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慢性苯中毒患者中拓扑异构酶 IIα 表达降低及拓扑异构酶 IIα 启动子的组蛋白和调控因子改变。

Decreased topoisomerase IIα expression and altered histone and regulatory factors of topoisomerase IIα promoter in patients with chronic benzene poisoning.

机构信息

Department of Hematology, First Affiliated Hospital, Wenzhou Medical College, Wenzhou, Zhejiang 325000, China.

出版信息

Toxicol Lett. 2011 Jun 10;203(2):111-7. doi: 10.1016/j.toxlet.2011.02.020. Epub 2011 Mar 5.

Abstract

Topoisomerase IIα (Topo IIα) has been implicated in the benzene-induced hemotoxicity in vitro. This study was to examine the effect of in vivo chronic benzene exposure on Topo IIα in human bone marrow mononuclear cells, and to further explore the mechanism underlying decreased Topo IIα expression in patients with chronic benzene exposure. Topo IIα activity, expression, and mRNA level assessed by DNA cleavage/relaxation assay, Western blot, and reverse transcriptase-PCR, decreased in patients with benzene exposure. These changes were accompanied by reduced histone H4 and H3 acetylation and H3K4 methylation, and increased H3K9 methylation in the Topo IIα promoter, which were evaluated by chromatin immunoprecipitation (ChIP) assay. In addition, there were alterations in mRNA levels of Topo IIα promoter regulatory factors such as SP1, ATF-2, SP3, NF-YA, NF-M, P53, C-MYB, C-JUN, and ICBP90. Our results demonstrate that Topo IIα expression was reduced in patients with chronic benzene exposure, which was accompanied by alterations in histone acetylation and methylation and regulatory factor mRNA levels of Topo IIα promoter.

摘要

拓扑异构酶 IIα(Topo IIα)已被牵连到体外苯诱导的血液毒性中。本研究旨在检测体内慢性苯暴露对人骨髓单核细胞中 Topo IIα 的影响,并进一步探讨慢性苯暴露患者中 Topo IIα 表达降低的机制。通过 DNA 切割/松弛测定、Western blot 和逆转录-聚合酶链反应评估,暴露于苯的患者中 Topo IIα 的活性、表达和 mRNA 水平降低。这些变化伴随着组蛋白 H4 和 H3 乙酰化和 H3K4 甲基化减少,以及 Topo IIα 启动子 H3K9 甲基化增加,这些变化通过染色质免疫沉淀(ChIP)检测评估。此外,Topo IIα 启动子调节因子如 SP1、ATF-2、SP3、NF-YA、NF-M、P53、C-MYB、C-JUN 和 ICBP90 的 mRNA 水平也发生了改变。我们的结果表明,慢性苯暴露患者的 Topo IIα 表达降低,伴随着组蛋白乙酰化和甲基化以及 Topo IIα 启动子调节因子 mRNA 水平的改变。

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