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MDM2 SNP309 启动子多态性是慢性淋巴细胞白血病的一个独立预后因素。

MDM2 SNP309 promoter polymorphism, an independent prognostic factor in chronic lymphocytic leukemia.

机构信息

Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.

出版信息

Eur J Haematol. 2010 Sep;85(3):251-6. doi: 10.1111/j.1600-0609.2010.01470.x. Epub 2010 May 14.

Abstract

BACKGROUND

The single nucleotide polymorphism SNP309 with a change from T to G in the promoter region of the MDM2 gene is shown to increase the MDM2 protein levels and attenuate the p53 levels and associates with disease progression in several tumors.

OBJECTIVE

In this study, the role of the polymorphism was investigated with regard to the clinical outcome in B-cell chronic lymphocytic leukemia (B-CLL).

PATIENTS

A total of 210 patients with B-CLL were followed for up to 19 yr.

RESULTS

The overall survival (OS) of patients with at least one G-allele was significantly shorter when compared with those with two T-alleles (P = 0.024) with a more pronounced difference in patients below the median age. Age at onset of B-CLL was similar irrespective of MDM2 status. The presence of a G-allele in combination with TP53 mutations or unmutated IgVH gene status resulted in an additive risk of death.

CONCLUSION

In this report, with a high proportion of B-CLL patients with an advanced Binet stage and with an unmutated IgVH gene, MDM2 SNP309 was found to be independently associated with OS. The survival difference was more pronounced in younger patients.

摘要

背景

MDM2 基因启动子区域的单核苷酸多态性 SNP309 由 T 突变为 G,可增加 MDM2 蛋白水平,降低 p53 水平,并与几种肿瘤的疾病进展相关。

目的

本研究旨在探讨该多态性与 B 细胞慢性淋巴细胞白血病(B-CLL)患者临床结局的关系。

患者

共 210 例 B-CLL 患者随访时间长达 19 年。

结果

与携带两个 T 等位基因的患者相比,至少携带一个 G 等位基因的患者总生存期(OS)明显缩短(P = 0.024),且在中位年龄以下的患者中差异更为显著。发病时年龄与 MDM2 状态无关。G 等位基因与 TP53 突变或未突变的 IgVH 基因状态并存会增加死亡风险。

结论

本报告中,在 Binet 分期较高且 IgVH 基因未突变的 B-CLL 患者中,MDM2 SNP309 与 OS 独立相关。年轻患者的生存差异更为显著。

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