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甲基化导致弥漫性大B细胞淋巴瘤中PRDM1α/PRDM1bβ表达失衡。

Methylation contributes to imbalance of PRDM1α/PRDM1bβ expression in diffuse large B-cell lymphoma.

作者信息

Zhang Yi-Wen, Zhang Jie, Li Jun, Zhu Jun-Feng, Yang Yan-Li, Zhou Li-Li, Hu Zhong-Li, Zhang Feng

机构信息

a Department of Hematology , The First Affiliated Hospital of Bengbu Medical College , Bengbu , Anhui Province , China.

b Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Key Laboratory of Thrombosis and Hemostasis of Ministry of Health , Suzhou , Jiangsu Province , China.

出版信息

Leuk Lymphoma. 2015;56(8):2429-38. doi: 10.3109/10428194.2014.994181. Epub 2015 Jan 21.

Abstract

The positive regulatory domain 1 (PRDM1) exists as two isoforms: PRDM1α and PRDM1β. The former is frequently inactivated, while the latter is overexpressed in a subset of diffuse large B-cell lymphoma (DLBCL). To investigate the possible epigenetic alteration of PRDM1α and PRDM1β expression, the methylation of these two promoter isoforms was assessed in B lymphoma cell lines and DLBCL samples. Hypomethylation of PRDM1β CpG islands was preferentially detected in lymphoma cells. However, both high and low methylation of PRDM1α CpG islands was simultaneously observed in cases of DLBCL compared with the moderate methylation of non-tumor cases. CpG 16-21-specific high methylation was correlated with low expression of PRDM1α in PRDM1β-positive DLBCL samples. Three increased and one decreased miRNAs were significantly different between cases of DLBCL and non-tumor reactive hyperplasia. Thus, our results indicate that aberrant methylation silencing of PRDM1α and hypomethylation activation of PRDM1β are frequent events in DLBCL.

摘要

正调控结构域1(PRDM1)以两种异构体形式存在:PRDM1α和PRDM1β。前者常被失活,而后者在一部分弥漫性大B细胞淋巴瘤(DLBCL)中过表达。为了研究PRDM1α和PRDM1β表达可能的表观遗传改变,在B淋巴瘤细胞系和DLBCL样本中评估了这两种启动子异构体的甲基化情况。在淋巴瘤细胞中优先检测到PRDM1β CpG岛的低甲基化。然而,与非肿瘤病例的中度甲基化相比,在DLBCL病例中同时观察到PRDM1α CpG岛的高甲基化和低甲基化。在PRDM1β阳性的DLBCL样本中,CpG 16 - 21特异性高甲基化与PRDM1α的低表达相关。在DLBCL病例和非肿瘤反应性增生之间,有三种miRNA表达增加,一种miRNA表达减少,差异有统计学意义。因此,我们的结果表明,PRDM1α的异常甲基化沉默和PRDM1β的低甲基化激活在DLBCL中是常见事件。

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