急性白血病Tp53基因P1启动子区DNA甲基化异常

Yongxin Zheng, F. Guo, Y. Zou, Wu Jun
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摘要

本研究旨在探讨急性白血病患者p53基因P1启动子区DNA甲基化异常。应用聚合酶链式反应(PCR)检测31例新诊断白血病患者新鲜白血病细胞及单核细胞白血病U937细胞中Tp53基因的异常DNA甲基化。结果显示,在31例白血病患者(38.7%)和U937细胞中检测到Tp53 P1启动子区DNA甲基化异常,而在正常对照组(11例健康志愿者)中未检测到该基因的DNA甲基化异常,说明急性白血病患者与健康供者之间存在显著差异(P=0.0183, Fisher精确检验)。急性髓性白血病(AML)和急性淋巴性白血病(ALL)患者的外周血淋巴细胞密度差异无统计学意义(35.2% vs 42.8%, P=0.7241, Fisher精确检验)。我们的研究结果为我们所知的第一次提供了实验室证据,证明Tp53基因P1启动子区DNA甲基化异常在AML和ALL患者中都是一种普遍现象,这种特殊的DNA甲基化在急性白血病中的意义需要进一步深入研究。
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Aberrant DNA Methylation in P1 Promoter Region of Tp53 Gene in Acute Leukemia
The present study was undertaken to investigate the aberrant DNA ethymlation in P1 promoter region of p53 gene in acute leukemia patients. The aberrant DNA methylation of Tp53 gene in fresh leukemia cells obtained from 31 newly diagnosed patients as well as monocyte leukemia U937 cells were detected by using polymerase chain reaction (PCR). The results revealed that aberrant DNA methylation in P1 promoter region of Tp53 was detectable in 12 cases of 31 leukemia patients (38.7%) as well as in U937 cells, while no aberrant DNA methylation of this gene was detected in normal control group (11 healthy volunteers), indicating that there was significant difference between acute leukemia patients and healthy donors (P=0.0183, Fisher’s exact test). Furthermore, no significant difference was found in acute myeloid leukemia (AML) and acute lymphoid leukemia (ALL) patients (35.2% vs 42.8%, P=0.7241, Fisher’s exact test). Our results, for the first time to our knowledge, provide laboratory evidence that aberrant DNA methylation in P1 promoter region of Tp53 gene is an common phenomenon in both AML and ALL patients, and that the significance of this special DNA methylation in acute leukemia needs further and profound investigation.
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