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回溯儿童白血病的发病根源:一场加法的较量。

Backtracking childhood leukaemia to birth: A battle of addition.

机构信息

Division of Epidemiology and Clinical Research, Department of Pediatrics, University of Minnesota Medical School, Minneapolis, Minnesota, USA.

Center for Genetic Epidemiology, Department of Population and Public Health Sciences, University of Southern California Keck School of Medicine, USC Norris Comprehensive Cancer Center, Los Angeles, California, USA.

出版信息

Br J Haematol. 2024 Nov;205(5):1670-1671. doi: 10.1111/bjh.19747. Epub 2024 Sep 5.

DOI:10.1111/bjh.19747
PMID:39238151
Abstract

Paediatric leukaemia has a long tail of driver mutations each of which must be 'backtracked' to samples taken at birth to identify the prenatal origin of a subtype. Presently, Bardini et al. describe the first successful backtracking of an NUTM1 rearrangement, which sheds light on the biology of this particular alteration. Continued backtracking of NUTM1 rearrangements, and all leukaemia-typical somatic alterations, is necessary to fully understand the prenatal origin of these diseases. Commentary on: Bardini et al. Prenatal origin of NUTM1 gene rearrangement in infant B-cell precursor acute lymphoblastic leukaemia. Br J Haematol 2024; 205:1883-1888.

摘要

儿科白血病有一系列长的驱动突变,每一个都必须“回溯”到出生时采集的样本,以确定亚型的产前起源。目前,Bardini 等人描述了首例成功回溯 NUTM1 重排,这揭示了这种特殊改变的生物学特征。继续回溯 NUTM1 重排以及所有白血病典型的体细胞改变,对于全面了解这些疾病的产前起源是必要的。述评:Bardini 等人。婴儿 B 细胞前体急性淋巴细胞白血病中 NUTM1 基因重排的产前起源。英国血液学杂志 2024;205:1883-1888。

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Prenatal origin of NUTM1 gene rearrangement in infant B-cell precursor acute lymphoblastic leukaemia.婴儿 B 细胞前体急性淋巴细胞白血病中 NUTM1 基因重排的产前起源。
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本文引用的文献

1
Backtracking NOM1::ETV6 fusion to neonatal pathogenesis of t(7;12) (q36;p13) infant AML.追溯NOM1::ETV6融合与t(7;12)(q36;p13)婴儿急性髓系白血病新生儿发病机制的关系。
Leukemia. 2024 Aug;38(8):1808-1812. doi: 10.1038/s41375-024-02293-9. Epub 2024 May 28.
2
In Utero Origins of Acute Leukemia in Children.儿童急性白血病的子宫内起源
Biomedicines. 2024 Jan 19;12(1):236. doi: 10.3390/biomedicines12010236.
3
Backtracking to the future: unraveling the origins of childhood leukemia.回溯未来:揭开儿童白血病的起源之谜
Leukemia. 2024 Feb;38(2):416-419. doi: 10.1038/s41375-023-02111-8. Epub 2023 Dec 20.
4
Covert pre-leukaemic clones in healthy co-twins of patients with childhood acute lymphoblastic leukaemia.儿童急性淋巴细胞白血病患者健康双胞胎中的隐匿性白血病前期克隆
Leukemia. 2023 Jan;37(1):47-52. doi: 10.1038/s41375-022-01756-1. Epub 2022 Dec 20.
5
Favorable outcome of NUTM1-rearranged infant and pediatric B cell precursor acute lymphoblastic leukemia in a collaborative international study.一项国际合作研究中NUTM1重排的婴幼儿及儿童B细胞前体急性淋巴细胞白血病的良好预后
Leukemia. 2021 Oct;35(10):2978-2982. doi: 10.1038/s41375-021-01333-y. Epub 2021 Jul 1.
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Toward prevention of childhood ALL by early-life immune training.通过生命早期的免疫训练预防儿童 ALL。
Blood. 2021 Oct 21;138(16):1412-1428. doi: 10.1182/blood.2020009895.
7
The Prenatal Origin of Childhood Leukemia: Potential Applications for Epidemiology and Newborn Screening.儿童白血病的产前起源:在流行病学和新生儿筛查中的潜在应用
Front Pediatr. 2021 Apr 23;9:639479. doi: 10.3389/fped.2021.639479. eCollection 2021.
8
Droplet Digital PCR Improves IG-/TR-based MRD Risk Definition in Childhood B-cell Precursor Acute Lymphoblastic Leukemia.液滴数字PCR改善了儿童B细胞前体急性淋巴细胞白血病中基于IG/TR的微小残留病风险定义。
Hemasphere. 2021 Feb 24;5(3):e543. doi: 10.1097/HS9.0000000000000543. eCollection 2021 Mar.
9
is a recurrent fusion gene partner in B-cell precursor acute lymphoblastic leukemia associated with increased expression of genes on chromosome band 10p12.31-12.2.是B细胞前体急性淋巴细胞白血病中一种反复出现的融合基因伙伴,与染色体带10p12.31 - 12.2上基因的表达增加相关。
Haematologica. 2019 Oct;104(10):e455-e459. doi: 10.3324/haematol.2018.206961. Epub 2019 Mar 14.
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