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子宫内膜癌组织COX-2和VEGF及KDR蛋白表达临床意义的探讨 被引量:2

Expressions of COX-2,VEGF and KDR protein and their clinical significance in endometrial carcinoma tissues
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摘要 目的:分析子宫内膜癌组织COX-2、VEGF和KDR蛋白的表达及临床意义。方法:应用免疫组化法对112例子宫内膜癌组织COX-2、VEGF和KDR蛋白进行检测。结果:112例子宫内膜癌组织COX-2、VEGF和KDR蛋白的阳性率分别为47.32%、66.07%和52.68%,三者表达具有协同性。Ⅱ+Ⅲ+Ⅳ期子宫内膜癌组织COX-2、VEGF和KDR蛋白表达阳性率分别为68%、88%和72%,高于Ⅰ期41.38%、59.77%和47.13%,P<0.05。低分化子宫内膜癌组织COX-2和VEGF蛋白表达阳性率100%,高于中分化61.11%和69.44%以及高分化的29.69%和57.81%,P<0.05。肌层浸润>1/2子宫内膜癌组织COX-2、VEGF和KDR蛋白表达阳性率62.5%、96.88%和84.38%,高于肌层浸润≤1/2者41.25%、53.75%和40%,P<0.05。结论:COX-2、VEGF和KDR蛋白在子宫内膜癌织中的表达水平均较高且具有协同性。COX-2、VEGF及KDR是参与肿瘤发生、发展和转移的重要基因。 OBJECTIVE: To analyze the expressions of COX-2,VEGF and KDR protein in endometrial carcinoma in order to find their clinical significance.METHOD:The immunohistochemical method was used to detect the expressions of COX-2,VEGF and KDR protein.RESULTS: The expression rates were 47.32% for COX-2 detected,66.07% for VEGF detected and 52.68% for KDR detected respectively in 112 patients with endometrial carcinoma.The positive rates of COX-2,VEGF and KDR protein expressions in operative stage Ⅱ+Ⅲ+Ⅳ(68%,88% and 72%) were statistically higher than those in stage Ⅰ(41.38%,59.77% and 47.13%,P〈0.05).The positive rates of COX-2,VEGF protein expression in poorly differentiated group(100% and 100%) were statistically higher than those in moderately and well differentiated groups(61.11% and 29.69%;69.44% and 57.81%,P〈0.05).The positive rates of COX-2,VEGF and KDR protein expressions in myometrial invasion 〉1/2(62.5%,96.88% and 84.38%) were statistically higher than those in ≤1/2(41.25%,53.75%,40%,P〈0.05).CONCLUSIONS: The expressions of COX-2,VEGF and KDR protein in endometrial carcinoma are high.COX-2,VEGF and KDR are important genes in the carcinogenesis,development and metastasis of endometrial carcinoma.
出处 《中华肿瘤防治杂志》 CAS 2009年第22期1782-1785,共4页 Chinese Journal of Cancer Prevention and Treatment
关键词 子宫内膜肿瘤 前列腺素内过氧化物合酶 血管内皮生长因子类 免疫组织化学 endometrial neoplasms prostaglandin endoperoxide synthase vascular endothelial growth factor immunohistochemistry
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