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Links from GEO DataSets

Items: 20

1.

Individual-specific functional epigenomics reveals genetic determinants of adverse metabolic effects of glucocorticoids

(Submitter supplied) Glucocorticoids (GCs) are widely used as anti-inflammatory drugs, but their long-term use has severe metabolic side effects. Here, by treating multiple patient-derived adipose stem cell-derived adipocytes and iPSC-derived hepatocytes with the potent GC dexamethasone (Dex), we uncovered cell type-specific and individual-specific GC-dependent transcriptomes and glucocorticoid receptor (GR) cistromes. Patient-specific GR binding could be traced to single nucleotide polymorphisms (SNPs) that altered the binding motifs of GR or its cooperating factors. We also discovered another set of genetic variants that modulated Dex response through affecting chromatin accessibility or chromatin architecture. Several SNPs that altered Dex-regulated GR binding and gene expression controlled Dex-driven metabolic perturbations and, remarkably, predicted metabolic side-effects of GC-treated patients. These data validate a patient stem cell-based experimental framework to discover genetic variants that impact GR function and individual responses to GC drugs, with implications for developing personalized therapies.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
4 related Platforms
177 Samples
Download data: BIGWIG, HIC, TXT
2.

mRNA profiling of human Multipotent Adipose-Derived Stem (hMADS) cells transfected with miR-29a and subjected to adipocyte differentiation

(Submitter supplied) The human microRNA hsa-miR-29a is a member of the miR-29 family of microRNAs, which is expressed in the adipogenic lineage. To identify putative direct target mRNAs of the miR-29 family, and to get an idea about potential functions of the miR-29 family in adipocyte development, we transfected human Multipotent Adipose-Derived Stem (hMADS) cells with miR-29a mimics (leading to elevation of intracellular levels of mature miR-29a). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL19627
7 Samples
Download data: GPR
Series
Accession:
GSE65704
ID:
200065704
3.

HAND2 is a novel obesity-linked adipogenic transcription factor regulated by glucocorticoid signaling

(Submitter supplied) Aims: Adipocytes are critical cornerstones of energy metabolism. While obesity-induced adipocyte dysfunction is associated with insulin resistance and systemic metabolic disturbances, adipogenesis, the formation of new adipocytes and healthy adipose tissue expansion are associated with metabolic benefits. Understanding the molecular mechanisms governing adipogenesis is of great clinical potential to efficiently restore metabolic health in obesity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL23159
9 Samples
Download data: CEL
Series
Accession:
GSE148699
ID:
200148699
4.

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
5.
Full record GDS5256

Caveolin-1 deficiency effect on dexamethasone treatment: embryonic day E14.5 cerebral cortex

Analysis of E14.5 cerebral cortex, Caveolin-1 (Cav-1) deficient, cultured neurospheres treated with glucocorticoid (GC) dexamethasone (100nM, 4h). Cav-1 involved in GC signaling in neural stem cells. Results provide insight into role of Cav-1 in GC treatment and impact fetal brain development.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 2 genotype/variation sets
Platform:
GPL8321
Series:
GSE49804
20 Samples
Download data: CEL
6.

Anti-inflammatory Chromatinscape Associated with Clinically Relevant Timing of Glucocorticoid Treatment

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
30 Samples
Download data: BEDGRAPH, CSV, FPKM_TRACKING
Series
Accession:
GSE93739
ID:
200093739
7.

Anti-inflammatory Chromatinscape Associated with Clinically Relevant Timing of Glucocorticoid Treatment [DNase-seq]

(Submitter supplied) Despite the widespread use of glucocorticoids (GCs) for treating inflammatory conditions, the underlying mechanisms of their anti-inflammatory effects are not understood. Moreover, the majority of molecular investigations have examined the effects of glucocorticoid receptor (GR) activation prior to inflammatory challenges. However, clinically relevant situations are emulated by a GC intervention initiated in the midst of rampant inflammatory responses. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: BEDGRAPH, CSV
Series
Accession:
GSE93738
ID:
200093738
8.

