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Links from GEO DataSets

Items: 17

1.

RNA-seq of NIC AXL KO in hypoxia

(Submitter supplied) RNA-seq of MMTV-NIC WT and AXL KO cells in normoxia and hypoxia (1% O2)
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT, XLSX
Series
Accession:
GSE158583
ID:
200158583
2.

The Receptor Tyrosine Kinase AXL is Required at Multiple Steps of the Metastatic Cascade during HER2-positive Breast Cancer Progression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
10 Samples
Download data: TXT
Series
Accession:
GSE102370
ID:
200102370
3.

RNA-seq of MMTV-Neu AXL KO tumor grafts in FVB

(Submitter supplied) AXL is activated by its ligand GAS6 and is expressed in triple-negative breast cancer cells. We report that AXL is also detected in HER2+ breast cancer specimens where its expression correlates with poor patients’ survival. Using murine models of HER2+ breast cancer, AXL, but not Gas6, was found essential for metastasis. We determined that AXL is required for intravasation, extravasation and growth at the metastatic site. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: TXT
Series
Accession:
GSE102369
ID:
200102369
4.

RNA-seq of MMTV-Neu AXL KO tumors

(Submitter supplied) AXL is activated by its ligand GAS6 and is expressed in triple-negative breast cancer cells. We report that AXL is also detected in HER2+ breast cancer specimens where its expression correlates with poor patients’ survival. Using murine models of HER2+ breast cancer, AXL, but not Gas6, was found essential for metastasis. We determined that AXL is required for intravasation, extravasation and growth at the metastatic site. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT, XLSX
Series
Accession:
GSE102368
ID:
200102368
5.

Transcriptomic analysis of orthotopic pancreatic tumors treated by Axl inhibitor TP-0903 or combination with chemo/immunotherapy using the nCounter PanCancer Immune Profiling panel (Nanostring Technologies) [mouse]

(Submitter supplied) RNA isolated from KPfC orthotopic tumors was analyzed using Mouse PanCancer Immune Profiling Panel (NanoString Technologies).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL30298
36 Samples
Download data: CSV, RCC
Series
Accession:
GSE185110
ID:
200185110
6.

The role of vimentin in regulating genes related to EMT

(Submitter supplied) To study the biological and functional role of vimentin in maintenance of the mesenchymal phenotype of mammary epithelial cells, vimentin was silenced in the non-transformed MCF10A cells and vimentin-dependent changes in gene expression were analyzed.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6106
4 Samples
Download data: TXT
Series
Accession:
GSE17802
ID:
200017802
7.

An epithelial-mesenchymal transition (EMT) gene signature predicts resistance to erlotinib and PI3K pathway inhibitors and identifies Axl as a novel EMT marker in non-small cell lung cancer.

(Submitter supplied) Epithelial/mesenchymal transition (EMT) is associated with loss of cell adhesion molecules, such as E-cadherin, and increased invasion, migration, and proliferation in epithelial cancers. In non-small cell lung cancer (NSCLC), EMT is associated with greater resistance to EGFR inhibitors. However, its potential to predict response to other targeted drugs or chemotherapy has not been well characterized. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
131 Samples
Download data: CEL
Series
Accession:
GSE33072
ID:
200033072
8.

Expression profiling of lung cancer cell lines (UTSW Lung Panel V2)

(Submitter supplied) Epithelial/mesenchymal transition (EMT) is associated with loss of cell adhesion molecules, such as E-cadherin, and increased invasion, migration, and proliferation in epithelial cancers. In non-small cell lung cancer (NSCLC), EMT is associated with greater resistance to EGFR inhibitors. However, its potential to predict response to other targeted drugs or chemotherapy has not been well characterized. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13376
69 Samples
Download data: TXT
Series
Accession:
GSE32989
ID:
200032989
9.

Expression profiling of lung cancer cell lines

(Submitter supplied) Purpose: To determine the 8-week disease control rate (DCR) of sorafenib monotherapy in patients with advanced non-small-cell lung cancer (NSCLC) in the BATTLE trial. Methods: Patients with pre-treated NSCLC, ECOG performance status (PS) 0-2, consented to biopsies to test for biomarker assessment. Sorafenib was given at 400 mg orally twice daily until tumor progression or an unacceptable toxicity. Tumor evaluations were performed at baseline and every 8 weeks. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL10558 GPL6884
222 Samples
Download data: TXT
Series
Accession:
GSE32036
ID:
200032036
10.

