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Status |
Public on Feb 24, 2021 |
Title |
Convergent organization of aberrant MYB complexes controls oncogenic gene expression in acute myeloid leukemia [RNAseq_MV411] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Dysregulated gene expression is one of the most prevalent features in human cancers. Here, we show that most subtypes of acute myeloid leukemia (AML) depend on the aberrant assembly of the MYB transcriptional co-activator complex. By rapid and selective peptidomimetic interference with the binding of CBP/P300 to MYB, but not CREB or MLL1, we find that the leukemic functions of MYB are mediated by CBP/P300-mediated co-activation of a distinct set of transcriptional factor complexes that are aberrantly assembled with MYB in AML cells. This therapeutic remodeling is accompanied by dynamic redistribution of CBP/P300 complexes to genes that control cellular differentiation and growth. Thus, aberrantly organized transcription factor complexes control convergent gene expression programs in AML cells. These findings establish a compelling strategy for pharmacologic reprogramming of oncogenic gene expression that supports its targeting for leukemias and other human cancers caused by dysregulated gene control.
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Overall design |
RNA-sequencing of a human leukemia cell line (MV411) treated with control PBS and peptidomimetic inhibitors over time
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Contributor(s) |
Forbes L, Takao S, Koche RP, Pineda JM, Bradley RK, Kentsis A |
Citation(s) |
33527899 |
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Submission date |
Dec 18, 2020 |
Last update date |
Feb 24, 2021 |
Contact name |
Richard Koche |
E-mail(s) |
kocher@mskcc.org
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Organization name |
Memorial Sloan Kettering Cancer Center
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Street address |
417 E. 68th St.
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City |
New York |
State/province |
New York |
ZIP/Postal code |
10065 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (18)
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This SubSeries is part of SuperSeries: |
GSE163470 |
Convergent organization of aberrant MYB complexes controls oncogenic gene expression in acute myeloid leukemia |
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Relations |
BioProject |
PRJNA686277 |
SRA |
SRP298437 |