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Status |
Public on Oct 21, 2014 |
Title |
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies [expression array] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
The polycomb repressive complex 2 (PRC2) exerts oncogenic effects in many tumour types1. However, loss-of-function mutations in PRC2 components occur in a subset of haematopoietic malignancies, sug- gesting that this complex plays a dichotomous and poorly understood role in cancer2,3. Here we provide genomic, cellular, and mouse mod- elling data demonstrating that the polycomb group gene SUZ12 func- tions as tumour suppressor in PNS tumours, high-grade gliomas and melanomas by cooperating with mutations in NF1. NF1 encodes a Ras GTPase-activating protein (RasGAP) and its loss drives cancer by activating Ras4. We show that SUZ12 loss potentiates the effects of NF1 mutations by amplifying Ras-driven transcription through effects on chromatin. Importantly, however, SUZ12 inactivation also triggers an epigenetic switch that sensitizes these cancers to bromodomain inhib- itors. Collectively, these studies not only reveal an unexpected con- nection between the PRC2 complex, NF1 and Ras, but also identify a promising epigenetic-based therapeutic strategy that may be exploited for a variety of cancers.
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Overall design |
9 samples in triplicates, 3x LacZ control, 3x SUZ12 over expression, 3x JQ1 treatment
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Contributor(s) |
De Raedt T, Cichowski K |
Citation(s) |
25119042 |
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Submission date |
Oct 20, 2014 |
Last update date |
Jul 26, 2018 |
Contact name |
Thomas De Raedt |
E-mail(s) |
tderaedt@rics.bwh.harvard.edu
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Organization name |
Harvard Medical School - Brigham Women's Hospital
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Department |
Medicine
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Lab |
Cichowski Lab
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Street address |
77 Avenue Louis Pasteur
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
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Platforms (1) |
GPL6244 |
[HuGene-1_0-st] Affymetrix Human Gene 1.0 ST Array [transcript (gene) version] |
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Samples (9)
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This SubSeries is part of SuperSeries: |
GSE52777 |
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies |
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Relations |
BioProject |
PRJNA264622 |