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TET2 Promoter DNA Methylation and Expression Analysis in Pediatric B-cell Acute Lymphoblastic Leukemia

机译:小儿B细胞急性淋巴细胞白血病中TET2启动子DNA甲基化及表达分析

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摘要

TET2 is a novel tumor suppressor gene involved in several hematological malignancies of myeloid and lymphoid origin. Besides loss-of-function mutations and deletions, hypermethylation of the CpG island at the TET2 promoter was found in human cancer. Previous analysis revealed no TET2 mutations in acute lymphoblastic leukemia (ALL). Since the TET2 promoter methylation status in pediatric ALL has not been reported, the aim of the present study was to determine if promoter hypermethylation may be a mechanism of TET2 inactivation in a group of pediatric ALL cases. Methylation of TET2 promoter region in one (1/45) ALL B-common patient was detected by methylation specific polymerase chain reaction (PCR) and subsequently analyzed by bisulfite sequencing. We found no correlation between promoter methylation and gene expression, measured by quantitative reverse transcriptase-PCR, however the level of TET2 expression in ALL group was significantly decreased compared to children’s normal peripheral blood mononuclear cells and isolated B-cells. TET2 promoter hypermethylation seems to have limited clinical relevance in childhood B-cell ALL due to its low frequency.
机译:TET2是一种新型的肿瘤抑制基因,涉及髓样和淋巴样起源的几种血液系统恶性肿瘤。除了功能丧失的突变和缺失外,在人类癌症中还发现了TET2启动子上CpG岛的甲基化过高。先前的分析显示急性淋巴细胞白血病(ALL)中没有TET2突变。由于尚未报道儿科ALL中TET2启动子甲基化状态,因此本研究的目的是确定启动子高甲基化是否可能是一组儿科ALL病例中TET2失活的机制。通过甲基化特异性聚合酶链反应(PCR)检测一名(1/45)ALL B常见患者中TET2启动子区域的甲基化,随后通过亚硫酸氢盐测序进行分析。我们发现,通过定量逆转录酶PCR可以检测到启动子甲基化与基因表达之间没有相关性,但是与儿童正常的外周血单个核细胞和分离的B细胞相比,ALL组的TET2表达水平明显降低。 TET2启动子高甲基化由于其频率低,似乎在儿童B细胞ALL中的临床相关性有限。

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