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Links from GEO DataSets

Items: 20

1.

ZEB1 expression prevents DNA replication stress in cancer stem cells and delays chromosomal instability [Agilent]

(Submitter supplied) Aberrant cell proliferation, a hallmark of most cancers, requires the escape from intrinsic antitumour barriers. Primary among these is the DNA damage response (DDR). In both cell culture-models and in early stages of tumorigenesis in vivo, activated oncogenes induce DNA replication stress and DNA double-strand breaks (DSBs), leading to DDR activation and p53-dependent apoptosis and/or senescence. The means by which tumour initiating cells, also termed cancer stem cells (CSCs), circumvent this oncosuppressive response is unknown. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL10123
15 Samples
Download data: TXT
Series
Accession:
GSE55989
ID:
200055989
2.

ZEB1 expression prevents DNA replication stress in cancer stem cells and delays chromosomal instability

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by array
Platforms:
GPL10123 GPL570
18 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE56031
ID:
200056031
3.

ZEB1 expression prevents DNA replication stress in cancer stem cells and delays chromosomal instability [Affymetrix]

(Submitter supplied) Aberrant cell proliferation, a hallmark of most cancers, requires the escape from intrinsic antitumour barriers. Primary among these is the DNA damage response (DDR). In both cell culture-models and in early stages of tumorigenesis in vivo, activated oncogenes induce DNA replication stress and DNA double-strand breaks (DSBs), leading to DDR activation and p53-dependent apoptosis and/or senescence. The means by which tumour-initiating cells, also termed cancer stem cells (CSCs), circumvent this oncosuppressive response is unknown. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
3 Samples
Download data: CEL, CHP
Series
Accession:
GSE55688
ID:
200055688
4.

EMT inducers catalyze malignant transformation of mammary epithelial cells and drive tumorigenesis towards claudin-low tumors

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL570 GPL1261
17 Samples
Download data: CEL, CHP
Series
Accession:
GSE32905
ID:
200032905
5.

EMT inducers catalyze malignant transformation of mammary epithelial cells and drive tumorigenesis towards claudin-low tumors [mouse]

(Submitter supplied) The newly identified claudin-low subtype of cancer is believed to represent the most primitive breast malignancies, having arisen from transformation of an early epithelial precursor with inherent stemness properties and metaplastic features. Challenging this hypothesis, we show both in vitro and in vivo that transcription factors inducing epithelial-mesenchymal transition can drive the development of claudin-low tumors from differentiated mammary epithelial cells, by playing a dual role in cell transformation and dedifferentiation.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
5 Samples
Download data: CEL, CHP
Series
Accession:
GSE32904
ID:
200032904
6.

EMT inducers catalyze malignant transformation of mammary epithelial cells and drive tumorigenesis towards claudin-low tumors [human]

(Submitter supplied) The newly identified claudin-low subtype of cancer is believed to represent the most primitive breast malignancies, having arisen from transformation of an early epithelial precursor with inherent stemness properties and metaplastic features. Challenging this hypothesis, we show both in vitro and in vivo that transcription factors inducing epithelial-mesenchymal transition can drive the development of claudin-low tumors from differentiated mammary epithelial cells, by playing a dual role in cell transformation and dedifferentiation.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL, CHP
Series
Accession:
GSE32727
ID:
200032727
7.

ΔNp63 promotes stem cell activity in mammary gland development and basal-like breast cancer by enhancing Fzd7 expression and Wnt signaling

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
20 Samples
Download data: TXT
Series
Accession:
GSE47493
ID:
200047493
8.

Transcriptome profiles of mouse mammary stem cells and progenitor cells

(Submitter supplied) MaSC, Luminal progenitor enriched subpopulations were isolated from virgin and pregnant mice based on using both surface marker or internal reporter transgene (GFP) expression. (Tiede BJ et al., 2009, PLoS ONE 4(11): e8035. doi:10.1371/journal.pone.0008035), and the transcirptome profiles were determined and compared.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
14 Samples
Download data: TXT
Series
Accession:
GSE47419
ID:
200047419
9.

∆Np63 regulates stem cell activity in mammary gland development

(Submitter supplied) MaSC, luminal progenitor enriched subpopulations and total MECs as well, were isolated from both wild type and ∆Np63 KO heterozygous mouse and the transcriptome profiles were determined and compared.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
6 Samples
Download data: TXT
Series
Accession:
GSE47417
ID:
200047417
10.

Molecular profiling of human mammary gland links breast cancer risk to a p27+ cell population with progenitor characteristics

(Submitter supplied) Gene expression, DNA and histone methylation profiles were performed on multiple cell types purified from normal human nulliparous and parous breast tissue using SAGE-seq, MSDK-seq and ChIP-seq [GSE26141].
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL9052
42 Samples
Download data: TXT
Series
Accession:
GSE32017
ID:
200032017
11.