Anti-inflammatory Chromatinscape Associated with Clinically Relevant Timing of Glucocorticoid Treatment [ChIP-seq]

(Submitter supplied) Despite the widespread use of glucocorticoids (GCs) for treating inflammatory conditions, the underlying mechanisms of their anti-inflammatory effects are not understood. Moreover, the majority of molecular investigations have examined the effects of glucocorticoid receptor (GR) activation prior to inflammatory challenges. However, clinically relevant situations are emulated by a GC intervention initiated in the midst of rampant inflammatory responses. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
10 Samples
Download data: BEDGRAPH, CSV
Series
Accession:
GSE93736
ID:
200093736
9.

Anti-inflammatory Chromatinscape Associated with Clinically Relevant Timing of Glucocorticoid Treatment [RNA-Seq]

(Submitter supplied) Despite the widespread use of glucocorticoids (GCs) for treating inflammatory conditions, the underlying mechanisms of their anti-inflammatory effects are not understood. Moreover, the majority of molecular investigations have examined the effects of glucocorticoid receptor (GR) activation prior to inflammatory challenges. However, clinically relevant situations are emulated by a GC intervention initiated in the midst of rampant inflammatory responses. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
14 Samples
Download data: FPKM_TRACKING
Series
Accession:
GSE93735
ID:
200093735
10.

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
11.

Expression data from the stomach of mice treated with dexamethasone.

(Submitter supplied) Glucocorticoids are used for the treatment of inflammatory conditions but they also cause many side-effects. We used microarrays to detail the changes in gene expression induced in the stomach upon oral glucocorticoid treatment.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL15733
6 Samples
Download data: CEL
Series
Accession:
GSE51669
ID:
200051669
12.

Postnatal glucocorticoids suppress myelination in a dose-dependent manner by genomic mechanism

(Submitter supplied) Objective: Postnatal glucocorticoids (GCs) are widely used in the prevention of chronic lung disease in premature infants. However, their use is associated with neurodevelopmental delay and cerebral palsy. We hypothesized that postnatal dexamethasone or betamethasone in high-dose, but not low-dose, would induce hypomyelination, astrogliosis, and motor impairment in premature rabbit pups. Additionally, these effects would be mediated by glucocorticoid receptors (GRs). more...
Organism:
Oryctolagus cuniculus
Type:
Expression profiling by array
Platform:
GPL7083
8 Samples
Download data: TXT
Series
Accession:
GSE44610
ID:
200044610
13.

Differential effect of glucocorticoids on the activation of monocytes and macrophages.

(Submitter supplied) Glucocorticoids (GCs) reduce the expression of many genes induced in inflammatory conditions in vivo or by pro-inflammatory stimuli in vitro acting on the Glucocorticoid receptor (GR/NR3C1). However, GCs have pleiotropic effects on the immune system. Monocytes and macrophages are important cells of the innate immune system, exhibiting complex properties with enhancing as well as suppressive effects on inflammatory processes depending on their stage of activation and differentiation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL26999
11 Samples
Download data: RCC
Series
Accession:
GSE135165
ID:
200135165
14.

Differential effect of glucocorticoids on the activation of monocytes and macrophages

(Submitter supplied) The Glucocorticoid receptor (GR/NR3C1) is expressed in almost all immune cells. Glucocorticoids (GCs) are potent regulators of inflammation with effects mainly immunosuppressive. While, GCs have pleiotropic effects on Macrophages exhibiting complex properties with enhancing as well as suppressive effects on inflammatory processes depending on their stage of differentiation and activation, the mechanisms of GCs actions on Monocytes and Macrophages and their contribution to systemic anti-inflammatory effects remain unclear. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
12 Samples
Download data: TXT
Series
Accession:
GSE135130
ID:
200135130
15.

Transcriptional glucocorticoid-response at the exon level and NR3C1 DNA-binding in childhood leukemia models: mRNA and ChIP-chip profiling

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL13454 GPL13490
66 Samples
Download data: CEL
Series
Accession:
GSE29063
ID:
200029063
16.

