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Links from GEO DataSets

Items: 20

1.

Expression microarray screen for genes regulated by the unliganded glucocorticoid receptor

(Submitter supplied) To further characterize the role of the unliganded glucocorticoid receptor (GR) in breast cells, we used an shRNA vector directed against GR to create EPH-4 mouse mammary cell lines with depleted endogenous levels of this receptor. RNA prepared from normal (EV-50) and GR-depleted (shGR-19) cells was used in an expression microarray screen for targets of unliganded GR. This analysis revealed 260 targets of negaive regulation by unliganded GR, and 343 targets of positive regulation by unliganded GR, several of which were involved in pro-apoptotic networks, and opposed the activity of liganded GR targets. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
4 Samples
Download data: TXT
Series
Accession:
GSE51408
ID:
200051408
2.

Gene Regulation by the Human Glucocorticoid Receptor Dimerization Domain Mutant dim4

(Submitter supplied) A mutation in the dimerization domain of the mouse glucocorticoid receptor (GR), dim1, has recently been shown to bind DNA and regulate gene expression. To expand these studies we created a stable osteosarcoma (U-2 OS) cell line expressing four mutations in the dimerization domain of the human GR, dim4 (N454D, A458T, R460D, D462C), and used whole human genome microarray analysis to compare differences in gene regulation between vehicle treated (CON) and those treated with the glucocorticoid receptor agonist dexamethasone (DEX) at 100nM concentration for 6 hours.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
6 Samples
Download data: TXT
Series
Accession:
GSE26857
ID:
200026857
3.

Time course of glucocortiocid receptor isoforms

(Submitter supplied) Glucocorticoids regulate diverse physiologic processes and synthetic derivatives of these natural hormones are widely used in the treatment of inflammatory diseases. However, chronic administration often triggers insensitivity and serious side effects including osteoporosis. The underlying mechanisms regulating these side effects are not completely understood. We report here that human osteosarcoma U-2 OS bone cells lacking the glucocorticoid receptor (GR) are resistant to glucocorticoid killing whereas the expression of wild-type GR activates an apoptotic program. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3432
Platform:
GPL1708
60 Samples
Download data: TIFF, TXT
Series
Accession:
GSE6711
ID:
200006711
4.
Full record GDS3432

Osteosarcoma cell line response to activation of specific glucocorticoid receptor alpha isoforms: time course

Analysis of glucocorticoid receptor alpha (hGRalpha) isoform -A, -B, -C, or -D expressing osteosarcoma cells for up to 24 h after hGRalpha activation with dexomethasone. Cell apoptosis occurred in a GR isoform-selective manner. Results provide insight into the function of each isoform.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 5 agent, 4 time sets
Platform:
GPL1708
Series:
GSE6711
60 Samples
Download data: TIFF, TXT
5.

Time course microarray data following GR activation in MCF10A-Myc breast cells

(Submitter supplied) This series contain time course microarray data from MCF10A-Myc cells treated with either ethanol or Dexamethasone for 30 min, 2 hr, 4 hr, and 24 hr. This series contains three biological replicates that were analyzed as independent replicate experiments (data were normalized within each replicate experiment, not across all samples). Keywords: time course
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS2095 GDS2096 GDS2097
Platform:
GPL96
24 Samples
Download data: CEL
Series
Accession:
GSE4917
ID:
200004917
6.
Full record GDS2097

Glucocorticoid receptor activation effect on breast cancer cells: time course (series 3)

Analysis of breast cancer MCF10A-Myc cells at various time points up to 24 hours following treatment with dexamethasone to activate the glucocorticoid receptor (GR). GR activation is critical in the stress response of virtually all cell types.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 4 time sets
Platform:
GPL96
Series:
GSE4917
8 Samples
Download data: CEL
DataSet
Accession:
GDS2097
ID:
2097
7.
Full record GDS2096

Glucocorticoid receptor activation effect on breast cancer cells: time course (series 2)

