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小儿急性巨核细胞白血病:多功能融合蛋白与致癌协同作用

Pediatric Acute Megakaryoblastic Leukemia: Multitasking Fusion Proteins and Oncogenic Cooperations.

作者信息

Lopez Cécile K, Malinge Sébastien, Gaudry Muriel, Bernard Olivier A, Mercher Thomas

机构信息

INSERM U1170, Equipe Labellisée Ligue Contre le Cancer, 94800 Villejuif, France; Gustave Roussy, 94800 Villejuif, France; Université Paris-Sud, 91405 Orsay, France.

INSERM U1170, Equipe Labellisée Ligue Contre le Cancer, 94800 Villejuif, France; Gustave Roussy, 94800 Villejuif, France; Université Paris Diderot, 75013 Paris, France.

出版信息

Trends Cancer. 2017 Sep;3(9):631-642. doi: 10.1016/j.trecan.2017.07.003. Epub 2017 Aug 18.

Abstract

Pediatric leukemia presents specific clinical and genetic features from adult leukemia but the underpinning mechanisms of transformation are still unclear. Acute megakaryoblastic leukemia (AMKL) is the malignant accumulation of progenitors of the megakaryocyte lineage that normally produce blood platelets. AMKL is diagnosed de novo, in patients showing a poor prognosis, or in Down syndrome (DS) patients with a better prognosis. Recent data show that de novo AMKL is primarily associated with chromosomal alterations leading to the expression of fusions between transcriptional regulators. This review highlights the most recurrent genetic events found in de novo pediatric AMKL patients and, based on recent functional analyses, proposes a mechanism of leukemogenesis common to de novo and DS-AMKL.

摘要

小儿白血病呈现出与成人白血病不同的特定临床和遗传特征,但其转化的潜在机制仍不清楚。急性巨核细胞白血病(AMKL)是正常情况下产生血小板的巨核细胞系祖细胞的恶性积累。AMKL可在预后不良的患者中初发诊断,或在预后较好的唐氏综合征(DS)患者中诊断。最近的数据表明,初发AMKL主要与导致转录调节因子之间融合表达的染色体改变有关。本综述重点介绍了初发小儿AMKL患者中最常见的遗传事件,并基于最近的功能分析,提出了一种初发和DS-AMKL共有的白血病发生机制。

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