Molecular pathogenesis of AML: Translating insights to the clinic Journal Article


Author: Levine, R. L.
Article Title: Molecular pathogenesis of AML: Translating insights to the clinic
Abstract: Specific combinations of mutations, including FLT3 and IDH1/IDH2/TET2, frequently co-occur in acute myeloid leukemia (AML) and are associated with poor prognosis. These mutation combinations can be modeled in mice to provide a more genetically accurate model of AML. Within these models, stem cells may be different depending on how experiments are conducted and based on context. No one mutation can turn on a gene; rather the perfect storm of the right genes in the right cell is necessary to produce AML. Furthermore, this understanding is therapeutically relevant. Rapid and accurate targeted DNA sequencing will identify mutations of prognostic and therapeutic significance and will guide treatment choices in the future. © 2013 Elsevier Ltd. All rights reserved.
Keywords: acute granulocytic leukemia; gene mutation; gene sequence; overall survival; pathogenesis; nonhuman; allele; gene; gene expression profiling; cytogenetics; stem cell; dna sequence; tet2 gene; leukemia remission; aml; asxl1 gene; tet2; idh1 gene; idh2 gene; acute myeloid leukemia; flt3; gemtuzumab; cancer prognosis; dnmt3a gene; flt3 gene; dna sequencing; human; priority journal; article; murine models
Journal Title: Best Practice and Research: Clinical Haematology
Volume: 26
Issue: 3
ISSN: 1521-6926
Publisher: Elsevier Inc.  
Date Published: 2013-09-01
Start Page: 245
End Page: 248
Language: English
DOI: 10.1016/j.beha.2013.10.003
PROVIDER: scopus
PMCID: PMC3869618
PUBMED: 24309525
DOI/URL:
Notes: Export Date: 2 January 2014 -- CODEN: BPRCA -- Source: Scopus
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  1. Ross Levine
    778 Levine