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Links from GEO DataSets

Items: 19

1.

Gene expression profiling in T-47D breast cancer cells following inducible expression of estrogen receptor beta

(Submitter supplied) T-47D breast cancer cells were stably transfected with a tet-off inducible construct encoding estrogen receptor beta. Microarray experiments were carried out at multiple time points 1-30 hours following treatment with estradiol and under induction and non-induction conditions. Keywords: Inducible expression of ERbeta
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4840
20 Samples
Download data: GPR
Series
Accession:
GSE7206
ID:
200007206
2.

Estrogen receptor beta expression is associated with tamoxifen response in ER alpha-negative breast carcinoma

(Submitter supplied) Purpose: Endocrine therapies, such as tamoxifen are commonly given to most patients with estrogen receptor (ER) alpha-positive breast carcinoma but are not indicated for persons with ERalpha-negative cancer. The factors responsible for response to tamoxifen in 5-10% of patients with ERalpha-negative tumors are not clear. The aim of the present study was to elucidate the biology and role of the second ER, ERbeta, in patients treated with adjuvant tamoxifen. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2827
Platform:
GPL3883
88 Samples
Download data: GPR
Series
Accession:
GSE6577
ID:
200006577
3.
Full record GDS2827

ERalpha-negative ERbeta-positive breast carcinoma response to tamoxifen

Analysis of estrogen receptor (ER) alpha negative ERbeta-positive breast cancer tumors from patients treated with tamoxifen for 2 years. Unlike ERalpha-negative ERbeta-negative breast cancers, ERalpha-negative ERbeta-positive cancers respond favorably to tamoxifen treatment.
Organism:
Homo sapiens
Type:
Expression profiling by array, log2 ratio, 6 specimen sets
Platform:
GPL3883
Series:
GSE6577
88 Samples
Download data: GPR
4.

Estrogen-regulated genes predict survival in estrogen receptor and/or progesterone receptor-positive breast cancers

(Submitter supplied) The prognosis of a patient with Estrogen Receptor (ER) and/or Progesterone Receptor (PR)-positive breast cancer is highly variable. Therefore, we developed a gene-expression based outcome predictor for ER+ and/or PR+ (i.e. Luminal) breast cancer patients using biological properties of the tumors. First, we identified estrogen-regulated genes using the ER+ MCF-7 breast cancer cell line treated with estrogen. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
4 related Platforms
174 Samples
Download data
Series
Accession:
GSE2740
ID:
200002740
5.

Gene Expression Preferentially Regulated by Tamoxifen in Breast Cancer Cells

(Submitter supplied) The beneficial effect of the selective estrogen receptor modulator (SERM) tamoxifen in the treatment and prevention of breast cancer is assumed to be through its ability to antagonize the stimulatory actions of estrogen, although tamoxifen can also have some estrogen-like agonist effects. Here we report that in addition to these mixed agonist/antagonist actions, tamoxifen can also selectively regulate a unique set of more than 60 genes in estrogen receptor alpha (ERa)-positive MCF-7 human breast cancer cells which are minimally regulated by estradiol or raloxifene. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2367
Platform:
GPL96
17 Samples
Download data
Series
Accession:
GSE4025
ID:
200004025
6.
Full record GDS2367

Tamoxifen effect on breast cancer cell line expressing estrogen receptor alpha and beta

Analysis of estrogen receptor alpha (ERalpha)-positive MCF-7 breast cancer (BC) cells infected with adenovirus-ERbeta and treated with tamoxifen (Tam). Tam is a selective ER modulator used in BC prevention and treatment. Results provide insight into Tam activity in the presence of both ERs.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 agent, 2 infection sets
Platform:
GPL96
Series:
GSE4025
17 Samples
Download data
DataSet
Accession:
GDS2367
ID:
2367
7.

A Modular Analysis of Breast Cancer Reveals a Novel Low-Grade Molecular Signature in Estrogen Receptor-Positive Tumors

(Submitter supplied) Primary human breast tumors were obtained from the National Cancer Centre of Singapore (NCC) Tissue Repository, after appropriate approvals from the NCC Repository and Ethics Committees. Profiled samples contained at least 50% tumor content. Keywords = Gene expression Keywords = Breast Cancer Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
96 Samples
Download data
Series
Accession:
GSE2294
ID:
200002294
8.

