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Links from GEO DataSets

Items: 20

1.
Full record GDS3864

In vivo glucocorticoid effect on non-leukemic peripheral blood lymphocytes

Analysis of mononuclear cells from non-leukemic individuals (1 healthy/3 epileptic) up to 24 hr after glucocorticoid (GC) injection. GCs induce apoptosis and are used to treat lymphoid malignancies. Results provide insight into molecular mechanisms responsible for the anti-leukemic GC effects.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 2 disease state, 4 individual, 4 time sets
Platform:
GPL570
Series:
GSE22779
16 Samples
Download data: CEL
2.

Gene expression data of non-leukemic individuals before and during in-vivo glucocorticoid treatment

(Submitter supplied) Article title: Expression, regulation and function of phosphofructo-kinase/fructose-biphosphatases (PFKFBs) in glucocorticoid-induced apoptosis of acute lymphoblastic leukemia cells. Glucocorticoids (GCs) cause apoptosis and cell cycle arrest in lymphoid cells and constitute a central component in the therapy of lymphoid malignancies, most notably childhood acute lymphoblastic leukemia (ALL). PFKFB2 (6-phosphofructo-2-kinase/fructose-2,6-biphosphatase-2), a kinase controlling glucose metabolism, was identified by us previously as a GC response gene in expression profiling analyses performed in children with ALL during initial systemic GC mono-therapy. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3864
Platform:
GPL570
16 Samples
Download data: CEL
Series
Accession:
GSE22779
ID:
200022779
3.

Gene expression data of glucocorticoid resistant and sensitive acute lymphoblastic leukemia cell lines

(Submitter supplied) Gene expression data of glucocorticoid resistant and sensitive acute lymphoblastic leukemia cell lines for the article: Expression, regulation and function of phosphofructo-kinase/fructose-biphosphatases (PFKFBs) in glucocorticoid-induced apoptosis of acute lymphoblastic leukemia cells Glucocorticoids (GCs) cause apoptosis and cell cycle arrest in lymphoid cells and constitute a central component in the therapy of lymphoid malignancies, most notably childhood acute lymphoblastic leukemia (ALL). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4203
Platform:
GPL570
24 Samples
Download data: CEL
Series
Accession:
GSE22152
ID:
200022152
4.
Full record GDS4203

Dexamethasone effect on glucocorticoid-resistant and -sensitive lymphoblastic leukemia cell lines

Analysis of glucocorticoid (GC)-resistant and -sensitive derivatives of the CEM-C7H2 T-ALL cell line following 6hrs of dexamethasone treatment. GC drugs are a central component of childhood ALL therapy. Results provide insight into molecular mechanisms underlying the anti-leukemic effects of GC.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 2 cell line sets
Platform:
GPL570
Series:
GSE22152
24 Samples
Download data: CEL
5.

thymic mouse cells

(Submitter supplied) Glucocorticoids (GC) are in most chemotherapy protocols for lymphoid malignancies, particularly childhood acute lymphoblastic leukaemia (ALL) for their ability to induce apoptosis in malignant blast. The underlying mechanism, however, has so far only been investigated in model systems. This study comprises Affymetrix hgu133 plus 2.0 analyses of Peripheral blood lymphoblasts purified at three time points (0h, 6-8h, 24h after treatment initiation) from 13 children under therapy for ALL . more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
5 Samples
Download data: CEL, XLS
Series
Accession:
GSE2843
ID:
200002843
6.

Additional systems to Prednisolone treated childhood ALL samples

(Submitter supplied) Glucocorticoids (GC) are in most chemotherapy protocols for lymphoid malignancies, particularly childhood acute lymphoblastic leukaemia (ALL) for their ability to induce apoptosis in malignant blast. The underlying mechanism, however, has so far only been investigated in model systems. This study comprises Affymetrix hgu133 plus 2.0 analyses of Peripheral blood lymphoblasts purified at three time points (0h, 6-8h, 24h after treatment initiation) from 13 children under therapy for ALL . more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
45 Samples
Download data: CEL, XLS
Series
Accession:
GSE2842
ID:
200002842
7.

Prednisolone treated childhood ALL samples

(Submitter supplied) Glucocorticoids (GC) are in most chemotherapy protocols for lymphoid malignancies, particularly childhood acute lymphoblastic leukaemia (ALL) for their ability to induce apoptosis in malignant blast. The underlying mechanism, however, has so far only been investigated in model systems. This study comprises Affymetrix hgu133 plus 2.0 analyses of Peripheral blood lymphoblasts purified at three time points (0h, 6-8h, 24h after treatment initiation) from 13 children under therapy for ALL . more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
39 Samples
Download data: CEL, XLS
Series
Accession:
GSE2677
ID:
200002677
8.