Expression data from MCF-7 and MCF-7/ADR cells

(Submitter supplied) Chemoresistance in breast cancer has been a great interest in past studies, however, the development of rational therapeutic strategies targeting chemoresistant cells is still a challenge for clinical oncology.The resistant property of MCF7/ADR cells was confirmed by long term culture with Dox, cell viability, and PARP cleavage assays. Microarray analysis was performed to compare the global differences of gene expression between MCF-7 and MCF-7/ADR cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE76540
ID:
200076540
11.

Identification of the receptor tyrosine kinase AXL in triple negative breast cancer as a novel target for the human miR-34a microRNA

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus; Homo sapiens; Mus musculus
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL5106 GPL570
21 Samples
Download data: CEL, GPR
Series
Accession:
GSE21834
ID:
200021834
12.

Identification of the receptor tyrosine kinase AXL in triple negative breast cancer as a novel target for the human miR-34a microRNA (gene expression)

(Submitter supplied) Triple negative breast cancer (TNBC) is histologically characterized by the absence of the hormone receptors estrogen and progesterone, in addition to having a negative immunostain for HER-2. The aggressiveness of this disease and lack of targeted therapeutic options for treatment is of high clinical importance. MicroRNAs are short 21- to 23 nucleotide endogenous non-coding RNAs that regulate gene expression by binding to mRNA transcripts, resulting in either decreased protein translation or mRNA degradation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
9 Samples
Download data: CEL
Series
Accession:
GSE21832
ID:
200021832
13.

Identification of the receptor tyrosine kinase AXL in triple negative breast cancer as a novel target for the human miR-34a microRNA (miRNA study)

(Submitter supplied) Triple negative breast cancer (TNBC) is histologically characterized by the absence of the hormone receptors estrogen and progesterone, in addition to having a negative immunostain for HER-2. The aggressiveness of this disease and lack of targeted therapeutic options for treatment is of high clinical importance. MicroRNAs are short 21- to 23 nucleotide endogenous non-coding RNAs that regulate gene expression by binding to mRNA transcripts, resulting in either decreased protein translation or mRNA degradation. more...
Organism:
Rattus norvegicus; Homo sapiens; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL5106
12 Samples
Download data: GPR
Series
Accession:
GSE21719
ID:
200021719
14.

Mesenchymal cancer cell-stromal crosstalk promotes niche activation, epithelial reversion and metastatic colonization

(Submitter supplied) The experiment was design to address the intrinsic differences between metastatic cancer stem cells in the primary tumour and during metastatic colonization in the mouse mammary gland tumour model MMTV-pyMT.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
3 Samples
Download data: TXT
Series
Accession:
GSE63558
ID:
200063558
15.

Differential gene expression in MCF10A cells upon stable co-upregulation of flotillins 1 and 2

(Submitter supplied) The simultaneous overexpression of flotillins 1 and 2 is observed in many cancers and considered as a marker of poor prognosis, notably in breast cancer. Flotillin-overexpression was shown to participate in the invasive behavior of cancer cell leading to metastasis. To better characterize the specific contribution of flotillin upregulation in the acquisition of cellular invasive properties, we stably expressed at high level exogenous flotillin 1 (HA-tagged) and flotillin 2 (mCherry tagged) in the non-tumoral mammary epithelial MCF10A human cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
6 Samples
Download data: CSV
Series
Accession:
GSE190176
ID:
200190176
16.

RNA sequencing of CD19-directed chimeric antigen receptor T (CART19) cells with and without TP-0903 treatment

(Submitter supplied) TP-0903 was obtained from Tolero Pharmaceuticals. CART19 cells from five biological replicates were thawed and stimulated with irradiated Jeko-1 cells (120 Gy) for 5 days. Jeko-1 is a human mantle cell lymphoma cell line that expresses the CD19 antigen (ATCC). Each sample was treated with either 30 nM TP0903 (treated condition) or DMSO (untreated control). CART19 were isolated to a purity of 100% using CD19 microbeads (Miltenyi). more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
10 Samples
Download data: CSV, TXT
Series
Accession:
GSE199257
ID:
200199257
17.

Effects of PFKFB4 deletion on transcriptional reprogramming in breast cancer cells

(Submitter supplied) To explore the mechanisms by which PFKFB4 promotes breast cancer metastasis, we CRISPR-Cas knock-out PFKFB4 in two breast cancer lines for RNA-seq to identify downstream target genes that are regulated by PFKFB4
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24247 GPL24676
12 Samples
Download data: CSV
Series
Accession:
GSE217132
ID:
200217132
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