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Status |
Public on Apr 17, 2014 |
Title |
Hes6 expression is controlled by c-Myc and the AR to promote E2F1 activity and poor outcome in castrate-resistant prostate cancer (cMyc ChIP-seq) |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Hes6 is a transcription co-factor that is associated with stem cell characteristics in neural tissue, but its role in cancer remains uncertain. Here we show that Hes6 is controlled by c-Myc and the AR and can drive castration resistance in xenografts of the androgen-dependent LNCaP prostate cancer cell line model. Hes6 activates a cell cycle enhancing transcriptional network that maintains tumour growth in the absence of circulating androgen but with maintained nuclear AR. We demonstrate interaction between E2F1, the AR and Hes6 and show the co-dependency of these factors in the castration-resistant setting. In the clinical setting, we have discovered a Hes6-associated signature that predicts poor outcome in prostate cancer, which could be pharmacologically targeted.
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Overall design |
Myc ChIPseq on LNCaP cells.
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Contributor(s) |
Lamb AD, Ramos-Montoya A, Russell R |
Citation(s) |
24737870 |
Submission date |
Apr 26, 2012 |
Last update date |
Feb 21, 2019 |
Contact name |
Roslin Russell |
E-mail(s) |
roslin.russell@cruk.cam.ac.uk
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Phone |
01223 769770
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Organization name |
Cambridge Research Institute, Cancer Research UK
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Street address |
Robinson Way
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City |
Cambridge |
ZIP/Postal code |
CB2 0RE |
Country |
United Kingdom |
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Platforms (1) |
GPL9052 |
Illumina Genome Analyzer (Homo sapiens) |
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Samples (3) |
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This SubSeries is part of SuperSeries: |
GSE36526 |
Hes6 drives a network with therapeutic potential in castrate-resistant prostate cancer |
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Relations |
BioProject |
PRJNA162291 |