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来曲唑在子宫内膜异位症治疗中的作用 被引量:2

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摘要 目的通过观察芳香化酶抑制剂-来曲唑作用于体外培养的子宫内膜异位症患者在位内膜细胞(Ectopic endometrial cells of women with endometriosis,EE)后芳香化酶及芳香化酶转录刺激因子-类固醇源性因子(SF-1)的表达情况,探讨来曲唑作为芳香化酶抑制剂对子宫内膜异位症(内异症)的作用。方法以0、0.1、1、10、100 nmol/L浓度的来曲唑对体外培养的子宫内膜异位症者的在位内膜细胞(EE)分别进行刺激。72 h后采用RT-PCR法从核酸水平检测Aromatase和SF-1的mRNA表达情况。结果不同浓度的来曲唑均可明显抑制细胞内Aromatasem RNA及SF-1mRNA表达,与空白组比较有显著性差异(P<0.05);且抑制作用呈浓度依赖性。结论芳香化酶抑制剂-来曲唑对内异症在位内膜细胞具有明显抑制EE细胞内芳香化酶及其转录调节因子SF-1的与mRNA表达。
作者 庞丽娜
机构地区 锦州市妇婴医院
出处 《中国医药指南》 2014年第8期107-108,共2页 Guide of China Medicine
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