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Links from GEO DataSets

Items: 17

1.
Full record GDS5637

Platelet-derived growth factor inhibitor effect on lymphocytic cells expressing FIP1L1-PDGFRα or ETV6-PDGFRβ

Analysis of Ba/F3 cells expressing a constitutively active form of PDGFRα or PDGFRβ oncogene (Fip1L1-PDGFRα or TEL-PDGFRβ) and treated with imatinib (Glivec), a potent PDGFR inhibitor. Results provide insight into target genes of the PI3K/PKB/FOXO pathway downstream of growth factor stimulation.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 agent, 3 genotype/variation, 2 growth protocol sets
Platform:
GPL8321
Series:
GSE44810
6 Samples
Download data: CEL, CHP, DAT, XML
DataSet
Accession:
GDS5637
ID:
5637
2.

Ba/F3 cells expressing ETV6-PDGFRb and FIP1L1-PDGFRa treated or not with Glivec

(Submitter supplied) Gene expression profiles in Ba/F3 cells expressing ETV6-PDGFRB, FIP1L1-PDGFRA or a control vector, treated or not with imatinib (Glivec)
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS5637
Platform:
GPL8321
6 Samples
Download data: CEL, CHP, DAT, XML
Series
Accession:
GSE44810
ID:
200044810
3.

Human fibroblast stimulation with PDGF-BB or b-FGF

(Submitter supplied) We analyzed gene expression in human fibroblasts stimulated by platelet-derived growth factor-BB (PDGF-BB) or basic fibroblast growth factor (bFGF) for 1h and 24h. The results of two independent experiments were merged. SAM analysis identified 116 relevant probe sets. Hierarchical clustering of these probe sets showed divergent early gene regulation by PDGF and FGF but overlapping late response. We first analyzed genes commonly regulated by PDGF-BB and b-FGF more than 2 fold after 24h of stimulation and we found that these two growth factors repressed FOXO. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
10 Samples
Download data: CEL, CHP
Series
Accession:
GSE14256
ID:
200014256
4.

FOXO target gene CTDSP2 inhibits cell cycle progression through regulation of p21-Cip1/Waf1

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL13183 GPL15789
32 Samples
Download data: TXT
Series
Accession:
GSE58987
ID:
200058987
5.

DK010: FOXO target gene CTDSP2 inhibits cell cycle progression through regulation of p21-Cip1/Waf1

(Submitter supplied) Activity of Forkhead box O (FOXO) transcription factors is inhibited by PI3K-PKB/Akt signalling to control a variety of cellular processes including cell cycle progression. Through comparative analysis of a number of microarray datasets, we identified a set of genes commonly regulated by FOXO and PI3K/PKB, which includes Carboxyl-Terminal Domain Small Phosphatase 2 (CTDSP2). We validated CTDSP2 as a genuine FOXO target gene and show that ectopic CTDSP2 can induce cell cycle arrest. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15789
12 Samples
Download data: TXT
Series
Accession:
GSE58986
ID:
200058986
6.

DK009: FOXO target gene CTDSP2 inhibits cell cycle progression through regulation of p21-Cip1/Waf1

(Submitter supplied) Activity of Forkhead box O (FOXO) transcription factors is inhibited by PI3K-PKB/Akt signalling to control a variety of cellular processes including cell cycle progression. Through comparative analysis of a number of microarray datasets, we identified a set of genes commonly regulated by FOXO and PI3K/PKB, which includes Carboxyl-Terminal Domain Small Phosphatase 2 (CTDSP2). We validated CTDSP2 as a genuine FOXO target gene and show that ectopic CTDSP2 can induce cell cycle arrest. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13183
8 Samples
Download data: TXT
Series
Accession:
GSE58947
ID:
200058947
7.

DK003: FOXO target gene CTDSP2 inhibits cell cycle progression through regulation of p21-Cip1/Waf1

(Submitter supplied) Activity of Forkhead box O (FOXO) transcription factors is inhibited by PI3K-PKB/Akt signalling to control a variety of cellular processes including cell cycle progression. Through comparative analysis of a number of microarray datasets, we identified a set of genes commonly regulated by FOXO and PI3K/PKB, which includes Carboxyl-Terminal Domain Small Phosphatase 2 (CTDSP2). We validated CTDSP2 as a genuine FOXO target gene and show that ectopic CTDSP2 can induce cell cycle arrest. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13183
4 Samples
Download data: TXT
Series
Accession:
GSE58945
ID:
200058945
8.

AS001: FOXO target gene CTDSP2 inhibits cell cycle progression through regulation of p21-Cip1/Waf1

(Submitter supplied) Activity of Forkhead box O (FOXO) transcription factors is inhibited by PI3K-PKB/Akt signalling to control a variety of cellular processes including cell cycle progression. Through comparative analysis of a number of microarray datasets, we identified a set of genes commonly regulated by FOXO and PI3K/PKB, which includes Carboxyl-Terminal Domain Small Phosphatase 2 (CTDSP2). We validated CTDSP2 as a genuine FOXO target gene and show that ectopic CTDSP2 can induce cell cycle arrest. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13183
8 Samples
Download data: TXT
Series
Accession:
GSE58909
ID:
200058909
9.