Analysis of breast cancer MCF10A-Myc cells at various time points up to 24 hours following treatment with dexamethasone to activate the glucocorticoid receptor (GR). GR activation is critical in the stress response of virtually all cell types.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 4 time sets
Platform:
GPL96
Series:
GSE4917
8 Samples
Download data: CEL
DataSet
Accession:
GDS2096
ID:
2096
8.
Full record GDS2095

Glucocorticoid receptor activation effect on breast cancer cells: time course (series 1)

Analysis of breast cancer MCF10A-Myc cells at various time points up to 24 hours following treatment with dexamethasone to activate the glucocorticoid receptor (GR). GR activation is critical in the stress response of virtually all cell types.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 4 time sets
Platform:
GPL96
Series:
GSE4917
8 Samples
Download data: CEL
DataSet
Accession:
GDS2095
ID:
2095
9.

Comparison of glucocorticoid receptor (NR3C1) binding in wild type and Klf15-/- MEFs

(Submitter supplied) The objective of this study was to dertemine GR binding patterns within wild type murine embryonic fibroblasts in comparison to embryonic fibroblasts derived from mice containing a null mutation for Klf15.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
7 Samples
Download data: BED
Series
Accession:
GSE69947
ID:
200069947
10.

Specificity quantification of Glucocorticoid receptor binding using high-throughput sequencing

(Submitter supplied) In this work, we used our recently developed method Spec-seq to characterize the binding specificity of Glucocorticoid receptor in vitro.
Organism:
Homo sapiens
Type:
Other
Platform:
GPL15520
2 Samples
Download data: TXT
Series
Accession:
GSE69386
ID:
200069386
11.

GR and Klf15 regulate gene expression dynamics and integrate signals through feed forward circuitry

(Submitter supplied) The glucocorticoid receptor (GR) regulates adaptive transcriptional programs that alter metabolism in response to stress. Network properties that allow GR to tune gene expression to match specific physiologic demands are poorly understood. We analyzed the transcriptional consequences of GR activation in murine lungs deficient for Klf15, a transcriptional regulator of amino acid metabolism that is induced by glucocorticoids and fasting
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
29 Samples
Download data: TXT
Series
Accession:
GSE44695
ID:
200044695
12.

GR and ER co-activation alters the expression of differentiation genes and associates with improved ER+ breast cancer outcome

(Submitter supplied) Analysis of MCF-7 cells treated for 4h with Ethanol, Estradiol (E2), Dexamethasone (Dex), or Estradiol + Dexamethasone (E2 + Dex) In estrogen receptor (ER)-negative breast cancer (BC), high tumor glucocorticoid receptor (GR) expression has been associated with a relatively poor outcome. In contrast, using a meta-analysis of several genomic datasets, here we find that tumor GR mRNA expression is associated with improved ER+ relapse-free survival (RFS) (independently of progesterone receptor (PR) expression). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE79761
ID:
200079761
13.

Whole-genome GR binding sites and histone acetylation status in pediatric acute lymphoblastic leukemia patient-derived xenografts following dexamethasone treatment in vivo

(Submitter supplied) Glucocorticoids are critical components of combination chemotherapy regimens in pediatric acute lymphoblastic leukemia (ALL). However, the signaling pathways regulating apoptosis in glucocorticoid-treated lymphoid cells remain unclear. In this study, pediatric ALL patient-derived xenograft inherently sensitive to glucocorticoids were exposed to dexamethasone in vivo. Whole-genome GR binding sites and histone acetylation status were detected using chromatin immunoprecipitation sequencing analyses. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: BED, BW
Series
Accession:
GSE58266
ID:
200058266
14.

in vivo dexamethasone-induced gene expression in pediatric acute lymphoblastic leukemia patient-derived xenografts

(Submitter supplied) Glucocorticoids are critical components of combination chemotherapy regimens in pediatric acute lymphoblastic leukemia (ALL). The pro-apoptotic BIM protein is an important mediator of glucocorticoid-induced apoptosis in normal and malignant lymphocytes, while the anti-apoptotic BCL2 confers resistance. The signaling pathways regulating BIM and BCL2 expression in glucocorticoid-treated lymphoid cells remain unclear. more...
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6884
58 Samples
Download data: TXT
Series
Accession:
GSE57795
ID:
200057795
15.

