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慢性淋巴细胞白血病预后亚组中基于全基因组芯片的差异甲基化图谱。

Differential genome-wide array-based methylation profiles in prognostic subsets of chronic lymphocytic leukemia.

机构信息

Department of Genetics and Pathology, Uppsala University, Uppsala, Sweden.

出版信息

Blood. 2010 Jan 14;115(2):296-305. doi: 10.1182/blood-2009-07-232868. Epub 2009 Nov 6.

Abstract

Global hypomethylation and regional hypermethylation are well-known epigenetic features of cancer; however, in chronic lymphocytic leukemia (CLL), studies on genome-wide epigenetic modifications are limited. Here, we analyzed the global methylation profiles in CLL, by applying high-resolution methylation microarrays (27,578 CpG sites) to 23 CLL samples, belonging to the immunoglobulin heavy-chain variable (IGHV) mutated (favorable) and IGHV unmutated/IGHV3-21 (poor-prognostic) subsets. Overall, results demonstrated significant differences in methylation patterns between these subgroups. Specifically, in IGHV unmutated CLL, we identified methylation of 7 known or candidate tumor suppressor genes (eg, VHL, ABI3, and IGSF4) as well as 8 unmethylated genes involved in cell proliferation and tumor progression (eg, ADORA3 and PRF1 enhancing the nuclear factor-kappaB and mitogen-activated protein kinase pathways, respectively). In contrast, these latter genes were silenced by methylation in IGHV mutated patients. The array data were validated for selected genes using methylation-specific polymerase chain reaction, quantitative reverse transcriptase-polymerase chain reaction, and bisulfite sequencing. Finally, the significance of DNA methylation in regulating gene promoters was shown by reinducing 4 methylated tumor suppressor genes (eg, VHL and ABI3) in IGHV unmutated samples using the methyl-inhibitor 5-aza-2'-deoxycytidine. Taken together, our data for the first time reveal differences in global methylation profiles between prognostic subsets of CLL, which may unfold epigenetic silencing mechanisms involved in CLL pathogenesis.

摘要

全球低甲基化和局部高甲基化是癌症中众所周知的表观遗传特征;然而,在慢性淋巴细胞白血病(CLL)中,对全基因组表观遗传修饰的研究有限。在这里,我们通过应用高分辨率甲基化微阵列(27578 个 CpG 位点)对 23 个 CLL 样本进行了 CLL 的全基因组甲基化谱分析,这些样本属于免疫球蛋白重链可变区(IGHV)突变(有利)和 IGHV 未突变/IGHV3-21(预后不良)亚组。总的来说,结果表明这些亚组之间的甲基化模式存在显著差异。具体来说,在 IGHV 未突变的 CLL 中,我们鉴定了 7 个已知或候选肿瘤抑制基因(如 VHL、ABI3 和 IGSF4)以及 8 个参与细胞增殖和肿瘤进展的未甲基化基因(如 ADORA3 和 PRF1,分别增强核因子-κB 和丝裂原激活蛋白激酶途径)的甲基化。相比之下,在 IGHV 突变的患者中,这些基因则因甲基化而沉默。使用甲基化特异性聚合酶链反应、定量逆转录聚合酶链反应和亚硫酸氢盐测序对选定基因的阵列数据进行了验证。最后,通过在 IGHV 未突变样本中使用甲基抑制剂 5-氮杂-2'-脱氧胞苷重新诱导 4 个甲基化肿瘤抑制基因(如 VHL 和 ABI3),显示了 DNA 甲基化在调节基因启动子中的重要性。总之,我们的数据首次揭示了 CLL 预后亚组之间全基因组甲基化谱的差异,这可能揭示了涉及 CLL 发病机制的表观遗传沉默机制。

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