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伴 X;6 号染色体长臂 11 区带;23 号染色体长臂 1 区带易位的急性髓系白血病;MYB-GATA1 和女性性别:GATA1 不足可能不足以引起发病机制。

Acute myeloid leukemia with t(X;6)9p11;q23);MYB-GATA1 and female sex: GATA1 insufficiency may be insufficient for pathogenesis.

机构信息

Division of Laboratory Medicine, Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, 4650 Sunset Blvd., Mailstop #32, Los Angeles, CA 90027, United States.

Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russian Federation.

出版信息

Cancer Genet. 2022 Jan;260-261:37-40. doi: 10.1016/j.cancergen.2021.11.007. Epub 2021 Dec 5.

Abstract

Pediatric acute myeloid leukemia (AML) is genetically heterogenous (Olsson et al., 2016). t(X;6)(p11;q23) is a rare but recurrent chromosomal translocation in infant AML thought to be associated with male sex and basophilic differentiation (Dastugue et al., 1997). Here we report molecular characterization of AML with t(X;6)(p11;q23);MYB-GATA1 in two female infants and demonstrate preserved GATA1 expression in the sample tested. These findings further debunk a concept that this fusion was restricted to males, in whom it disrupts the only copy of the X-linked GATA1 gene, causing presumable complete loss of GATA1 function. Our data also demonstrate the power and efficiency of RNA sequencing for subclassification of leukemia on a clinically relevant timeline.

摘要

儿科急性髓细胞白血病(AML)在遗传上具有异质性(Olsson 等人,2016 年)。t(X;6)(p11;q23) 是婴儿 AML 中一种罕见但反复出现的染色体易位,据信与男性和嗜碱性分化有关(Dastugue 等人,1997 年)。在这里,我们报告了两例患有 t(X;6)(p11;q23);MYB-GATA1 的 AML 的分子特征,并证明了在测试的样本中 GATA1 表达得到了保留。这些发现进一步推翻了一个概念,即这种融合仅限于男性,在男性中,它会破坏唯一的 X 连锁 GATA1 基因,导致 GATA1 功能的推定完全丧失。我们的数据还表明,RNA 测序在临床上相关的时间范围内对白血病进行亚分类具有强大的效率。

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