The ALK downregulated target gene HBP1 and repressor of MYCN activity as synergistic target for combined PI3K/HDAC inhibition

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL14550
16 Samples
Download data: TXT
Series
Accession:
GSE95193
ID:
200095193
10.

The ALK downregulated target gene HBP1 and repressor of MYCN activity as synergistic target for combined PI3K/HDAC inhibition [RNA-Seq]

(Submitter supplied) ALK mutations occur in 10% of primary neuroblastoma and represent a major target for precision treatment. In combination with MYCN amplification, ALK mutations infer an ultra-high-risk phenotype with very poor prognosis. To anticipate to future precision drugging, a deeper understanding of the molecular consequences of constitutive ALK signaling and its relationship to MYCN activity in this aggressive pediatric tumor, will be essential to understand treatment responses and failure as well as to ensure improved design of drugging combinations. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
12 Samples
Download data: TXT
Series
Accession:
GSE95189
ID:
200095189
11.

The ALK downregulated target gene HBP1 and repressor of MYCN activity as synergistic target for combined PI3K/HDAC inhibition [microarray]

(Submitter supplied) ALK mutations occur in 10% of primary neuroblastoma and represent a major target for precision treatment. In combination with MYCN amplification, ALK mutations infer an ultra-high-risk phenotype with very poor prognosis. To anticipate to future precision drugging, a deeper understanding of the molecular consequences of constitutive ALK signaling and its relationship to MYCN activity in this aggressive pediatric tumor, will be essential to understand treatment responses and failure as well as to ensure improved design of drugging combinations. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14550
4 Samples
Download data: TXT
Series
Accession:
GSE94811
ID:
200094811
12.

Gene expression profiling upon PI3K inhibition using different inhibitors

(Submitter supplied) Activation of the phosphoinositide 3-kinase (PI3K)/Akt signaling pathway is one the most frequent genetic events in human cancer. Therefore, the development of PI3K inhibitors has attracted much attention. We previously described the pyrazolopyrimidine derivative ETP-45658 as a potent inhibitor of PI3K p110α in vitro and in vivo. Here we report the gene expression signatures of MCF7 cells treated with ETP-45658 or the reference PI3K inhibitor PI-103. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
12 Samples
Download data: TXT
Series
Accession:
GSE56579
ID:
200056579
13.

FoxOs are lineage-restricted redundant tumor suppressors and regulate endothelial cell homeostasis.

(Submitter supplied) Activated phosphoinositide 3-kinase (PI3K)-AKT signaling appears to be an obligate event in the development of cancer. The highly related members of the mammalian FoxO transcription factor family, FoxO1, FoxO3, and FoxO4, represent one of several effector arms of PI3K-AKT signaling, prompting genetic analysis of the role of FoxOs in the neoplastic phenotypes linked to PI3K-AKT activation. While germline or somatic deletion of up to five FoxO alleles produced remarkably modest neoplastic phenotypes, broad somatic deletion of all FoxOs engendered a progressive cancer-prone condition characterized by thymic lymphomas and hemangiomas, demonstrating that the mammalian FoxOs are indeed bona fide tumor suppressors. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
14 Samples
Download data: CEL
Series
Accession:
GSE27932
ID:
200027932
14.

Cell culture-based model system for FOXO3 activity

(Submitter supplied) MCF7 and MDA-MB-231 breast cancer cell lines were cultured in DMEM-F12 containing 10% FBS (Lonza) 100U/ml penicillin and 100 µg/ml streptomycin (Lonza). Transfecting third generation packaging vectors using Poly-ethylenimine into HEK293T cells generated lentiviral particles (17). MCF7 and MDA-MB-231 cells were stably transduced with lentivirus containing pINDUCER20-FOXO3.A3, allowing doxycycline induced expression of constitutively active FOXO3 (FOXO3.A3). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24915
27 Samples
Download data: CEL
Series
Accession:
GSE113479
ID:
200113479
15.

Modulation of glutamine metabolism by the PI3K-PKB/c-akt-FOXO network regulates autophagy

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL14726
56 Samples
Download data: TXT
Series
Accession:
GSE35705
ID:
200035705
16.

CP003: Modulation of glutamine metabolism by the PI3K-PKB/c-akt-FOXO network regulates autophagy

(Submitter supplied) The PI3K-PKB/c-akt-FOXO signalling network provides a major intracellular hub for regulation of cell proliferation, survival and stress resistance1. Here we report a novel function for FOXO transcription factors in regulating autophagy through modulation of intracellular glutamine levels. To identify novel transcriptional targets of this module we performed an unbiased microarray analysis after conditional activation of the key components PI3K, PKB, FOXO3 and FOXO4. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL14726
16 Samples
Download data: TXT
Series
Accession:
GSE35703
ID:
200035703
17.

CP001: Modulation of glutamine metabolism by the PI3K-PKB/c-akt-FOXO network regulates autophagy

(Submitter supplied) The PI3K-PKB/c-akt-FOXO signalling network provides a major intracellular hub for regulation of cell proliferation, survival and stress resistance1. Here we report a novel function for FOXO transcription factors in regulating autophagy through modulation of intracellular glutamine levels. To identify novel transcriptional targets of this module we performed an unbiased microarray analysis after conditional activation of the key components PI3K, PKB, FOXO3 and FOXO4. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL14726
40 Samples
Download data: TXT
Series
Accession:
GSE35701
ID:
200035701
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