Transcriptional glucocorticoid-response at the exon level and NR3C1 DNA-binding in childhood leukemia models; NR3C1-DNA binding in NALM6 precursor B-ALL cells.

(Submitter supplied) Glucorticoids (GCs) are steroid hormones with a wide range of physiological actions in different cell types and tissues. Their ability to induce apoptosis in malignant cells of the lymphoid lineage is exploited since decades in the treatment of childhood acute lymphoblastic leukemia (ALL), the molecular mechanism of this cell death induction being however still unknown. Using an integrative approach we delineated the transcriptional response of a preB- and a T-ALL model system employing Exon microarrays and identified in vivo interactions of the transcription factor GC receptor (GR) with genes' promoters in the same samples using the ChIP-on-chip technology. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL13490
12 Samples
Download data: CEL
Series
Accession:
GSE29057
ID:
200029057
17.

Transcriptional glucocorticoid-response at the exon level and NR3C1 DNA-binding in childhood leukemia models; NR3C1-DNA binding in CCRF-CEM-C7H2 T-ALL cells.

(Submitter supplied) Glucorticoids (GCs) are steroid hormones with a wide range of physiological actions in different cell types and tissues. Their ability to induce apoptosis in malignant cells of the lymphoid lineage is exploited since decades in the treatment of childhood acute lymphoblastic leukemia (ALL), the molecular mechanism of this cell death induction being however still unknown. Using an integrative approach we delineated the transcriptional response of a preB- and a T-ALL model system employing Exon microarrays and identified in vivo interactions of the transcription factor GC receptor (GR) with genes' promoters in the same samples using the ChIP-on-chip technology. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL13490
12 Samples
Download data: CEL
Series
Accession:
GSE29056
ID:
200029056
18.

Transcriptional glucocorticoid-response at the exon level and NR3C1 DNA-binding in childhood leukemia models; transcriptional response in NALM6 precursor B-ALL cells.

(Submitter supplied) Glucorticoids (GCs) are steroid hormones with a wide range of physiological actions in different cell types and tissues. Their ability to induce apoptosis in malignant cells of the lymphoid lineage is exploited since decades in the treatment of childhood acute lymphoblastic leukemia (ALL), the molecular mechanism of this cell death induction being however still unknown. Using an integrative approach we delineated the transcriptional response of a preB- and a T-ALL model system employing Exon microarrays and identified in vivo interactions of the transcription factor GC receptor (GR) with genes' promoters in the same samples using the ChIP-on-chip technology. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13454
18 Samples
Download data: CEL
Series
Accession:
GSE29049
ID:
200029049
19.

Transcriptional glucocorticoid-response at the exon level and NR3C1 DNA-binding in childhood leukemia models; transcriptional response in CCRF-CEM-C7H2 T-ALL cells.

(Submitter supplied) Glucorticoids (GCs) are steroid hormones with a wide range of physiological actions in different cell types and tissues. Their ability to induce apoptosis in malignant cells of the lymphoid lineage is exploited since decades in the treatment of childhood acute lymphoblastic leukemia (ALL), the molecular mechanism of this cell death induction being however still unknown. Using an integrative approach we delineated the transcriptional response of a preB- and a T-ALL model system employing Exon microarrays and identified in vivo interactions of the transcription factor GC receptor (GR) with genes' promoters in the same samples using the ChIP-on-chip technology. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13454
24 Samples
Download data: CEL
Series
Accession:
GSE29003
ID:
200029003
20.

Glucocoritcoid regulated genes in omental and subcutaneous human adipose tissues

(Submitter supplied) To provide a comprehensive understanding of how GC affect adipose tissue and adipocyte function, we analyzed patterns of gene expression after culture of abdominal subcutaneous (sc) and omental (Om)) Adipose tissue of severely obese subjects (3F, 1M) in the presence of insulin or insulin (7 nM) plus dexamethasone (dex, 25 nM) for 7d.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL8300 GPL91
14 Samples
Download data: CEL, TXT
Series
Accession:
GSE26123
ID:
200026123
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