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Links from GEO DataSets

Items: 18

1.
Full record GDS5323

CREB-Binding Protein Inhibitor ICG-001 effect on pancreatic cancer cell line: time course

Analysis of AsPC1 pancreatic adenocarcinoma (PDAC) cells treated with IGC-001 up to 24 hours. IGC-001 binds to CREB-binding protein to disrupt its interaction with β-catenin. Results compared to β-catenin depletion (GDS5324) and provide insight into the therapeutic potential of IGC-001 in PDAC.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 2 time sets
Platform:
GPL570
Series:
GSE57728
12 Samples
Download data: CEL
2.

Expression data from AsPC1 cells treated with ICG-001

(Submitter supplied) The CREB binding protein inhibitor ICG-001 suppresses pancreatic cancer growth We used microarrays to detail global gene expression changes in the pancreatic cancer cell line AsPC1 following treatment with ICG-001 or siRNA-mediated knockdown of CTNNB1 (beta-catenin)
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS5323 GDS5324
Platform:
GPL570
16 Samples
Download data: CEL
Series
Accession:
GSE57728
ID:
200057728
3.
Full record GDS5324

Beta-catenin depletion effect on pancreatic cancer cell line

Analysis of AsPc1 pancreatic adenocarcinoma cells depleted for beta-catenin. Dysregulation of Wnt/β-catenin signaling is implicated in the pathogenesis of cancers. Results compared to those from AsPC1 cells treated with the CREB-binding protein inhibitor ICG-001 (GDS5323).
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL570
Series:
GSE57728
4 Samples
Download data: CEL
4.

Targeting oncogenic β-catenin/CBP activity for the treatment of head and neck squamous cell carcinoma

(Submitter supplied) Head and neck squamous cell carcinoma (HNSCC) presents primarily as oral squamous cell carcinoma (OSCC), an aggressive malignancy characterized by heterogeneity, locoregional metastases and resistance to existing treatments. Although a number of molecular alterations associated with OSCC have been identified, they have had limited impact on clinical management. A frequent feature of OSCC is the inappropriate activation of nuclear β-catenin. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17930
18 Samples
Download data: CEL
Series
Accession:
GSE95704
ID:
200095704
5.

Crizotinib inhibits metabolic inactivation of gemcitabine in ortothopic pancreatic tumors derived from primary cells with c-Met overexpression

(Submitter supplied) Pancreatic ductal adenocarcinoma (PDAC) remains a major unsolved health problem. Most drugs that pass preclinical tests fail in these patients, emphasizing the need of appropriate preclinical models to test novel anticancer strategies. We developed four orthotopic mouse models employing primary human PDAC cells expressing Firefly and Gaussia luciferases, enabling bioluminescence monitoring of tumor growth and metastasis formation. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL16694
8 Samples
Download data: TXT
Series
Accession:
GSE44587
ID:
200044587
6.

Regulation of gene expression in uveal melanoma cells by ICG-001

(Submitter supplied) We examined the effects of ICG-001 on gene expression in Mel202 uveal melanoma (UM) cells. ICG-001 exerted strong antiproliferative activity against UM cells, leading to cell cycle arrest, apoptosis, and inhibition of migration. Global gene expression profiling revealed strong suppression of genes associated with cell cycle proliferation, DNA replication, and G1/S transition. Gene set enrichment analysis revealed that ICG-001 suppressed Wnt, mTOR, and MAPK signaling. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
14 Samples
Download data: TXT
Series
Accession:
GSE149417
ID:
200149417
7.

The gamma secretase inhibitor MRK-003 attenuates pancreatic cancer growth in preclinical models

(Submitter supplied) Pancreatic ductal adenocarcinoma (PDAC) is a nearly uniformly lethal malignancy, with most patients facing an adverse clinical outcome. Given the pivotal role of aberrant Notch signaling in the initiation and progression of PDAC, we investigated the effect of MRK-003, a potent and selective γ-secretase inhibitor, in preclinical PDAC models. We used a panel of human PDAC cell lines, as well as patient-derived PDAC xenografts, to determine whether pharmacological targeting of the Notch pathway could inhibit pancreatic tumor growth and potentiate gemcitabine sensitivity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4342
Platform:
GPL570
18 Samples
Download data: CEL
Series
Accession:
GSE37645
ID:
200037645
8.
Full record GDS4342

Gamma secretase inhibitor MRK-003 effect on pancreatic ductal adenocarcinoma tumor xenografts

Analysis of 9 individual patient-derived, pancreatic ductal adenocarcinoma (PDAC) xenografts treated with GSI MRK-003. MRK-003 monotherapy significantly reduced tumor volume in 5 of 9 xenografts. Results provide insight into the molecular basis of MRK-003-mediated attenuation of PDAC.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 9 cell line, 2 other sets
Platform:
GPL570
Series:
GSE37645
18 Samples
Download data: CEL
9.

