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急性淋巴细胞白血病的基因组学:见解与治疗意义。

Genomics in acute lymphoblastic leukaemia: insights and treatment implications.

机构信息

Department of Pathology, St Jude Children's Research Hospital, 262 Danny Thomas Place, Mail Stop 342, Memphis, TN 38105, USA.

出版信息

Nat Rev Clin Oncol. 2015 Jun;12(6):344-57. doi: 10.1038/nrclinonc.2015.38. Epub 2015 Mar 17.


DOI:10.1038/nrclinonc.2015.38
PMID:25781572
Abstract

Acute lymphoblastic leukaemia (ALL) is the commonest childhood cancer and an important cause of morbidity from haematological malignancies in adults. In the past several years, we have witnessed major advances in the understanding of the genetic basis of ALL. Genome-wide profiling studies, including microarray analysis and genome sequencing, have helped identify multiple key cellular pathways that are frequently mutated in ALL such as lymphoid development, tumour suppression, cytokine receptors, kinase and Ras signalling, and chromatin remodeling. These studies have characterized new subtypes of ALL, notably Philadelphia chromosome-like ALL, which is a high-risk subtype characterized by a diverse range of alterations that activate cytokine receptors or tyrosine kinases amenable to inhibition with approved tyrosine kinase inhibitors. Genomic profiling has also enabled the identification of inherited genetic variants of ALL that influence the risk of leukaemia development, and characterization of the relationship between genetic variants, clonal heterogeneity and the risk of relapse. Many of these findings are of direct clinical relevance and ongoing studies implementing clinical sequencing in leukaemia diagnosis and management have great potential to improve the outcome of patients with high-risk ALL.

摘要

急性淋巴细胞白血病(ALL)是最常见的儿童癌症,也是成年人血液系统恶性肿瘤发病率的重要原因。在过去的几年中,我们见证了对 ALL 遗传基础的理解的重大进展。全基因组分析研究,包括微阵列分析和基因组测序,有助于确定 ALL 中经常发生突变的多个关键细胞途径,如淋巴样发育、肿瘤抑制、细胞因子受体、激酶和 Ras 信号转导以及染色质重塑。这些研究描述了新的 ALL 亚型,特别是费城染色体样 ALL,这是一种高风险亚型,其特征是一系列不同的改变,这些改变激活细胞因子受体或酪氨酸激酶,可通过批准的酪氨酸激酶抑制剂抑制。基因组分析还能够确定影响白血病发生风险的 ALL 遗传变异,并描述遗传变异、克隆异质性与复发风险之间的关系。其中许多发现具有直接的临床相关性,正在进行的在白血病诊断和管理中实施临床测序的研究具有极大的潜力来改善高危 ALL 患者的预后。

相似文献

[1]
Genomics in acute lymphoblastic leukaemia: insights and treatment implications.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

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[2]
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[3]
Epigenomic insights and computational advances in hematologic malignancies.

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[4]
-rearranged acute lymphoblastic leukemia in infants: current progress and challenges.

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[5]
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[6]
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Biomedicines. 2024-11-29

[7]
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[8]
RanBALL: An Ensemble Random Projection Model for Identifying Subtypes of B-Cell Acute Lymphoblastic Leukemia.

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[9]
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[10]
Philadelphia chromosome-like acute lymphoblastic leukemia with concomitant rearrangements of CRLF2 and ABL1: a pediatric case report.

BMC Pediatr. 2024-8-10

本文引用的文献

[1]
Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia.

Nat Commun. 2015-3-19

[2]
The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.

Nat Genet. 2015-4

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Blood. 2014-12-2

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Science. 2014-11-13

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Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition.

Blood. 2014-11-27

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Regulation of transcription by long noncoding RNAs.

Annu Rev Genet. 2014

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N Engl J Med. 2014-9-11

[8]
A NOTCH1-driven MYC enhancer promotes T cell development, transformation and acute lymphoblastic leukemia.

Nat Med. 2014-10

[9]
Contrasting roles of histone 3 lysine 27 demethylases in acute lymphoblastic leukaemia.

Nature. 2014-10-23

[10]
Frequent cases of RAS-mutated Down syndrome acute lymphoblastic leukaemia lack JAK2 mutations.

Nat Commun. 2014-8-8

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