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Links from GEO DataSets

Items: 20

1.

S100A4+ Stromal Cells from Normal Lung vs. Metastatic Lung

(Submitter supplied) Analysis of S100A4+ stromal cells at the gene expression level in physiological setting versus metastatic setting.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
2 Samples
Download data: TXT
Series
Accession:
GSE31711
ID:
200031711
2.

Effect of extracellular S100A4 on melanoma cells of different phenotypes

(Submitter supplied) S100A4 is a known metastasis-promoting factor, rich in the tumor microenvironment. To clarify how extracellular S100A4 execute its pro-metastatic function, we analyzed gene expression in melanoma cells stimulated with recombinant protein rS100A4 and compared it to the expression in control non-stimulated cells. Two melanoma cell lines representing two distinct phenotypes – invasive (Melmet 1) and non-invasive/proliferative (Melmet 5) – were included in the study. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE65897
ID:
200065897
3.

Integrin alpha6-beta4 control the expression of genes associated with cell motility, invasion and metastasis

(Submitter supplied) The objective of this study was to determine the gene expression changes mediated by the alpha6beta4 integrin using MDA-MB-435 breast carcinoma cell line under normal culturing conditions (10% FCS in DMEM). Keywords: Transfection (stable)
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
8 Samples
Download data: CEL, CHP
Series
Accession:
GSE11466
ID:
200011466
4.

CRISPR/Cas9 knock down line

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Expression profiling by high throughput sequencing
Platforms:
GPL17021 GPL21103 GPL4134
22 Samples
Download data: TXT
Series
Accession:
GSE126351
ID:
200126351
5.

study CRISPR/Cas9 knock down line by RNA-seq

(Submitter supplied) validate and study CRISPR/Cas9 knock down line by RNA-seq
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: TXT
Series
Accession:
GSE126350
ID:
200126350
6.

Study gene expression in mouse mammary tumors single cell RNA-seq, study CRISPR/Cas9 knock down line by RNA-seq

(Submitter supplied) Study gene expression in mouse mammary tumors single cell RNA-seq, study CRISPR/Cas9 knock down line by RNA-seq
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
8 Samples
Download data: TXT
Series
Accession:
GSE126349
ID:
200126349
7.

Study differentially expressed genes comparing metastatic sarcomatoid carcinomas vs adenocarcinomas

(Submitter supplied) compare expression of two groups of tumors
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
10 Samples
Download data: TXT
Series
Accession:
GSE126348
ID:
200126348
8.

Expression data from non-metastatic and metastatic osteosarcoma cells

(Submitter supplied) Osteosarcoma (OS) is the malignant bone tumor with a high tendency to metastasize to the lung, where the molecular mechanisms are unclear. The mouse OS cell line LM8 has been isolated originally from the Dunn OS cell line by in vivo selection as a subline with a high metastatic potential to the lung. We used gene chip-based global gene expression analysis of differential screening between parental Dunn and LM8 cells in order to reveal genes predominantly expressed in LM8 cells, which correlate with high metastatic potential.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL, EXP
Series
Accession:
GSE26648
ID:
200026648
9.

Expression data from human breast cancer cells MCF-7 before and after ATP treatment

(Submitter supplied) We used microarrays to explore gene expression fold change in breast cancer cells before and after ATP treatment.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE113757
ID:
200113757
10.

Gene expression compare between liver cancer associated mesenchymal stem cells (LC8-MSC) and liver normal mesenchymal stem cells (LN8-MSC)

(Submitter supplied) Transcriptional profiling of liver cancer associated mesenchymal stem cells comparing normal mesenchymal stem cells from adjacent tumor-free tissues of the same patient 8, Goal was to determine to detect the paracrine trophic factors from liver cancer mesenchymal stem cells. 8 represents liver cancer associated MSCs, N8 represents liver normal MSCs
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
1 Sample
Download data: TXT
Series
Accession:
GSE42357
ID:
200042357
11.

Osteosarcoma cells-derived secretome induce pre-metastatic changes in the lung microenvironment that support lung metastasis formation

(Submitter supplied) To investigate the molecular and cellular alterations occurring in the lung tissue during the pre-metastatic niche formation in osteosarcoma, we used two different approaches in which mice were implanted subcutaneously with the 143B OS cells for a primary tumour (PT) formation or treated with the 143B cell-derived secretome (SCR) to mimic the release of secreted factors by a locally primary tumour.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
15 Samples
Download data: XLSX
Series
Accession:
GSE216744
ID:
200216744
12.

Transcriptomic profiling of bone marrow-derived macrophages upon treatment with recombinant Tenascin-C and TLR4 inhibitor

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
9 Samples
Download data: CEL
Series
Accession:
GSE184299
ID:
200184299
13.

Transcriptomic profiling of mouse lung endothelial cells associated with metastasis of Tenascin C-depleted breast cancer cells

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE184298
ID:
200184298
14.

Transcriptomic profiling of SUM159 human breast cancer cells with ectopic expression of SCGB3A1

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE184296
ID:
200184296
15.

Inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL1261 GPL570
63 Samples
Download data: CEL
Series
Accession:
GSE156354
ID:
200156354
16.

Transcriptomic profiling of SUM-LM1 human breast cancer cells upon treatment with recombinant Activin B or vehicle

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE156353
ID:
200156353
17.

Transcriptomic profiling of metastasis-associated lung endothelial cells from mice with treatment for macrophage-depletion

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
6 Samples
Download data: CEL
Series
Accession:
GSE156352
ID:
200156352
18.

Transcriptomic profiling of metastasis-associated lung endothelial cells from mice treated with anti-VEGFA antibody (B20.4.1.1)

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
9 Samples
Download data: CEL
Series
Accession:
GSE156351
ID:
200156351
19.

Transcriptomic profiling of metastasis-associated lung endothelial cells from mice treated with anti-VEGFR2 antibody (DC101)

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
9 Samples
Download data: CEL
Series
Accession:
GSE156350
ID:
200156350
20.

Transcriptomic profiling of lung endothelial cells at different stages of lung colonization by MDA-MB-231-LM2 cells

(Submitter supplied) In cancer progression to metastasis, disseminated cancer cells frequently lodge near vasculature in secondary organs. However, our understanding of the cellular crosstalk evoked at perivascular sites is still rudimentary. In this study, we identified an inter-cellular machinery governing formation of a pro-metastatic vascular niche during breast cancer colonization in lungs. Transcriptomic analysis of endothelial cells (ECs) isolated from mouse lungs with metastases revealed a marked upregulation of genes linked to proliferation, inflammation and numerous secreted proteins. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE156349
ID:
200156349
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