Estrogen effects on MCF-7 breast cancer cells co-expressing ERa and ERb

(Submitter supplied) Two subtypes of the estrogen receptor, ERalpha and ERbeta, mediate the actions of estrogens, and the majority of human breast tumors contain both ERalpha and ERbeta. To examine the possible interactions and modulatory effects of ERbeta on ERalpha activity, we have used adenoviral gene delivery to produce human breast cancer (MCF-7) cells expressing ERbeta, along with their endogenous ERalpha. We have examined the effects of ERβ expression on genome-wide gene expression by Affymetrix GeneChip microarrays. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2770
Platform:
GPL96
12 Samples
Download data
Series
Accession:
GSE4006
ID:
200004006
9.
Full record GDS2770

Estrogen effect on breast cancer cell line coexpressing estrogen receptors alpha and beta

Analysis of estrogen receptor (ER) alpha positive MCF-7 breast cancer cells following introduction of ERbeta and treatment with estrogen. The majority of breast cancers express both ERalpha and ERbeta. Results provide insight into the comodulatory effects of these two ERs.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 3 infection sets
Platform:
GPL96
Series:
GSE4006
12 Samples
Download data
DataSet
Accession:
GDS2770
ID:
2770
10.

The effect of miRNA overexpression on gene expression profile of MCF-7 cells

(Submitter supplied) To identify microRNAs impacting estrogen receptor ERα expression in breast cancer, we have screened ER-positive breast cancer cells with a library of pre-miRs, and systematically monitored the ERα expression by protein lysate microarrays. There was a significant enrichment of the in silico predicted ERα targeting microRNAs among the hits. The most potent pre-miRs miR-18a/b, miR-193b, miR-206, and miR-302c, were confirmed to directly target ERα and to repress estrogen-responsive genes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6102
11 Samples
Download data: TXT
Series
Accession:
GSE14847
ID:
200014847
11.

TFAP2C regulates multiple pathways of estrogen signaling

(Submitter supplied) We were interested in determining what genes might be controlled by TFAP2C and/or TFAP2A, either directly or indirectly through regulation of ER-alpha and potentially other signaling pathways. We performed an microarray analysis in MCF7 cells with elimination of either TFAP2C or TFAP2A. The patterns of gene expression with alteration of TFAP2 activity were compared to changes in expression induced by estrogen exposure. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE8640
ID:
200008640
12.

AP2 transcription factors regulate expression of CRABPII in hormone responsive breast carcinoma

(Submitter supplied) BACKGROUND: The AP2 transcription factor family is a set of developmentally regulated, retinoic acid (RA) inducible genes, which regulate expression of estrogen receptor-alpha (ERalpha) in breast carcinoma. We hypothesized that AP2 factors regulate a set of genes characteristic of the hormone responsive breast cancer phenotype. To better understand the role of AP2 factors in hormone responsive breast cancer, we sought to identify AP2-target genes in breast epithelial cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL2670 GPL3147
4 Samples
Download data
Series
Accession:
GSE7616
ID:
200007616
13.

Gene transcription signature of obesity in breast cancer

(Submitter supplied) Obesity is thought to contribute to worse disease outcome in breast cancer as a result of increased levels of adipocyte-secreted endocrine factors, insulin, and insulin-like growth factors (IGFs) that accelerate tumor cell proliferation and impair treatment response. We examined the effects of patient obesity on primary breast tumor gene expression, by profiling transcription of a set of tumors for which the patients’ body mass index (BMI) was ascertained. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
103 Samples
Download data: CEL
Series
Accession:
GSE24185
ID:
200024185
14.

[E-MTAB-345] ChIP-Seq of human MCF-7 cells with anti-ERalpha following estrogen treatment

(Submitter supplied) We performed chromatin immunoprecipitation (ChIP) with overnight with antibodies against the C-terminus (HC-20, from Santa Cruz Biotechnology, Europe) or the N-terminus (anti-Estrogen Receptor 18-32, from SigmaAldrich, Italy) of human ER-alpha with or without estrogen treatment for 45 minutes on TAP-ER-beta cells, and the immunoprecipitated DNA was sequenced with the Illumina/Solexa Genome Analyzer. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9115
8 Samples
Download data: TXT
Series
Accession:
GSE25769
ID:
200025769
15.

