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转录因子GATA-1与唐氏综合征白血病发生

Transcription factor GATA-1 and Down syndrome leukemogenesis.

作者信息

Muntean Andrew G, Ge Yubin, Taub Jeffrey W, Crispino John D

机构信息

Ben May Institute for Cancer Research, University of Chicago, IL 60637, USA.

出版信息

Leuk Lymphoma. 2006 Jun;47(6):986-97. doi: 10.1080/10428190500485810.

Abstract

Mutations in transcription factors constitute one means by which normal hematopoietic progenitors are converted to leukemic stem cells. Recently, acquired mutations in the megakaryocytic regulator GATA1 have been found in essentially all cases of acute megakaryoblastic leukemia (AMkL) in children with Down syndrome and in the closely related malignancy transient myeloproliferative disorder. In all cases, mutations in GATA1 lead to the expression of a shorter isoform of GATA-1, named GATA-1s. Because GATA-1s retains both DNA binding zinc fingers, but is missing the N-terminal transactivation domain, it has been predicted that the inability of GATA-1s to regulate its normal class of megakaryocytic target genes is the mechanism by which mutations in GATA1 contribute to the disease. Indeed, several recent reports have confirmed that GATA-1s fails to properly regulate the growth of megakaryocytic precursors, likely through aberrant transcriptional regulation. Although the specific target genes of GATA-1 mis-regulated by GATA-1s that drive this abnormal growth remain undefined, multiple candidate genes have been identified via gene array studies. Finally, the inability of GATA-1s to promote expression of important metabolic genes, such as cytadine deaminase, likely contributes to the remarkable hypersensitivity of AMkL blasts to cytosine arabinoside. Future studies to define the entire class of genes dysregulated by mutations in GATA1 will provide important insights into the etiology of these malignancies.

摘要

转录因子突变是正常造血祖细胞转化为白血病干细胞的一种方式。最近,在唐氏综合征患儿的几乎所有急性巨核细胞白血病(AMkL)病例以及密切相关的恶性肿瘤暂时性骨髓增殖性疾病中,均发现巨核细胞调节因子GATA1存在获得性突变。在所有病例中,GATA1突变导致一种较短的GATA-1异构体表达,名为GATA-1s。由于GATA-1s保留了两个DNA结合锌指,但缺少N端反式激活结构域,因此据推测,GATA-1s无法调节其正常的巨核细胞靶基因类别是GATA1突变导致疾病的机制。事实上,最近的几份报告证实,GATA-1s可能通过异常的转录调控无法正确调节巨核细胞前体的生长。尽管GATA-1s错误调节导致这种异常生长的GATA-1的特定靶基因仍未明确,但通过基因阵列研究已鉴定出多个候选基因。最后,GATA-1s无法促进重要代谢基因(如胞苷脱氨酶)的表达,可能导致AMkL原始细胞对阿糖胞苷具有显著的超敏感性。未来确定由GATA1突变失调的整个基因类别的研究将为这些恶性肿瘤的病因提供重要见解。

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