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Status |
Public on May 15, 2018 |
Title |
Selectively targeting bromodomain and extraterminal proteins for degradation as a novel anti-glioblastoma strategy [ChIP-seq] |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Purpose: Characterization of mechanism and vulnerability of BET protein dependency in GBM cells. Methods: ChIP-seq and RNA-seq were performed on GBM cells at different time points following treatment with dBET6, a novel BET protein degrader. The transcriptome responses of parental and JQ1-resistant U87 cells to JQ1 and dBET6 were compared as well. Result: This study reveals crucial functions of BET proteins and provides the rationale and therapeutic merits of targeted degradation of BET proteins by dBET6 in GBM.
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Overall design |
ChIP-seq of GBM cells following treatment with or without dBET6.
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Contributor(s) |
Xu L, Chen Y, Mayakonda A, Koeffler HP |
Citation(s) |
29764999 |
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Submission date |
May 22, 2017 |
Last update date |
Jul 25, 2021 |
Contact name |
Phillip H Koeffler |
E-mail(s) |
phillip_koeffler@nuhs.edu.sg
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Organization name |
Cancer Science Institute
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Lab |
H. Phillip Koeffler's lab
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Street address |
14 Medical Drive
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City |
Singapore |
ZIP/Postal code |
117599 |
Country |
Singapore |
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Platforms (1) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
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Samples (15)
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This SubSeries is part of SuperSeries: |
GSE99183 |
Selectively targeting bromodomain and extraterminal proteins for degradation as a novel anti-glioblastoma strategy NA-seq (time course) May 15, 2018 approved TSV |
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Relations |
BioProject |
PRJNA387463 |
SRA |
SRP107788 |