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Differential Effects of Estradiol and Bisphenol A on SET8 and SIRT1 Expression in Ovarian Cancer Cells

机译:雌二醇和双酚A对卵巢癌细胞SET8和SIRT1表达的差异影响

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Exposure to estrogenic compounds has been shown to epigenetically reprogram the female reproductive tract and may contribute to ovarian cancer. The goal of this study was to compare the effect of estradiol or bisphenol A (BPA) on the expression of histone-modifying enzymes (HMEs) in ovarian cancer cells. Using 2 human ovarian cancer cell lines, we examined the expression of SET8 , a histone methyltransferase, and SIRT1 , a histone deacetylase, after exposure to estrogen or BPA. These experiments were carried out in complete media (fetal bovine serum) that contain natural hormones to understand the impact of additional exposure to estrogen or BPA on HME expression. We found differential expression of the HMEs in the different models examined and between the different compounds. Further, we determined that the changes in gene expression occurred via estrogen receptor signaling using the estrogen receptor antagonist, ICI 182,780 (fulvestrant).
机译:研究表明,暴露于雌激素化合物会表观遗传地重编程女性生殖道,并可能导致卵巢癌。这项研究的目的是比较雌二醇或双酚A(BPA)对卵巢癌细胞中组蛋白修饰酶(HMEs)表达的影响。使用2种人类卵巢癌细胞系,我们检测了暴露于雌激素或BPA后的组蛋白甲基转移酶SET8和组蛋白脱乙酰基酶SIRT1的表达。这些实验在包含天然激素的完全培养基(胎牛血清)中进行,以了解额外暴露于雌激素或BPA对HME表达的影响。我们在所检查的不同模型中以及不同化合物之间发现了HME的差异表达。此外,我们确定使用雌激素受体拮抗剂ICI 182,780(氟维司群)通过雌激素受体信号传导发生基因表达的变化。

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