U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

β-catenin signaling is a critical event in ErbB2-mediated mammary tumor progression.

(Submitter supplied) Although ERBB2 amplification and overexpression is correlated with poor outcome in breast cancer, the molecular mechanisms underlying the aggressive nature of these tumors has not been fully elucidated. To investigate this further, we have used a transgenic mouse model of ErbB2-driven tumor progression (ErbB2KI model) that recapitulates clinically relevant events, including selective amplification of the core erbB2 amplicon. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL6585 GPL2872
18 Samples
Download data: TXT
Series
Accession:
GSE37954
ID:
200037954
2.

Gene expression from ErbB2KI tumors with a heterozygous or a homoszygous loss of beta-catenin (ctnnb1)

(Submitter supplied) Beta-catenin controls both cell adhesion and transcription to facilitate ErbB2-driven mammary tumorigenesis In this study, we used conditional knockout and gene expression approaches to understand global molecular and transciptional changes due to ablation of both functions of beta-catenin.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
15 Samples
Download data: CEL, CHP
Series
Accession:
GSE89498
ID:
200089498
3.

ATF3-induced mammary tumors exhibit molecular features of human basal-like breast cancer

(Submitter supplied) Transcriptional profiling of mammary tumors that occurs in parous, BK5.ATF3 mice, compared to adjacent normal mammary tissue
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: TXT
Series
Accession:
GSE162804
ID:
200162804
4.

BK5.ATF3-induced mammary tumors compared to normal mammary glands

(Submitter supplied) Transcriptional profiling of mammary tumors that occur in parous, BK5.ATF3 mice, compared to normal mammary tissue
Organism:
Murid gammaherpesvirus 4; Mus musculus; Murid betaherpesvirus 1
Type:
Non-coding RNA profiling by array
Platform:
GPL29478
7 Samples
Download data: GPR
Series
Accession:
GSE162793
ID:
200162793
5.

Expression data from Mammospheres

(Submitter supplied) The combined activation of Wnt/ß-catenin and MET/HGF is required for mammary cancer stem cell (MaCSC) maintenance. We generated mammospheres derived from tumors of mice harboring Wnt/Met signaling mutations on which we performed microarray analysis to evaluate gene expression signatures controlled by Wnt and MET pathways. We used the gene expression profiles to dissect the role and the functions of these pathways in MaCSCs.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
15 Samples
Download data: CEL
Series
Accession:
GSE35899
ID:
200035899
6.

SPARC knock down

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19507
20 Samples
Download data: GPR
Series
Accession:
GSE83832
ID:
200083832
7.

4T1 breast tumors: SPARC knock down primary tumors vs. Control primary tumors vs. Lung metastasis foci

(Submitter supplied) Comparative analysis of the transcriptome of primary tumors generated from 4T1 cells transduced with a lentiviral vector expressing a siRNA against murine SPARC (4T1-C18), primary tumors generated from 4T1 cells transduced with a lentiviral vector expressing a scramble sequence (4T1-SCR) or lung metastasis foci from 4T1-SCR tumor-bearing mice (4T1-SCR MTTS).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19507
12 Samples
Download data: GPR
Series
Accession:
GSE83831
ID:
200083831
8.

4T1 breast cancer cells: SPARC knock down vs. Control

(Submitter supplied) Comparative analysis of the transcriptome of 4T1 cells stably transduced with a lentiviral vector expressing a siRNA against murine SPARC (4T1-C18) with 4T1 control cells stably transduced with a lentiviral vector expressing a scramble sequence (4T1-SCR).
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19507
8 Samples
Download data: GPR
Series
Accession:
GSE83830
ID:
200083830
9.

Copy number aberrations in mouse breast tumors reveal loci and genes important in tumorigenic RTK signaling

(Submitter supplied) Receptor tyrosine kinase (RTK) signaling plays a key role in the development of breast cancer. Defining the genes and pathways in the RTK signaling network that are important regulators of tumorigenesis in vivo will unveil potential candidates for targeted therapeutics. To this end, we utilized microarray comparative genomic hybridization (array CGH) to identify and compare copy number aberrations in 5 mouse models of breast cancer induced by wild-type and mutated forms of oncogenic ErbB2 or the polyomavirus middle T antigen (PyMT). more...
Organism:
Mus musculus
Type:
Genome variation profiling by genome tiling array
5 related Platforms
166 Samples
Download data
Series
Accession:
GSE3012
ID:
200003012
10.

Elevated expression of wildtype RhoC promotes ErbB2- and Pik3ca-induced mammary tumor formation

(Submitter supplied) Copy number gains in genes coding for Rho activating exchange factors as well as losses affecting genes coding for RhoGAP proteins are common in breast cancer, suggesting that elevated Rho signaling may play an important role. Extra copies and overexpression of RhoC also occur, although a role for RhoC overexpression in driving tumor formation has not been assessed in vivo. To this end, we report on the development of a Rosa26 (R26)-targeted Cre-conditional RhoC overexpression mouse (R26-RhoC). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
21 Samples
Download data: TSV, TXT
Series
Accession:
GSE249601
ID:
200249601
11.

Transcriptome profiling of breast cancer cells with Insulin like growth factor binding protein 2 (IGFBP2) knockdown

(Submitter supplied) The study was carried out to identify the genes regulated upon IGFBP2 modulation in breast cancer. This will help to understand the molecular targets and biological pathways targeted by IGFBP2 in breast cancer.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
4 Samples
Download data: TXT
Series
Accession:
GSE40682
ID:
200040682
12.

