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Cross-talk between DNA methylation and active histone modifications regulates aberrant expression of ZAP70 in CLL

机译:DNA甲基化与活性组蛋白修饰之间的串扰调节CLL中ZAP70的异常表达

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摘要

Zeta-associated protein of 70 kD (ZAP70) is a recognized adverse prognostic marker in chronic lymphocytic leukaemia (CLL) associated with enhanced B-cell receptor signalling, significantly more aggressive disease course and poor overall survival. Zeta-associated protein of 70 kD is ordinarily expressed in T cells where it has a crucial role in T-cell receptor signalling, whereas its aberrant expression in CLL leads to enhanced B-cell receptor signalling and significantly more aggressive disease course. Although much is known about the activation of ZAP70 following engagement of T-cell receptor, there are little data on the regulation of ZAP70 gene expression in normal T cells or CLL. To understand the molecular events underpinning epigenetic regulation of ZAP70 gene in CLL, we have defined ZAP70 promoter region and outlined the regions crucial in regulating the gene activity. Following a direct comparison of ZAP70+ and ZAP70− primary CLLs, we show ZAP70 promoter in expressing CLLs to be associated with a spectrum of active histone modifications, some of which are tightly linked to aberrant DNA methylation in CLL. Cross-talk between histone modifications and reduced DNA methylation culminates in transcriptional de-repression of ZAP70. Moreover, treatment with histone deacetylase (HDAC) and DNA methylation inhibitors results in recovery of ZAP70 expression, which provides a possible explanation for the failure of HDAC inhibitors in CLL treatment and might serve as a cautionary warning for their future use in treatment of this leukaemia.
机译:70 kD的Zeta相关蛋白(ZAP70)是公认的慢性淋巴细胞白血病(CLL)不良预后标志物,与增强的B细胞受体信号传导,明显更具侵略性的疾病进程和较差的总体生存率有关。 70 kD的与Zeta相关的蛋白通常在T细胞中表达,在T细胞中它在T细胞受体信号传导中起关键作用,而它在CLL中的异常表达导致增强的B细胞受体信号传导和明显更具侵略性的疾病进程。尽管关于T细胞受体参与后ZAP70活化的了解很多,但有关正常T细胞或CLL中ZAP70基因表达调控的数据很少。为了了解CLL中ZAP70基因表观遗传调控的分子事件,我们定义了ZAP70启动子区域并概述了调控基因活性的关键区域。在直接比较ZAP70 +和ZAP70-初级CLL后,我们显示ZAP70启动子在表达CLL中与一系列活性组蛋白修饰相关,其中一些与组蛋白DNA甲基化紧密相关。组蛋白修饰和DNA甲基化降低之间的相互影响最终导致ZAP70的转录去阻遏。此外,用组蛋白脱乙酰基酶(HDAC)和DNA甲基化抑制剂治疗可恢复ZAP70表达,这为HDAC抑制剂在CLL治疗中失败提供了可能的解释,并可能为它们将来在治疗白血病中的使用提供警告。

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