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Links from GEO DataSets

Items: 7

1.

Transcriptome profile of breast cancer HS-578T cells overexpressing EP300

(Submitter supplied) HS-578T cells overexpressing EP300 show an increase in doxorubicin and paclitaxel resistance, up-regulation of EMT markers together with an increase in motility and invasion, and an increase in the percentage of cancer stem cells and mammosphere formation.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL23159
6 Samples
Download data: CEL
Series
Accession:
GSE116370
ID:
200116370
2.

Gene Expression Pattern in EP300 knocked-down MCF7 cells and corresponding paclitaxel resistant derivatives

(Submitter supplied) EP300, a transcriptional co-activator of E-cadherin, has been recently found by our group to regulate doxorubicin resistance via by-pass of senescence and paclitaxel resistance by overcoming apoptosis in a minimally transformed mammary epithelial cells (MTMEC). Moreover, EP300 deleted MTMEC cells exhibit an multi-drug resistant (MDR) phenotype independent of P-glycoprotein (ABCB1), an efflux pump or ABC drug transporter. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
16 Samples
Download data: CEL
Series
Accession:
GSE76200
ID:
200076200
3.

Next generation sequencing analysis of control and KSR1 knockdown CRC cell line translatomes.

(Submitter supplied) KSR1 signaling alters the translational landscape of human CRC cells to support their survival. To determine the effect of KSR1 on translatomes in colon cancer cells, we performed genome-wide polysome profiling. We stably expressed short hairpin RNA (shRNA) constructs targeting KSR1 or a non-targeting control in two K-Ras mutant CRC cell lines, HCT116 and HCT15. We isolated and quantified both total mRNA and efficiently translated mRNAs (associated with ≥ 3 ribosomes) using RNA sequencing. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21697
24 Samples
Download data: TXT
4.

Expression data from knockdown of G9a in MDA-MB231 cells

(Submitter supplied) G9a is an H3K9m2 methyltransferase, which is critical in controlling gene suppression and DNA methylation. We used microarray analysis to identify the target genes that are regulated by G9a in MDA-MB231 cells, in which E-cadherin is silenced.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4800
Platform:
GPL6244
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE34925
ID:
200034925
5.
Full record GDS4800

H3K9me2 methyltransferase G9a depletion effect on breast cancer cell line

Analysis of MDA-MB231 breast cancer cells depleted for G9a, a methyltransferase that mediates histone H3 lysine-9 di-methylation (H3K9me2). G9a depletion inhibits migratory ability and invasiveness of MDA-MB231 cells. Results provide insight into role of G9a and H3K9me2 in breast cancer progression.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6244
Series:
GSE34925
6 Samples
Download data: CEL, CHP
6.

CREBBP/EP300 bromodomain inhibition affects the proliferation of AR positive breast cancer cell lines

(Submitter supplied) Changes in gene expression caused by CREBBP/EP300 bromodomain inhibitors in breast cancer cell lines
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
18 Samples
Download data: TXT
Series
Accession:
GSE114937
ID:
200114937
7.

Group 3 medulloblastomatranscriptional networks collapse under domain-specific EP300/CBP inhibition.

(Submitter supplied) EP300 and CBP are paralogous, multidomain histone acetyltransferases (HATs) that regulate gene expression by binding to and acetylating diverse proteins. With widespread effects on gene regulation, these enzymes are attractive targets for therapeutic development. Discovery efforts for chemical inhibitors typically target protein domains that are amenable to probe binding. In some cases, probes have been identified for more than one domain within a single protein, including high potency inhibitors of both the catalytic HAT domain and bromodomain (BRD) that mediate the enzymatic and protein binding (“reader”) activities of EP300/CBP. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
24 Samples
Download data: TXT
Series
Accession:
GSE233609
ID:
200233609
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Supplemental Content

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