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P15INK4b基因甲基化与骨髓增生异常综合征

P15INK4b gene methylation and myelodysplastic syndromes.

作者信息

Quesnel B, Fenaux P

机构信息

INSERM U524, IRCL, Lille, France.

出版信息

Leuk Lymphoma. 1999 Nov;35(5-6):437-43. doi: 10.1080/10428199909169608.

Abstract

Myelodysplastic syndromes (MDS) are clonal disorders, which frequently undergo leukemic transformation. It was recently shown that the promoter of the p15INK4b but not the p16INK4a gene is frequently and selectively hypermethylated in MDS. The p15INK4b gene is a cyclin dependent kinase inhibitor gene, which is actively transcribed after TGFbeta exposure. Methylation of the p15INK4b gene is significantly correlated with blastic bone marrow involvement, and sequential analyses have shown that methylation increases with disease evolution toward AML. These data strongly suggest that p15INK4b gene methylation is a mechanism allowing leukemic cells to escape to inhibitory signals from the bone marrow environment, however the exact role of p15INK4b gene methylation in disruption of the signal mediated by TGFbeta remains to be investigated.

摘要

骨髓增生异常综合征(MDS)是克隆性疾病,常发生白血病转化。最近研究表明,p15INK4b基因而非p16INK4a基因的启动子在MDS中经常且选择性地发生高甲基化。p15INK4b基因是一种细胞周期蛋白依赖性激酶抑制基因,在暴露于转化生长因子β(TGFβ)后会被激活转录。p15INK4b基因的甲基化与骨髓原始细胞浸润显著相关,连续分析表明,随着疾病向急性髓系白血病(AML)进展,甲基化程度增加。这些数据强烈提示,p15INK4b基因甲基化是白血病细胞逃避骨髓环境抑制信号的一种机制,然而p15INK4b基因甲基化在破坏TGFβ介导信号中的具体作用仍有待研究。

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