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Items: 4

1.

An epigenetic vulnerability in PI3K/AKT inhibition resistant cancers is targetable by both bromodomain and HDAC inhibitors

(Submitter supplied) Acquisition of resistance to PI3K/AKT-targeted monotherapy regardless of cancer types implies the existence of common mechanisms. Here we demonstrate that while causing glycolysis crisis, acetyl-CoA shortage and global decrease of histone acetylation, PI3K/AKT inhibitors induce drug resistance by selectively augmenting CBP/p300, H3K27 acetylation and BRD4 binding at genomic loci of a subset of growth factor and receptor (GF/R) genes. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20301
32 Samples
Download data: BW
Series
Accession:
GSE147455
ID:
200147455
2.

Bromodomain and HDAC inhibitors equivalently suppress PI3K/AKT inhibition resistance in cancers

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21290 GPL20301
56 Samples
Download data: BW, XLS
Series
Accession:
GSE137209
ID:
200137209
3.

Illumina HiSeq 4000 (Homo sapiens)

Platform
Accession:
GPL20301
ID:
100020301
4.

PC3 GDC-resist p300 rep2

Organism:
Homo sapiens
Source name:
prostate
Platform:
GPL20301
Series:
GSE137209 GSE147455
Download data: BW
Sample
Accession:
GSM4431269
ID:
304431269
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Supplemental Content

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