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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 |
Appears in Collections: | Aurora harvest 8 Medicine publications |
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