothelial growth factor, Eph receptor A2, Matrix metalloproteinase, Immunohistochemistry, Human

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