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Links from GEO DataSets

Items: 20

1.

Anti-prolif. effect of E2 in breast cancer cells that re-exp. ERalpha is mediated by aberr. regulat. of cell cycle genes

(Submitter supplied) Gene expression changes caused by estrogen treatment of breast cancer cells that re-express ERalpha was investigated by infecting ER-negative MDA-MB-231 breast cancer cells for 24 h with recombinant adenovirus encoding full-length human ERalpha (Ad-ERalpha) or control vector (Ad-LacZ), and treating them with 0·01% ethanol (vehicle control) or 10-8 M 17beta-estradiol (E2). After 48 h of treatment, total RNA was isolated and used for transcript profiling on Affymetrix GeneChips. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1326
Platform:
GPL96
12 Samples
Download data
Series
Accession:
GSE2251
ID:
200002251
2.
Full record GDS1326

Breast cancer cells reexpressing estrogen receptor alpha response to 17beta-estradiol

Analysis of the response of estrogen receptor (ER) negative MDA-MB-231 breast cancer cells infected with full-length ER alpha adenoviral constructs to treatment with 17beta-estradiol (E2). Results provide insight into the anti-proliferative effect of E2 on breast cancer cells reexpressing ER.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 2 protocol sets
Platform:
GPL96
Series:
GSE2251
12 Samples
Download data
DataSet
Accession:
GDS1326
ID:
1326
3.

Profiling of three different ER+ breast cancer cell lines grown in the presence and absence of estrogen.

(Submitter supplied) Three human ER+ breast cancer cell lines--MCF-7, T47-D, BT-474--grown with or without estradiol (E2). Keywords: Cell Line Comparison
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1549
Platform:
GPL96
12 Samples
Download data: CEL
Series
Accession:
GSE3529
ID:
200003529
4.
Full record GDS1549

Estrogen effect on estrogen receptor alpha positive breast cancer cell lines

Expression profiling of estrogen receptor positive breast cancer cell lines treated with estradiol for 24 hours. MCF-7, T47-D, and BT-474 breast cancer cell lines examined. Results identify candidate genes involved in estrogen stimulated breast cancer growth.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 3 cell line sets
Platform:
GPL96
Series:
GSE3529
12 Samples
Download data: CEL
DataSet
Accession:
GDS1549
ID:
1549
5.

Estrogen regulation and physiopathologic significance of alternative promoters in breast cancer

(Submitter supplied) Alternative promoters (APs) occur in >30% protein-coding genes and contribute to proteome diversity. However, large-scale analyses of AP regulation are lacking, and little is known about their potential physiopathologic significance. To better understand the transcriptomic impact of estrogens, which play a major role in breast cancer, we analyzed gene and AP regulation by estradiol in MCF7 cells using pan-genomic exon arrays. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL5188 GPL5175
32 Samples
Download data: CEL
Series
Accession:
GSE20342
ID:
200020342
6.

Effects of estrogen

(Submitter supplied) Effects of estrogen on global gene expression: identification of novel targets of estrogen action. Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by SAGE
Platform:
GPL4
4 Samples
Download data
Series
Accession:
GSE41
ID:
200000041
7.

Novel Estrogen Receptor-{alpha} Binding Sites and Estradiol Target Genes Identified by ChIP Cloning in Breast Cancer.

(Submitter supplied) Estrogen receptor-{alpha} (ER{alpha}) and its ligand estradiol play critical roles in breast cancer growth and are important therapeutic targets for this disease. Using chromatin immunoprecipitation (ChIP)-on-chip, ligand-bound ER{alpha} was recently found to function as a master transcriptional regulator via binding to many cis-acting sites genome-wide. Here, we used an alternative technology (ChIP cloning) and identified 94 ER{alpha} target loci in breast cancer cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3283
Platform:
GPL570
9 Samples
Download data: CEL
Series
Accession:
GSE11506
ID:
200011506
8.
Full record GDS3283

Estradiol effect on breast cancer cell line: time course

Analysis of MCF-7 breast cancer cells treated with estradiol for 3 or 6 hours. Results combined with ChIP experiments to identify estrogen receptor alpha binding sites and estradiol target genes in breast cancer cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 2 time sets
Platform:
GPL570
Series:
GSE11506
9 Samples
Download data: CEL
DataSet
Accession:
GDS3283
ID:
3283
9.

Profiling of MCF-7 cell lines stably overexpressing (ca)Raf-1, (ca)MEK, (ca)erbB-2, or ligand-activatable EGFR.

(Submitter supplied) Profiling of MCF-7 cell lines stably overexpressing constitutively active Raf-1, constitutively active MEK, constitutively active c-erbB-2, or ligand-activatable EGFR as models of overexpressed growth factor signaling, as well as control vector transfected cells (coMCF-7) and control vector transfected cells long-term adapted for estrogen-independent growth (coMCF-7/lt-E2). Keywords: Cell Line Comparison
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1925
Platform:
GPL96
18 Samples
Download data: CEL
Series
Accession:
GSE3542
ID:
200003542
10.
Full record GDS1925

Estrogen receptor alpha positive breast cancer cells response to hyperactivation of MAPK pathway

Analysis of estrogen receptor (ER) alpha positive MCF-7 breast cancer cells overexpressing constitutively active Raf-1, constitutively active MEK, constitutively active c-erbB-2, or ligand-activatable EGFR. Results indicate that increased MAPK activation results in loss of ER-alpha expression.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 6 cell line sets
Platform:
GPL96
Series:
GSE3542
18 Samples
Download data: CEL
DataSet
Accession:
GDS1925
ID:
1925
11.

