Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/128601
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Type: Journal article
Title: MLLT10 rearranged acute leukemia: incidence, prognosis and possible therapeutic strategies
Author: Forgione, M.O.
McClure, B.J.
Yeung, D.T.
Eadie, L.N.
White, D.L.
Citation: Genes Chromosomes and Cancer, 2020; 59(12):709-721
Publisher: Wiley
Issue Date: 2020
ISSN: 1045-2257
1098-2264
Statement of
Responsibility: 
Michelle O. Forgione, Barbara J. McClure, David T. Yeung, Laura N. Eadie, Deborah L. White
Abstract: Rearrangements of the MLLT10 gene occur in acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL), most commonly T-lineage ALL (T-ALL), in patients of all ages. MLLT10 rearranged (MLLT10r) acute leukemia presents a complex diagnostic and therapeutic challenge due to frequent presentation of immature or mixed phenotype, and a lack of consensus regarding optimal therapy. Cases of MLLT10r AML or T-ALL bearing immature phenotype are at high risk of poor outcome, but the underlying molecular mechanisms and sensitivity to targeted therapies remain poorly characterized. This review addresses the incidence and prognostic significance of MLLT10r in acute leukemia, and how the aberrant gene expression profile of this disease can inform potential targeted therapeutic strategies. Understanding the underlying genomics of MLLT10r acute leukemia, both clinically and molecularly, will improve prognostic stratification and accelerate the development of targeted therapeutic strategies, to improve patient outcomes.
Keywords: AF10; leukemia genomics; MLLT10; MLLT10 rearrangements; t(10;11)(p12‐13;q14‐21)
Rights: © 2020 Wiley Periodicals LLC
DOI: 10.1002/gcc.22887
Grant ID: NHMRC
Published version: http://dx.doi.org/10.1002/gcc.22887
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