Defining the role of ZEB1 in the pathogenesis of lung cancer

(Submitter supplied) Using an in vitro model for malignant transformation of human bronchial epithelial cells (HBECs) we have found epithelial-to-mesenchymal transition (EMT) and expression of the EMT-transcription factor ZEB1 are early and critical events. Specifically, we found preexisting oncogenic mutations in TP53 and KRAS were required for HBECs to engage EMT machinery in response to microenvironmental (serum/TGFβ) or specific oncogenetic (MYC) EMT-inducing factors, which induce EMT through distinct TGFβ-dependent and vitamin D receptor (VDR)-dependent pathways, respectively, with both requiring ZEB1. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
10 Samples
Download data: IDAT, TXT
Series
Accession:
GSE77925
ID:
200077925
12.

Identification of regions and genes important in Sézary syndrome pathogenesis using genomic and expression microarrays

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array; Expression profiling by array
Platforms:
GPL1266 GPL96 GPL2641
88 Samples
Download data: CEL
Series
Accession:
GSE17602
ID:
200017602
13.

Affymetrix Gene Expression array data for Sézary Syndrome (SS) samples

(Submitter supplied) This study used tumour and paired normal samples from 28 Sézary Syndrome (SS) patients to define recurrent regions of chromosomal aberrations. Our data identified recurrent losses of 17p13.2-p11.2 and 10p12.1-q26.3 occurring in 71 and 68% of cases respectively; common gains were detected for 17p11.2-q25.3 (64%) and chromosome 8/8q (50%). Moreover, we identified novel genomic lesions recurring in more than 30% of tumours: loss of 9q13-q21.33 and gain of 10p15.3-10p12.2. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
32 Samples
Download data: CEL
Series
Accession:
GSE17601
ID:
200017601
14.

Affymetrix SNP array data for Sézary Syndrome (SS) samples

(Submitter supplied) This study used tumour and paired normal samples from 28 Sézary Syndrome (SS) patients to define recurrent regions of chromosomal aberrations. Our data identified recurrent losses of 17p13.2-p11.2 and 10p12.1-q26.3 occurring in 71 and 68% of cases respectively; common gains were detected for 17p11.2-q25.3 (64%) and chromosome 8/8q (50%). Moreover, we identified novel genomic lesions recurring in more than 30% of tumours: loss of 9q13-q21.33 and gain of 10p15.3-10p12.2. more...
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platforms:
GPL1266 GPL2641
56 Samples
Download data: CEL
Series
Accession:
GSE17595
ID:
200017595
15.

RNA-sequencing in MDA-231-D cells transfected with ZEB1 or ZEB2 siRNAs

(Submitter supplied) We searched for roles of ZEB1and/or ZEB2 during EMT by RNA-seq in breast cancer cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17303
5 Samples
Download data: TXT
16.

ZEB1 binding sites in TGF-beta-stimulated MCF7 breast cancer cell line

(Submitter supplied) We searched for roles of ZEB1 during EMT through genome-wide analysis of its binding sites in breast cancer cells.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17303
1 Sample
Download data: BED, BW
Series
Accession:
GSE98270
ID:
200098270
17.

ZEB1-regulated inflammatory phenotype in breast cancer cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below. Zinc finger E-box binding protein 1 (ZEB1) and ZEB2 induce epithelial-mesenchymal transition (EMT) and cancer progression. However, little is known about global picture of transcriptional regulation by ZEB1 and ZEB2. Here we identified an inflammatory phenotype regulated by ZEB1 using chromatin immunoprecipitation-sequencing (ChIP-seq) and RNA-sequencing (RNA-seq) in basal type breast cancer cells, followed by gene set enrichment analysis (GSEA) of ZEB1-bound genes.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL17303
12 Samples
Download data: BED, BW
Series
Accession:
GSE89206
ID:
200089206
18.

RNA-sequencing in TGF-beta treated MDA-231-D cells transfected with ZEB1/ZEB2 siRNAs [RNA-seq]

(Submitter supplied) We searched for roles of ZEB1 during EMT by RNA-seq in breast cancer cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17303
4 Samples
Download data: TXT
19.

ZEB1 binding sites in TGF-beta-stimulated MDA-231-D and Hs578T basal type breast cancer cell lines [ChIP-seq]

(Submitter supplied) We searched for roles of ZEB1 during EMT through genome-wide analysis of its binding sites in breast cancer cells.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17303
2 Samples
Download data: BED, BW
Series
Accession:
GSE89203
ID:
200089203
20.

Gene Expression of murine mammary stem-like cells, HC11: Control vs miRNA206 mimic treatment

(Submitter supplied) MicroRNAs are likely to play pivotal roles in both stem cells and cancer, and are further promising candidates for future therapeutic purposes. To understand the role of miR206 in mammary cell differentiation, we profiled the transcription of mamary stem-like cells, comparing control HC11 cells (unspecific miRNA mimic treated) with HC11 cells transfected with miRNA-206 mimic.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21268
2 Samples
Download data: GPR
Series
Accession:
GSE76251
ID:
200076251
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