The Glucocorticoid Receptor Interferes with Progesterone Receptor-Dependent Genomic Regulation in Breast Cancer Cells

(Submitter supplied) The glucocorticoid and progesterone receptors (GR and PR) are closely related members of the steroid receptor family. Despite sharing similar structural and functional characteristics; the cognate hormones display very distinct physiological responses. In mammary epithelial cells, PR activation is associated with the incidence and progression of breast cancer, whereas the GR is related to growth suppression and differentiation. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9052
8 Samples
Download data: BED
Series
Accession:
GSE126859
ID:
200126859
16.

Distinct genome-wide, gene-specific selectivity patterns of four glucocorticoid receptor coregulators

(Submitter supplied) Glucocorticoids are a class of steroid hormones that bind to and activate the Glucocorticoid Receptor, which then positively or negatively regulates transcription of many genes that govern multiple important physiological pathways such as inflammation and metabolism of glucose, fat and bone. Previous studies focusing on single coregulators demonstrated that each coregulator is required for regulation of only a subset of all the genes regulated by a steroid hormone. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
40 Samples
Download data: TXT
Series
Accession:
GSE58715
ID:
200058715
17.

Analysis of glucocorticoid receptor (NR3C1), NFkb (p65 subunit), and RNA polymerase 2 (RNAP2) binding in Beas-2B airway epithelial cells

(Submitter supplied) The objective of this study was to determine binding patterns for GR, 65 and RNAP2 in Beas-2B airway epithelial cells after treatment with dexamethasone (100 nm), TNF (20 ng/ml) or both for one hour.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
21 Samples
Download data: BED
Series
Accession:
GSE79803
ID:
200079803
18.

Selective enhancement and repression of glucocorticoid receptor signaling by coregulator Hic-5

(Submitter supplied) The glucocorticoid receptor (GR) recruits many coregulators via the well characterized AF2 interaction surface in the GR ligand binding domain, but LIM domain coregulator Hic-5 binds to the relatively uncharacterized tau2 activation domain in the hinge region of GR. Requirement of Hic-5 for glucocorticoid-regulated gene expression in U2OS osteosarcoma cells was defined by Hic-5 depletion and global gene expression analysis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5269
Platform:
GPL10558
48 Samples
Download data: TXT
Series
Accession:
GSE46448
ID:
200046448
19.
Full record GDS5269

Hydrogen peroxide-inducible clone-5 deficiency effect on dexamethasone-treated osteosarcoma cells: time course

Analysis of U2OS-GR osteosarcoma cells (which stably express glucocorticoid receptor α) depleted for hydrogen peroxide-inducible clone-5 (Hic-5) then treated with the GR ligand dexamethasone for up to 24hrs. Results provide insight into the role of LIM domain coregulator Hic-5 in GR signaling.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 3 protocol, 4 time sets
Platform:
GPL10558
Series:
GSE46448
48 Samples
Download data
20.

Expression data from dexamethasone treated mouse embryonic neural progenitor/stem cells isolated from wild type C57Bl/6 or caveolin-1 knockout mice

(Submitter supplied) Neurosphere cultures prepared from E14.5 mouse cerebral cortex at passage 3 were treated for 4 hours with 100 nM dexamethasone We used microarrays to detail the global program of dexamethasone regulated gene expression in embryonic neural progenitor/stem cells
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5256
Platform:
GPL8321
20 Samples
Download data: CEL
Series
Accession:
GSE49804
ID:
200049804
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