Pre-B acute lymphoblastic leukaemia recurrent fusion, EP300-ZNF384, is associated with a distinct gene expression

被引:29
|
作者
McClure, Barbara J. [1 ,2 ]
Heatley, Susan L. [1 ,2 ]
Kok, Chung H. [1 ,2 ]
Sadras, Teresa [1 ,2 ]
An, Jiyuan [1 ]
Hughes, Timothy P. [1 ,2 ,3 ]
Lock, Richard B. [4 ,5 ]
Yeung, David [1 ,2 ,3 ]
Sutton, Rosemary [4 ,5 ,6 ]
White, Deborah L. [1 ,2 ,6 ,7 ]
机构
[1] SAHMRI, Canc Theme, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Sch Med, Adelaide, SA 5000, Australia
[3] SA Pathol, Haematol Dept, Adelaide, SA 5000, Australia
[4] Univ New South Wales, Lowy Canc Res Ctr, Childrens Canc Inst, Sydney, NSW 2000, Australia
[5] Univ New South Wales, Sch Womens & Childrens Hlth, Sydney, NSW 2000, Australia
[6] Murdoch Childrens Res Inst, AGHA, Parkville, Vic 3052, Australia
[7] Univ Adelaide, Sch Paediat, Adelaide, SA 5000, Australia
基金
英国医学研究理事会;
关键词
REARRANGEMENTS; MODULATION; FREQUENCY; P300;
D O I
10.1038/s41416-018-0022-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Zinc-finger protein 384 (ZNF384) fusions are an emerging subtype of precursor B-cell acute lymphoblastic leukaemia (pre-B-ALL) and here we further characterised their prevalence, survival outcomes and transcriptome. METHODS: Bone marrow mononuclear cells from 274 BCR-ABL1-negative pre-B-ALL patients were immunophenotyped and transcriptome molecularly characterised. Transcriptomic data was analysed by principal component analysis and gene-set enrichment analysis to identify gene and pathway expression changes. RESULTS: We exclusively detect E1A-associated protein p300 (EP300)-ZNF384 in 5.7% of BCR-ABL1-negative adolescent/young adult (AYA)/adult pre-B-ALL patients. EP300-ZNF384 patients do not appear to be a high-risk subgroup. Transcriptomic analysis revealed that EP300-ZNF384 samples have a distinct gene expression profile that results in the up-regulation of Janus kinase/signal transducers and activators of transcription (JAK/STAT) and cell adhesion pathways and down-regulation of cell cycle and DNA repair pathways. CONCLUSIONS: Importantly, this report contributes to a better overview of the incidence of EP300-ZNF384 patients and show that they have a distinct gene signature with concurrent up-regulation of JAK-STAT pathway, reduced expression of B-cell regulators and reduced DNA repair capacity.
引用
收藏
页码:1000 / 1004
页数:5
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