Abstract
To define the mutation spectrum in non-Down syndrome acute megakaryoblastic leukemia (non-DS-AMKL), we performed transcriptome sequencing on diagnostic blasts from 14 pediatric patients and validated our findings in a recurrency/validation cohort consisting of 34 pediatric and 28 adult AMKL samples. Our analysis identified a cryptic chromosome 16 inversion (inv(16)(p13.3q24.3)) in 27% of pediatric cases, which encodes a CBFA2T3-GLIS2 fusion protein. Expression of CBFA2T3-GLIS2 in Drosophila and murine hematopoietic cells induced bone morphogenic protein (BMP) signaling and resulted in a marked increase in the self-renewal capacity of hematopoietic progenitors. These data suggest that expression of CBFA2T3-GLIS2 directly contributes to leukemogenesis.
Copyright © 2012 Elsevier Inc. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Bone Morphogenetic Proteins / metabolism
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Child
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Chromosome Inversion
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Chromosomes, Human, Pair 16
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Drosophila / genetics
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Drosophila / growth & development
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Gene Expression Profiling
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Humans
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Kruppel-Like Transcription Factors / genetics*
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Leukemia, Megakaryoblastic, Acute / classification
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Leukemia, Megakaryoblastic, Acute / diagnosis
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Leukemia, Megakaryoblastic, Acute / genetics*
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Mice
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Oncogene Proteins, Fusion / genetics*
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Oncogene Proteins, Fusion / metabolism
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Oncogene Proteins, Fusion / physiology
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Prognosis
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Recombinant Fusion Proteins / genetics
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Recombinant Fusion Proteins / metabolism
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Recombinant Fusion Proteins / physiology
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Repressor Proteins / genetics*
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Sequence Analysis, RNA
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Signal Transduction
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Tumor Suppressor Proteins / genetics*
Substances
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Bone Morphogenetic Proteins
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CBFA2T3 protein, human
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CBFA2T3-GLIS2 fusion protein, human
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GLIS2 protein, human
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Kruppel-Like Transcription Factors
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Oncogene Proteins, Fusion
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Recombinant Fusion Proteins
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Repressor Proteins
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Tumor Suppressor Proteins