Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/129653
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Type: Journal article
Title: DUX hunting-clinical features and diagnostic challenges associated with DUX4-rearranged leukaemia
Author: Rehn, J.A.
O'Connor, M.J.
White, D.L.
Yeung, D.T.
Citation: Cancers, 2020; 12(10):1-15
Publisher: MDPI
Issue Date: 2020
ISSN: 2072-6694
2072-6694
Statement of
Responsibility: 
Jacqueline A. Rehn, Matthew J. O’Connor, Deborah L. White and David T. Yeung
Abstract: DUX4-rearrangement (DUX4r) is a recently discovered recurrent genomic lesion reported in 4-7% of childhood B cell acute lymphoblastic leukaemia (B-ALL) cases. This subtype has favourable outcomes, especially in children and adolescents treated with intensive chemotherapy. The fusion most commonly links the hypervariable IGH gene to DUX4 a gene located within the D4Z4 macrosatellite repeat on chromosome 4, with a homologous polymorphic repeat on chromosome 10. DUX4r is cryptic to most standard diagnostic techniques, and difficult to identify even with next generation sequencing assays. This review summarises the clinical features and molecular genetics of DUX4r B-ALL and proposes prospective new diagnostic methods.
Keywords: DUX4
ERG
acute lymphoblastic leukaemia
molecular subtype
Rights: © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
DOI: 10.3390/cancers12102815
Published version: http://dx.doi.org/10.3390/cancers12102815
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