急性髓系白血病患者AML 1和P53肿瘤抑制基因表达的变化

F. Salarpour, K. Goudarzipour, A. Ahmadzadeh, M. Mohammadi, M. A. Farsani
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引用次数: 6

摘要

P53和aml1是调控造血过程中重要的抑癌基因,在维持造血增殖与分化的平衡中起着至关重要的作用。这些基因表达的改变可导致恶性肿瘤。本研究采用Real-Time-PCR技术对82例AML新生患者标本中P53和AML1基因与正常对照组的表达水平进行了比较。本研究结果显示,AML患者AML1基因表达水平明显高于正常对照组,P53基因表达水平明显低于正常对照组(P = 0.016和P = 0.002)。P53与AML1呈显著正相关(P= 0.037, r= 0.231)。P53的低水平表达是意料之中的,并且符合该基因作为肿瘤抑制基因的正常作用,然而AML1的过表达与其在髓细胞成熟中众所周知的作用相反。然而,该研究结果表明,尽管目前确定了该基因在髓细胞分化中的作用,但AML1的致癌形式(AML1a)可能已经增加,该异构体的高表达也可能作为其他正常AML1异构体和P53的抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes of AML 1 and P53 tumor suppressor gene expression in patients de novo acute myeloid leukemia
P53 and AML1are two important tumor suppressor genes in regulation of hematopoiesis with a critical role in keeping balance between proliferation and differentiation. Alternations in the expression of these genes can be resulted in malignancy. The present study investigated the expression levels of P53 and AML1 genes in 82 de novo AML patient specimens against normal control group using Real-Time-PCR. The results presented in this study revealed that AML1 gene expression was significantly higher and P53 gene expression levels was significantly lower in patients with AML in comparison with the normal control group (P = 0.016 and P = 0.002). Furthermore, the correlation between P53 and AML1 was significant and positive (P= 0.037 and r= 0.231). The lower levels of P53 expression were expected and in line with the normal role of this gene as a tumor suppressor gene, however AML1 over expression was in contrast with of its well-known role in myeloid maturation. However, This findings suggest that despite the current established role this genes in myeloid cell differentiation, oncogenic form of AML1 (AML1a) has possibly increased and high expression of this isoform may act as an inhibitor for other normal AML1 isoforms and P53 as well.
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