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小B细胞淋巴瘤中基因启动子的差异性DNA甲基化

Differential DNA methylation of gene promoters in small B-cell lymphomas.

作者信息

Guo Juyuan, Burger Matthias, Nimmrich Inko, Maier Sabine, Becker Evelyne, Genc Buelent, Duff Dieter, Rahmatpanah Farahnaz, Chitma-Matsiga Rebecca, Shi Huidong, Berlin Kurt, Huang Tim H-M, Caldwell Charles W

机构信息

Department of Pathology and Anatomical Sciences, University of Missouri School of Medicine, Columbia 65203, USA.

出版信息

Am J Clin Pathol. 2005 Sep;124(3):430-9. doi: 10.1309/LCGN-V77J-464L-NFD6.

Abstract

Improved care of patients with small B-cell lymphomas (SBCLs) is likely to result from the ongoing discovery of molecular markers that better define these malignant neoplasms. We identified multiple gene loci whose DNA methylation patterns differed between 3 types of SBCL: B-cell chronic lymphocytic leukemia/small lymphocytic lymphoma, mantle cell lymphoma, and grades I and II follicular lymphoma. This analysis was performed using an oligonucleotide microarray that allowed determination of the DNA methylation status of 156 loci in 38 genes. Combined bisulfite restriction analysis and methylation-specific polymerase chain reaction were used to validate the differential methylation of 6 of these genes. By using non-Hodgkin lymphoma cell lines as models, these genes were examined further for methylation and gene expression relationships. This study illustrates nonrandom epigenetic alterations in SBCLs that seem to preferentially involve lymphomas of germinal center derivation.

摘要

对小B细胞淋巴瘤(SBCL)患者护理的改善可能源于不断发现能更好地界定这些恶性肿瘤的分子标志物。我们鉴定出多个基因位点,其DNA甲基化模式在3种SBCL之间存在差异:B细胞慢性淋巴细胞白血病/小淋巴细胞淋巴瘤、套细胞淋巴瘤以及I级和II级滤泡性淋巴瘤。该分析使用了一种寡核苷酸微阵列,可测定38个基因中156个位点的DNA甲基化状态。采用联合亚硫酸氢盐限制分析和甲基化特异性聚合酶链反应来验证其中6个基因的差异甲基化。通过使用非霍奇金淋巴瘤细胞系作为模型,进一步研究了这些基因的甲基化与基因表达之间的关系。这项研究表明SBCL中存在非随机的表观遗传改变,这些改变似乎优先涉及生发中心来源的淋巴瘤。

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