Breast Cancer Gene Expression Analysis

(Submitter supplied) Analysis of 104 breast cancer biopsies (removed prior to any treatment with tamoxifen or chemotherapeutic agents) from patients aged between 31 years and 89 years at the time of diagnosis (mean age = 58 years). Twenty were less than 50 years and seventy-seven women were 50 years, or older, at diagnosis. The size of the tumours ranged between 0.6 cm and 8.0 cm (mean = 2.79 cm). Eighteen tumours were T1 (<2 cm) in maximal dimension; 83 were T2 (2–5 cm) and 3 tumours were T3 (>5 cm). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
121 Samples
Download data: CEL
Series
Accession:
GSE42568
ID:
200042568
16.

The ERβ cistrome in colon cancer

(Submitter supplied) In order to elucidate the mechanism of ERβ in the colon, we validated ERβ antibodies, opti-mized chromatin-immunoprecipitation (ChIP), and performed ChIP-Seq of CRC engineered cell lines re-expressing ERβ.We present for the first time, the cistrome of nuclear receptor ERβ in different CRC cell lines.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21697
11 Samples
Download data: BEDGRAPH
Series
Accession:
GSE149979
ID:
200149979
17.

A genomic view of estrogen actions in human breast cancer cells

(Submitter supplied) Changes in the expression of 8400 genes were monitored by cDNA microarray analysis during the first 32 h of human breast cancer (BC) ZR-75.1 cell stimulation with a mitogenic dose of 17beta-estradiol, a timing which corresponds to completion of a full mitotic cycle in hormone-stimulated cells. Hierarchical clustering of 344 genes whose expression either increases or decreases significantly in response to estrogen reveals that the gene expression program activated by the hormone in these cells shows 8 main patterns of gene activation/inhibition. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL970
25 Samples
Download data
Series
Accession:
GSE1864
ID:
200001864
18.

Transcriptional characterization of a prospective series of primary plasma cell leukemia revealed genes associated with tumor progression and poorest outcome

(Submitter supplied) Plasma cell leukemia (PCL) is a rare form of plasma cell dyscrasia that presents either as a progression of previously diagnosed multiple myeloma (MM), namely secondary PCL (sPCL), or as the initial manifestation of disease, namely primary PCL (pPCL). Although presenting signs and symptoms include those seen in MM, pPCL is characterized by several aspects that clearly define more aggressive course. To provide insights into the biology of pPCL, we have investigated the transcriptional profiles of a cohort of 21 newly-diagnosed, homogeneously treated pPCL patients included in a multicenter prospective clinical trial. All but one pPCL had one of the main IGH translocations, whose associated transcriptional signatures resembled those observed in MM. A 503-gene signature was identified that distinguished pPCL from MM, from which emerged 28 genes whose trend in expression levels was found associated with the progressive stages of plasma cell dyscrasia in a large dataset of cases from multiple institutions, including samples from normal donors throughout PCL. The transcriptional pattern of the pPCL series was then evaluated in association with outcome. Three genes were identified having expression levels correlated with response to the first-line treatment with lenalidomide/dexamethasone, whereas a 27-gene signature was identified associated with overall survival independently of molecular alterations, hematological parameters and renal function. Overall, our data contribute to a fine dissection of pPCL and may provide novel insights into the molecular definition of a subgroup of high-risk pPCL.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
76 Samples
Download data: CEL
Series
Accession:
GSE39925
ID:
200039925
19.

Cell division cycle in a human cancer cell line (HeLa)

(Submitter supplied) This experiment set contains the complete set of raw data for Whitfield et al. (2002)Mol.Biol.Cell. HeLa S3 cells were synchronized by three different methods (double thymidine block, thymidine-nocodazole block or mitotic shake-off)in five independent time courses. mRNA from the first and second double thymidine block experiments were converted to cDNA by standard methods using an oligo-dT/random hexamer mix and hybridized to 24K arrays; mRNA from the third double thymidine and thymidine-nocodazole block experiments were converted to cDNA using olido-dT alone and hybridized to 43K arrays; total RNA from the mitotic shake-off experiment was first amplified using a modified eberwine protocol, aRNA converted to cDNA by reverse transcription with random hexamer and hybridized to 43K arrays. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
6 related Platforms
114 Samples
Download data
Series
Accession:
GSE3497
ID:
200003497
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