ZBTB16, a glucocorticoid response gene in acute lymphoblastic leukemia, interferes with glucocorticoid-induced apoptosis

(Submitter supplied) Glucocorticoids (GCs) cause apoptosis in lymphoid lineage cells and are therefore widely used in the therapy of lymphoid malignancies. The molecular mechanisms of the anti-leukemic GC effects are, however, poorly understood. We have previously defined a list of GC-regulated candidate genes by Affymetrix-based whole genome comparative expression profiling in children with acute lymphoblastic leukemia (ALL) during systemic GC monotherapy and in experimental systems of GC-induced apoptosis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8476
40 Samples
Download data: CEL
Series
Accession:
GSE15820
ID:
200015820
9.

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:
GPL13490 GPL13454
66 Samples
Download data: CEL
Series
Accession:
GSE29063
ID:
200029063
10.

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
11.

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
12.

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
13.

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
14.

CCRF-CEM Prednisolone treatment at 4h and 72h

(Submitter supplied) It has been shown previously that glucocorticoids exert a dual mechanism of action, entailing cytotoxic, mitogenic as well as cell proliferative and anti-apoptotic responses, in a dose-dependent manner on CCRF-CEM cells at 72 h. Early gene expression response implies a dose-dependent dual mechanism of action of prednisolone too, something reflected on cell state upon 72 h of treatment. In this work, a generic, computational microarray data analysis framework is proposed, in order to examine the hypothesis whether CCRF-CEM cells exhibit an intrinsic or acquired mechanism of resistance and to investigate the molecular imprint of this, upon prednisolone treatment. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL13250 GPL13251
11 Samples
Download data: TXT
Series
Accession:
GSE28154
ID:
200028154
15.

CCRF-CEM Prednisolone treatment at 4h

(Submitter supplied) Background: Glucocorticoids are important pharmaceutical agents in the treatment of acute lymphoblastic leukemia in children. Resistance or sensitivity to glucocorticoids is considered to be of crucial importance for disease prognosis. Prednisolone is a first-line chemotherapeutic agent in the treatment of acute lymphoblastic leukemia. Here, the effects of prednisolone on the resistant CCRF-CEM leukemic cell line were studied. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13250
9 Samples
Download data: TXT
Series
Accession:
GSE27989
ID:
200027989
16.

Glucocorticoid-regulated microRNAs and mirtrons in acute lymphoblastic leukemia

(Submitter supplied) Glucocorticoids (GC) have a major impact on the biology of normal and malignant cells of the lymphoid lineage. This includes induction of apoptosis which is exploited in the therapy of acute lymphoblastic leukemia (ALL) and related lymphoid malignancies. MicroRNAs (miRNAs) and the related mirtrons are ~22 nucleotide RNA molecules implicated in the control of essential biological functions including proliferation, differentiation and apoptosis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE11336
ID:
200011336
17.

Glucocorticoid-regulated microRNAs and mirtrons in human acute lymphoblastic leukemia

(Submitter supplied) Glucocorticoids (GC) have a major impact on the biology of normal and malignant cells of the lymphoid lineage. This includes induction of apoptosis which is exploited in the therapy of acute lymphoblastic leukemia (ALL) and related lymphoid malignancies. MicroRNAs (miRNAs), and the related mirtrons, are ~22 nucleotide RNA molecules implicated in the control of essential biological functions including proliferation, differentiation and apoptosis. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platforms:
GPL6608 GPL6609
48 Samples
Download data: CEL
Series
Accession:
GSE10910
ID:
200010910
18.

The synthetic glucocorticoids prednisolone and dexamethasone regulate the same genes in acute lymphoblastic leukemia cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18412
21 Samples
Download data: CEL
Series
Accession:
GSE55878
ID:
200055878
19.

The synthetic glucocorticoids prednisolone and dexamethasone regulate the same genes in acute lymphoblastic leukemia cells [Set 2]

(Submitter supplied) Background: Glucocorticoids (GCs) cause apoptosis in malignant cells of lymphoid lineage by transcriptionally regulating a plethora of genes. As a result, GCs are included in almost all treatment protocols for lymphoid malignancies, particularly childhood acute lymphoblastic leukemia (chALL). The most commonly used synthetic GCs in the clinical setting are prednisolone and dexamethasone. While the latter has a higher activity and more effectively reduces the tumor load in patients, it is also accompanied by more serious adverse effects than the former. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18412
9 Samples
Download data: CEL
Series
Accession:
GSE55877
ID:
200055877
20.

The synthetic glucocorticoids prednisolone and dexamethasone regulate the same genes in acute lymphoblastic leukemia cells

(Submitter supplied) Background: Glucocorticoids (GCs) cause apoptosis in malignant cells of lymphoid lineage by transcriptionally regulating a plethora of genes. As a result, GCs are included in almost all treatment protocols for lymphoid malignancies, particularly childhood acute lymphoblastic leukemia (chALL). The most commonly used synthetic GCs in the clinical setting are prednisolone and dexamethasone. While the latter has a higher activity and more effectively reduces the tumor load in patients, it is also accompanied by more serious adverse effects than the former. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL18412
12 Samples
Download data: CEL
Series
Accession:
GSE55876
ID:
200055876
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