DNA hypomethylation of the nuclear receptor subfamily 5 (NR5A1) gene promoter is associated with endometriosis among women in north west of Iran

Soraya Larki, M. Maleki
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Abstract

Background and objectives: Endometrial tissue growth and its activity outside the uterus cause endometriosis. It has been suggested that various epigenetic deviations play a major role in the pathogenesis of endometriosis. Steroidogenic factor 1 (SF-1; NR5A1) is an essential transcription factor for estrogen biosynthesis in endometrial cells. The expression of SF-1 in endometriosis and lack of expression in normal endometrium is primarily determined by its promoter methylation. Here, we aimed to compare the methylation status of the SF-1 gene promoter region in women with endometriosis in comparison to healthy subjects. Methods: In the present case–control study, DNA was extracted from 25 endometrial tissue samples from women with endometriosis and 5 normal post-hysterectomy endometrium tissues which were collected from Tabriz hospitals including Vali-e-Asr, Taleghani, 29 Bahman and Shams in 2016. The obtained DNA samples were subjected to Bisulfite-treatment. Finally, the status of SF1gene promoter methylation was evaluated by methylation specific PCR method. Statistical analyses including descriptive and inferential statistics were conducted using tables, bar charts by statistical software SPSS version 20 and independence test. Results: The methylation status of SF-1 gene promoter was decreased significantly in endometriosis samples (P<0.05). Conclusion: SF-1 gene promoter hypomethylation could increase the relative expression of SF-1 gene in endometriosis which may lead to the development or progression of the disease.
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核受体亚家族5 (NR5A1)基因启动子的DNA低甲基化与伊朗西北部女性子宫内膜异位症有关
背景与目的:子宫内膜组织生长及其在子宫外的活动可引起子宫内膜异位症。各种表观遗传偏差在子宫内膜异位症的发病机制中起重要作用。甾体生成因子1 (SF-1;NR5A1)是子宫内膜细胞雌激素生物合成的重要转录因子。SF-1在子宫内膜异位症中的表达和在正常子宫内膜中的表达缺失主要是由其启动子甲基化决定的。在这里,我们的目的是比较SF-1基因启动子区域的甲基化状态在子宫内膜异位症妇女与健康受试者的比较。方法:选取2016年在大不里士(Tabriz) Vali-e-Asr、Taleghani、29 Bahman和Shams等医院采集的子宫内膜异位症患者子宫内膜样本25份和子宫切除术后正常子宫内膜样本5份,进行病例对照研究。得到的DNA样品进行亚硫酸氢盐处理。最后,采用甲基化特异性PCR方法评价sf1基因启动子甲基化状态。统计分析包括描述性统计和推断性统计,采用SPSS version 20统计软件,采用表格、柱状图进行统计分析,并进行独立性检验。结果:SF-1基因启动子甲基化状态在子宫内膜异位症中显著降低(P<0.05)。结论:SF-1基因启动子低甲基化可增加SF-1基因在子宫内膜异位症中的相对表达,可能导致疾病的发生或进展。
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