Pharmacological modulation of the Wnt/β-catenin pathway inhibits the proliferation of long-lived latently-infected memory CD4+ T-cells in ART-suppressed SIV-infected macaques

(Submitter supplied) The major obstacle to human immunodeficiency type 1 (HIV-1) eradication is a reservoir of latently-infected cells that persists despite long-term antiretroviral therapy (ART) and is maintained through cellular proliferation. Long-lived memory CD4+ T-cells with high self-renewal capacity such as central memory T-cells (CM) and T memory stem cells (SCM) are major contributors to the viral reservoir in HIV-infected individuals on ART. more...
Organism:
Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23804
47 Samples
Download data: TXT
Series
Accession:
GSE127330
ID:
200127330
10.

Analyses of mIRNA transcript level following exposure to triptolide

(Submitter supplied) Analyses of mirna transcript levels following exposure to the drug triptolide in vitro and prodrug minnelide in xenograft pancreatic tumor mouse models.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8179
42 Samples
Download data: TXT
Series
Accession:
GSE46188
ID:
200046188
11.

Change in expression of genes after retinoic acid treatment of stellate cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6102
41 Samples
Download data: TXT
Series
Accession:
GSE14427
ID:
200014427
12.

Change in expression of genes after retinoic acid treatment of stellate cells: time course

(Submitter supplied) We evaluated the change in expression of genes after treatment of stellate cells with retinoic acid to understand how the stellate cells can de-differentiate and effect their physiological behaviour in pathological conditions. We then tested the changes in the gene expression in 2D and 3D culture conditions for pancreatic stellate cells and in a pancreatic cancer model. Keywords: gene expression change, time course
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6102
30 Samples
Download data: TXT
Series
Accession:
GSE14426
ID:
200014426
13.

Change in expression of genes after retinoic acid treatment of stellate cells: dose response

(Submitter supplied) We evaluated the change in expression of genes after treatment of stellate cells with retinoic acid to understand how the stellate cells can de-differentiate and effect their physiological behaviour in pathological conditions. We then tested the changes in the gene expression in 2D and 3D culture conditions for pancreatic stellate cells and in a pancreatic cancer model. Keywords: gene expression change, dose response, matrix conditions
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6102
11 Samples
Download data: TXT
Series
Accession:
GSE14425
ID:
200014425
14.

Inhibition of histone acetyltransferase attenuates 3D chromatin-mediated insulin signaling in pancreatic cancer (RNAseq dataset)

(Submitter supplied) Inhibition of histone acetyltransferase has been widely used to be effectively treat cancers in many studies. However, it’s not clear how the downstream signaling responds to the inhibitor in pancreatic cancer. Here we performed Hi-C experiments and RNA-seq to canonical and patient-derived pancreatic cancer cells with the treatment of small molecule inhibitor ICG-001 which has dual function to block both WNT signaling and histone acetyltransferase. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
24 Samples
Download data: TXT
Series
Accession:
GSE198444
ID:
200198444
15.

Inhibition of histone acetyltransferase attenuates 3D chromatin-mediated insulin signaling in pancreatic cancer (Hi-C dataset)

(Submitter supplied) Inhibition of histone acetyltransferase has been widely used to be effectively treat cancers in many studies. However, it’s not clear how the downstream signaling responds to the inhibitor in pancreatic cancer. Here we performed Hi-C experiments to canonical and patient-derived pancreatic cancer cells with the treatment of small molecule inhibitor ICG-001 which has dual function to block both WNT signaling and histone acetyltransferase. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL21290
8 Samples
Download data: TXT
Series
Accession:
GSE197293
ID:
200197293
16.

To determine the differentially expressed genes in cancer associated fibroblasts upon ablation of the glutamatergic synapse protein NetrinG1.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL13497 GPL16791
12 Samples
Download data: TXT
Series
Accession:
GSE156964
ID:
200156964
17.

To determine the differentially expressed genes in cancer associated fibroblasts upon ablation of the glutamatergic synapse protein NetrinG1. [RNA-Seq]

(Submitter supplied) Purpose: To determine the differentially expressed genes in cancer associated fibroblasts upon ablation of the glutamatergic synapse protein NetrinG1. Methods: Cancer associated fibroblast mRNA profiles were generated from Control and NetrinG1 KO fibroblast lines, with controls done in duplicate and KOs in triplicate. Results: Comparing the mRNA profiles of CON and NetrinG1 KO CAFs, we observed a reversion of many pro-tumor genes and associated pathways upon ablation of NetrinG1 in CAFs. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
8 Samples
Download data: TXT
18.

To determine the differentially expressed genes in cancer associated fibroblasts upon ablation of the glutamatergic synapse protein NetrinG1. [Microarray]

(Submitter supplied) Cancer associated fibroblast mRNA profiles were generated from Control and NetrinG1 KO fibroblast lines, with controls done in duplicate and KOs in triplicate. Comparing the mRNA profiles of CON and NetrinG1 KO CAFs, we observed a reversion of many pro-tumor genes and associated pathways upon ablation of NetrinG1 in CAFs.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13497
4 Samples
Download data: TXT
Series
Accession:
GSE156962
ID:
200156962
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