共 50 条
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
相关论文