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肾透明细胞肉瘤中存在异常的表观遗传调控,其特征为明显的DNA高甲基化和EZH2过表达。

Aberrant epigenetic regulation in clear cell sarcoma of the kidney featuring distinct DNA hypermethylation and EZH2 overexpression.

作者信息

Karlsson Jenny, Valind Anders, Jansson Caroline, O'Sullivan Maureen J, Holmquist Mengelbier Linda, Gisselsson David

机构信息

Department of Clinical Genetics, Lund University, University and Regional Laboratories, Lund, Sweden.

National Children's Research Centre, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.

出版信息

Oncotarget. 2016 Mar 8;7(10):11127-36. doi: 10.18632/oncotarget.7152.

Abstract

The global methylation profile and the mutational status of 633 specific epigenetic regulators were analyzed in the pediatric tumor clear cell sarcoma of the kidney (CCSK). Methylation array analyses of 30 CCSKs revealed CCSK tumor DNA to be globally hypermethylated compared to Wilms tumor, normal fetal kidney, and adult kidney. The aberrant methylation pattern of CCSKs was associated with activation of genes involved in embryonic processes and with silencing of genes linked to normal kidney function. No epigenetic regulator was recurrently mutated in our cohort, but a mutation in the key epigenetic regulator EZH2 was discovered in one case. EZH2 mRNA was significantly higher in CCSK compared to Wilms tumor and normal kidney, and the EZH2 protein was strongly expressed in more than 90 % of CCSK tumor cells in 9/9 tumors analyzed. This was in striking contrast to the lack of EZH2 protein expression in Wilms tumor stromal elements, indicating that EZH2 could be explored further as a diagnostic marker and a potential drug target for CCSK.

摘要

对633个特定表观遗传调节因子的整体甲基化谱和突变状态进行了分析,研究对象为小儿肿瘤肾透明细胞肉瘤(CCSK)。对30例CCSK进行甲基化阵列分析发现,与肾母细胞瘤、正常胎儿肾脏和成人肾脏相比,CCSK肿瘤DNA整体呈高甲基化状态。CCSK异常的甲基化模式与胚胎发育相关基因的激活以及与正常肾功能相关基因的沉默有关。在我们的队列中,没有表观遗传调节因子发生复发性突变,但在1例病例中发现关键表观遗传调节因子EZH2发生了突变。与肾母细胞瘤和正常肾脏相比,CCSK中EZH2 mRNA显著更高,在分析的9/9例肿瘤中,超过90%的CCSK肿瘤细胞中EZH2蛋白强烈表达。这与肾母细胞瘤基质成分中缺乏EZH2蛋白表达形成鲜明对比,表明EZH2可作为CCSK的诊断标志物和潜在药物靶点进行进一步研究。

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