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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

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

作者信息

Musialik Ewa, Bujko Mateusz, Wypych Agnieszka, Matysiak Michał, Siedlecki Janusz Aleksander

机构信息

Department of Molecular and Translational Oncology, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology , Warsaw, Poland.

Department of Pediatric Haematology and Oncology, Medical University of Warsaw , Poland.

出版信息

Hematol Rep. 2014 Mar 28;6(1):5333. doi: 10.4081/hr.2014.5333. eCollection 2014 Jan 29.

Abstract

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.

摘要

TET2是一种新型肿瘤抑制基因,与多种髓系和淋巴系起源的血液系统恶性肿瘤有关。除功能丧失性突变和缺失外,在人类癌症中还发现TET2启动子处的CpG岛发生高甲基化。先前的分析显示急性淋巴细胞白血病(ALL)中不存在TET2突变。由于尚未报道小儿ALL中TET2启动子甲基化状态,本研究的目的是确定启动子高甲基化是否可能是一组小儿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)检测了1例(1/45)B系普通ALL患者中TET2启动子区域的甲基化情况,随后通过亚硫酸氢盐测序进行分析。我们发现启动子甲基化与通过定量逆转录PCR测量的基因表达之间没有相关性,然而与儿童正常外周血单个核细胞和分离的B细胞相比,ALL组中TET2的表达水平显著降低。由于TET2启动子高甲基化频率较低,其在儿童B细胞ALL中的临床相关性似乎有限。

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