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
12.
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
13.

Gene Regulation by Estrogen Signaling and DNA Methylation in MCF7 Breast Cancer Cells

(Submitter supplied) Estrogen signaling and epigenetic modifications, in particular DNA methylation, are involved in regulation of gene expression in breast cancers. Here we investigated a potential regulatory cross-talk between these two pathways by identifying their common target genes and exploring potential underlying molecular mechanisms in human MCF7 breast cancer cells. Principal Findings: Gene expression profiling revealed that the expression of approximately 150 genes was influenced by both 17β-estradiol (E2) and a hypomethylating agent 5-aza-2’-deoxycytidine (DAC). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
12 Samples
Download data: CEL, XLS
Series
Accession:
GSE36683
ID:
200036683
14.

An estrogen-dependent model of breast cancer created by transformation of normal human mammary epithelial cells

(Submitter supplied) This study was performed to check that ESR1 and BMI1 are biologically active after lentiviral transduction of primary human mammary epithelial cells (HMECs) with lentiviral vectors expressing ESR1 and BMI1 from the human PGK promoter. ESR1 targets like PGR, PRLR and GREB1, but not TFF1 and XBP1, were induced by estradiol in the ESR1-expressing cells. BMI1 targets like BMI1, NEFL and CCND2 were repressed in the BMI1-expressing cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE6548
ID:
200006548
15.

Overlapping and distinct functions between ERα and ERβ homodimers and corresponding transcriptomes in the same cellular context

(Submitter supplied) The two estrogen receptors, ERα and ERβ function as ligand-inducible transcription factors. Most in vitro studies have reported that ERα drives breast cancer growth whereas ERβ, if expressed, suppresses growth. To dissect function and gene expression profile regulated by ERα or ERβ, respectively, we generated a novel cell model expressing only ERβ, by applying CRISPR-cas9 to delete ERα in MCF7 cells with stable Tet-Off-inducible ERβ expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21697
12 Samples
Download data: XLSX
16.

Genomic analyses of breast cancer cells: 17β-hydroxysteroid dehydrogenase type 1 induces transcriptional changes in estradiol-dependent and independent manners

(Submitter supplied) 17β-HSD1 expression modulates T47D transcript profile in in steroid-deprived medium. The enzyme specifically regulates apoptosis and cancer-related genes in T47D cells cultured in steroid-deprived medium. Genes that primarily involved in Cell cycle progression, such as the Cyclin A2 gene, CCNA2, are generally down-regulated whereas most genes involved in apoptosis and cell death, such as the proapoptotic gene XAF1 and FGF12, are on the contrary up-regulated by 17β-HSD1 knockdown, and 21% of the modulated genes belong to this latter functional category. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
8 Samples
Download data: CEL
Series
Accession:
GSE77345
ID:
200077345
17.

Time-course effect of estradiol and estradiol-BSA on early gene expression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
38 Samples
Download data: CEL
Series
Accession:
GSE32670
ID:
200032670
18.

Time-course effect of estradiol and estradiol-BSA on early gene expression in SKBR3 cells

(Submitter supplied) Estrogens have been reported to activate several processes via membrane binding to either classic estrogen receptors (ERs) or GPR30. We have used either estradiol or BSA-conjugated estradiol in order to initiate membrane-initiated actions and ICI 172,780 (ICI) or G15 to explore ER- and GPR30-related transcription. Our results show that the majority of G15-inhibited transcription is depending on ERs, as it is also inhibited by ICI. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE32669
ID:
200032669
19.

Time-course effect of estradiol and estradiol-BSA on early gene expression in MDA-MB-231 cells

(Submitter supplied) Estrogens have been reported to activate several processes via membrane binding to either classic estrogen receptors (ERs) or GPR30. We have used either estradiol or BSA-conjugated estradiol in order to initiate membrane-initiated actions and ICI 172,780 (ICI) or G15 to explore ER- and GPR30-related transcription. Our results show that the majority of G15-inhibited transcription is depending on ERs, as it is also inhibited by ICI. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
11 Samples
Download data: CEL
Series
Accession:
GSE32668
ID:
200032668
20.

Time-course effect of estradiol and estradiol-BSA on early gene expression in MCF-7 cells

(Submitter supplied) Estrogens have been reported to activate several processes via membrane binding to either classic estrogen receptors (ERs) or GPR30. We have used either estradiol or BSA-conjugated estradiol in order to initiate membrane-initiated actions and ICI 172,780 (ICI) or G15 to explore ER- and GPR30-related transcription. Our results show that the majority of G15-inhibited transcription is depending on ERs, as it is also inhibited by ICI. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE32667
ID:
200032667
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