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唐氏综合征和急性巨核细胞白血病患者中的GATA1突变并不总是预示着良好的预后。

GATA1 mutations in patients with down syndrome and acute megakaryoblastic leukaemia do not always confer a good prognosis.

作者信息

Ariffin Hany, Garcia Jaime Castillo, Daud Siti Sarah, Ibrahim Kamariah, Aizah Nik, Ong Gek-Bee, Chong Lee-Ai, Mohamad Zulqarnain

机构信息

Department of Paediatrics, University of Malaya Medical Centre, Kuala Lumpur, Malaysia.

出版信息

Pediatr Blood Cancer. 2009 Jul;53(1):108-11. doi: 10.1002/pbc.21983.

Abstract

Children with Down syndrome and acute megakaryoblastic leukemia (DS-AMKL) have been shown to have increased sensitivity to cytarabine based chemotherapy. The excellent prognosis in patients with DS-AMKL may be due to mutations in the GATA1 gene leading to reduced expression of the enzyme cytidine deaminase. This leads to a decreased ability to convert cytarabine into its inactive metabolite, resulting in high intracellular concentration of this cytotoxic agent. We report two cases of DS-AMKL with GATA1 mutations who had poor outcome. These patients had high expression levels of cytidine deaminase mRNA transcripts. We speculate that other factors can affect overall outcome in patients with DS-AMKL irrespective of the presence of GATA1 mutations.

摘要

患有唐氏综合征和急性巨核细胞白血病(DS-AMKL)的儿童已被证明对基于阿糖胞苷的化疗更为敏感。DS-AMKL患者预后良好可能是由于GATA1基因突变导致胞苷脱氨酶表达降低。这导致将阿糖胞苷转化为其无活性代谢物的能力下降,从而使这种细胞毒性药物在细胞内浓度升高。我们报告了两例患有GATA1突变的DS-AMKL病例,其预后较差。这些患者的胞苷脱氨酶mRNA转录物表达水平较高。我们推测,无论是否存在GATA1突变,其他因素均可影响DS-AMKL患者的总体预后。

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