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Androgen receptor is negatively correlated with the methylation-mediated transcriptional repression of miR-375 in human prostate cancer cells

机译:雄激素受体与人类前列腺癌细胞中miR-375的甲基化介导的转录抑制负相关

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摘要

Androgen receptor (AR) plays a critical role during the development and progression of prostate cancer in which microRNA miR-375 is overexpressed and correlated with tumor progression. Although DNA methylation is a key mechanism for the repression of gene expression, the relationship between AR and the expression or the hypermethylation of miR-375 is unknown. In this study, we found that AR-positive prostate cancer (PCa) cells showed high expression levels and hypomethylation of the miR-375. In contrast, AR-negative PCa cells displayed low levels and hypermethylation of the miR-375. Addition of 5-Aza-2′-deoxycytidine, a specific inhibitor of DNA methylation, into the culture medium reversed the low expression levels of miR-375 in the AR negative PCa cells. In addition, the total activity levels of DNA methyltransferases (DNMTs) were high in AR-negative PCa cells, in which hypermethylation of miR-375 promoter and low expression levels of miR-375 were observed. Taken together, these findings indicate that the negative correlation between AR and total DNMT activity is one of mechanisms to influence the methylation status of miR-375 promoter, which in turn regulates the expression of miR-375.
机译:雄激素受体(AR)在前列腺癌的发展和进程中起着至关重要的作用,其中microRNA miR-375过度表达并与肿瘤进程相关。尽管DNA甲基化是抑制基因表达的关键机制,但AR与miR-375的表达或甲基化过度之间的关系尚不清楚。在这项研究中,我们发现AR阳性前列腺癌(PCa)细胞显示出miR-375的高表达水平和甲基化不足。相反,AR阴性的PCa细胞显示出低水平的miR-375甲基化。向培养基中添加5-甲基--2脱氧胞苷(一种DNA甲基化的特异性抑制剂)可逆转AR阴性PCa细胞中miR-375的低表达水平。此外,AR阴性PCa细胞中DNA甲基转移酶(DNMT)的总活性水平较高,其中观察到miR-375启动子超甲基化和miR-375的低表达水平。综上所述,这些发现表明AR与总DNMT活性之间的负相关性是影响miR-375启动子的甲基化状态的机制之一,其进而调节miR-375的表达。

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