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机构地区:[1]武汉大学人民医院生殖医学中心,武汉430060
出 处:《中国性科学》2017年第12期34-37,共4页Chinese Journal of Human Sexuality
基 金:中央高校基本科研业务费专项资金青年教师资助项目(2042017kf0073)
摘 要:目的:探讨MIF、COX-2与子宫内膜异位症(endometriosis,EM)的相关性研究。方法:采用免疫组织化学的方法测定EM患者49例异位内膜、40例在位的内膜及对照组正常内膜40例中MIF、COX-2的表达,并进行相关性分析。结果:(1)MIF、COX-2在EM在位内膜、异位内膜的表达率明显高于正常对照组,比较有统计学意义(P<0.01)。(2)异位和在位的内膜组中,MIF、COX-2表达在Ⅲ~Ⅳ期均高于Ⅰ~Ⅱ期,比较有统计学的意义(P<0.05)。(3)异位和在位的内膜组中,MIF表达与COX-2的表达呈正相关性(P<0.05)。结论:MIF可能通过增加COX-2表达而促进EM的发生、发展。Objectives: To study the expression of MIF and COX-2 in endometriosis( EM) and the correlation between MIF,COX-2 and EM. Methods: MIF and COX-2 expression was detected by immunohistochemistry methods in 40 cases of eutopic endometrium and 49 cases of ectopic endometrium and 40 cases of normal endometium. The results were analyzed statistically. Results:( 1) The positive expression rate MIF and COX-2 in eutopic and ectopic endometrium were much higher than those in control group( P 0. 01).( 2) In the stage III/IV,the expression of MIF and COX-2 in eutopic and ectopic endometrium were much higher than these in stage I/II( P 0. 05).( 3) The expression of MIF was shown to be significantly correlated to COX-2( P 0. 01).Conclusion: The expression of MIF is significantly correlated to the expression of COX-2 in ectopic and eutopic endometriosis,which may play a crucial role in the pathogenesis on endometriosis.
关 键 词:子宫内膜异位症 巨噬细胞移动抑制因子 环氧化酶-2
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