Role of CSN5 in breast cancer

(Submitter supplied) CSN5 has been implicated as a candidate oncogene in human breast cancers by genetic linkage with activation of the poor-prognosis, wound response gene expression signature. CSN5 is a subunit of the eight-protein COP9 signalosome, a signaling complex with multiple biochemical activities; the mechanism of CSN5 action in cancer development remains poorly understood. Here we show that CSN5 isopeptidase activity is essential for breast epithelial transformation and progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by array
Platform:
GPL5620
13 Samples
Download data
Series
Accession:
GSE9206
ID:
200009206
13.

Role of CSN5 in breast cancer (array CGH)

(Submitter supplied) CSN5 has been implicated as a candidate oncogene in human breast cancers by genetic linkage with activation of the poor-prognosis, wound response gene expression signature. CSN5 is a subunit of the eight-protein COP9 signalosome, a signaling complex with multiple biochemical activities; the mechanism of CSN5 action in cancer development remains poorly understood. Here we show that CSN5 isopeptidase activity is essential for breast epithelial transformation and progression. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL5620
5 Samples
Download data
Series
Accession:
GSE9205
ID:
200009205
14.

Role of CSN5 in breast cancer (siRNA transfections)

(Submitter supplied) CSN5 has been implicated as a candidate oncogene in human breast cancers by genetic linkage with activation of the poor-prognosis, wound response gene expression signature. CSN5 is a subunit of the eight-protein COP9 signalosome, a signaling complex with multiple biochemical activities; the mechanism of CSN5 action in cancer development remains poorly understood. Here we show that CSN5 isopeptidase activity is essential for breast epithelial transformation and progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5620
8 Samples
Download data
Series
Accession:
GSE9204
ID:
200009204
15.

A Syngeneic ErbB2 Mammary Cancer Model for Preclinical Immunotherapy Trials

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL11002 GPL6246
12 Samples
Download data: CEL, TXT
Series
Accession:
GSE113380
ID:
200113380
16.

A Syngeneic ErbB2 Mammary Cancer Model for Preclinical Immunotherapy Trials [RNA-seq]

(Submitter supplied) A cell line was derived from a mammary carcinoma in the transgenic FVB/N-Tg(MMTV-ErbB2)NDL2-5Mul mouse. The line, referred to as “NDL(UCD)” is adapted to standard cell culture and can be transplanted into syngeneic FVB/N mice. The line maintains a stable phenotype over multiple in vitro passages and rounds of in vivo transplantation. The cell line exhibits high expression of ErbB2 and ErbB3 and signaling molecules downstream from ErbB2. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
3 Samples
Download data: TXT
Series
Accession:
GSE113379
ID:
200113379
17.

A Syngeneic ErbB2 Mammary Cancer Model for Preclinical Immunotherapy Trials [microarray]

(Submitter supplied) A cell line was derived from a mammary carcinoma in the transgenic FVB/N-Tg(MMTV-ErbB2)NDL2-5Mul mouse. The line, referred to as “NDL(UCD)” is adapted to standard cell culture and can be transplanted into syngeneic FVB/N mouse. The line maintains stable phenotype over multiple in vitro passages and rounds of in vivo transplantation. The cell line exhibits high expression of ErbB2 and ErbB3 and signaling molecules downstream ErbB2. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
9 Samples
Download data: CEL
Series
Accession:
GSE112723
ID:
200112723
18.

Pygopus2-Histone interaction is important for de-differentiation and breast cancer progression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
32 Samples
Download data: BEDGRAPH
Series
Accession:
GSE133068
ID:
200133068
19.

Pygopus2-Histone interaction is important for de-differentiation and breast cancer progression [ATAC-Seq]

(Submitter supplied) Pygopus2 (Pygo2), a co-activator of Wnt/ β-catenin signaling can also bind H3K4me2/3 and participate in chromatin reading and writing. To investigate the functional relevance of histone binding activity of Pygo2 in malignant progression of breast cancer, we generated a knockin mouse model wherein binding of Pygo2 to H3K4me2/3 was rendered ineffective. Loss of Pygo2-histone binding resulted in smaller, differentiated and less metastatic tumors, at least in part due to a decrease in Wnt/ b-catenin signaling. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL19057
16 Samples
Download data: BEDGRAPH
Series
Accession:
GSE133066
ID:
200133066
20.

Pygopus2-Histone interaction is important for de-differentiation and breast cancer progression [RNA-Seq]

(Submitter supplied) Pygopus2 (Pygo2), a co-activator of Wnt/ β-catenin signaling can also bind H3K4me2/3 and participate in chromatin reading and writing. To investigate the functional relevance of histone binding activity of Pygo2 in malignant progression of breast cancer, we generated a knockin mouse model wherein binding of Pygo2 to H3K4me2/3 was rendered ineffective. Loss of Pygo2-histone binding resulted in smaller, differentiated and less metastatic tumors, at least in part due to a decrease in Wnt/ b-catenin signaling. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
16 Samples
Download data: TXT
Series
Accession:
GSE130330
ID:
200130330
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=5|blobid=MCID_677ec7ef7eb86f557f1600cb|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center