Common and overlapping oncogenic pathways contribute to the evolution of acute myeloid leukemias.
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ABSTRACT: In this report we demonstrate that the ability to alter self-renewal in vitro and in vivo is a more generalized property of leukemia-associated oncogenes. We further demonstrate that disparate leukemia-associated oncogenes initiate early common and overlapping transformation and self-renewal gene expression programs to mediate these effects. Furthermore, elements of these programs can be detected in established leukemia stem cells from an animal model and across a large cohort of patients with differing acute myeloid leukemia (AML) subtypes, where they strongly predict for disease biology. Finally, individual genes from the programs are demonstrated to partially phenocopy the leukemia-associated oncogenes and themselves alter self-renewal in committed murine progenitors and generate AML when expressed in murine bone marrow.
ORGANISM(S): Homo sapiens
PROVIDER: GSE23143 | GEO | 2011/06/27
SECONDARY ACCESSION(S): PRJNA131699
REPOSITORIES: GEO
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