Eldafira Eldafira, A. Abinawanto, L. Sjahfirdi, Asmarinah Asmarinah, P. Soeharso, Muharam Muharam, V. Prasasty, D. Pujianto
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引用次数: 0
摘要
子宫内膜异位症是一种多因素疾病,遗传和环境因素相互作用导致其发病。本研究采用定量实时荧光定量PCR方法(Quantitative Real Time PCR)研究子宫内膜异位症患者雌激素受体α (ERα)和β (ERβ)在正常子宫内膜中的表达情况。此外,我们还采用酶联免疫吸附法测定了月经周期增殖期子宫内膜异位症患者血清雌二醇水平。子宫内膜异位症组ERβ mRNA表达量明显高于对照组,经t检验,差异有统计学意义(P<0.05)。子宫内膜异位症中ERβ的过度表达可能对子宫内膜异位症的病理有其他重要影响,使ERβ刺激子宫内膜异位症组织和细胞中前列腺素的产生。雌二醇含量与ERα表达不相关,与ERβ mRNA表达呈弱相关。分子对接分析表明,ERα和ERβ与合成抗雌激素药物具有不同的结合作用,其中Ral2对ERα和Aco1对ERβ的抑制作用最好。因此,这两种抑制剂可以作为进一步研究ERα, ERβ体外和体内抑制活性的先导。
Comparative study of estrogen receptor α, β mRNA expressions of endometriosis and normal endometrium in women and analysis of potential synthetic anti-estrogens in silico
Endometriosis is a multifactorial disease in which genetic and environmental factors interact causing its pathogenesis. The aim of this study was to investigate the expression pattern of estrogen receptor α (ERα) and β (ERβ) in endometriosis patients compared to normal endometrioum (n=18) as a control by using Quantitative Real Time PCR method. Moreover, we also measured serum estradiol levels of endometriosis patients in the proliferation phase of the menstrual cycle using the enzyme-linked immunosorbent assay method. The mRNA expression of ERβ was significantly higher in the endometriosis group compared to control, and the result of t-test showed that were significantly different (P<0.05). Overexpression of ERβ in endometriosis was likely to have other significant important impacts in the pathology of endometriosis that allowed ERβ to stimulate prostaglandin production in endometriosis tissue and cells. Estradiol content did not correlate with the ERα expression, and it is weakly correlated with ERβ mRNA expression. Molecular docking analysis showed that ERα and ERβ have different binding interactions with synthetic antiestrogens, whereas the best inhibitor was Ral2 to ERα and Aco1 to ERβ. Thus, both inhibitors could be used as leads in further investigation of ERα, ERβ inhibitory activities in vitro and in vivo.