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Links from GEO DataSets

Items: 20

1.

Letrozole-, Anastrozole- and Tamoxifen-Responsive Genes in MCF-7aro Cells

(Submitter supplied) Anti-estrogens and aromatase inhibitors are important drugs in the treatment of estrogen-dependent breast cancer. In order to investigate the effects of these drugs on gene expression in breast cancer cells, we treated estrogen receptor-positive MCF-7 cells, stably transfected with the aromatase gene (known as MCF-7aro cells), with testosterone, 17β-estradiol, two aromatase inhibitors (letrozole and anastrozole), and an anti-estrogen (tamoxifen). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1873
Platform:
GPL96
18 Samples
Download data: CEL, EXP
Series
Accession:
GSE2225
ID:
200002225
2.
Full record GDS1873

Antiestrogen and aromatase inhibitor effect on breast cancer cells

Analysis of estrogen receptor positive, aromatase transfected MCF-7 cells after treatment with an antiestrogen (AE) or an aromatase inhibitor (AI). AEs and AIs are used to treat estrogen-dependent breast cancer. Cells also treated with androgen which is converted to estrogen by aromatase.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 6 agent, 4 other sets
Platform:
GPL96
Series:
GSE2225
18 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS1873
ID:
1873
3.

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
4.
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
5.

The expression patterns of 17b-estradiol responsive genes in wt MCF7, OHT resistant MCF7 and ICI resistant MCF7

(Submitter supplied) Compare the expression pattern of 17b-estradiol responsive genes in parent, OHT-resistant and ICI-resistant breast cancer cells. Keywords: 17b-estradiol responsive genes, OHT resistance, Fulvestrand resistance
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
24 Samples
Download data
Series
Accession:
GSE5840
ID:
200005840
6.

microRNA expression profiles in Aromatase Inhibitor-Resistant, Tamoxifen-Resistant and LTED breast cancer cell lines.

(Submitter supplied) Resistance to endocrine therapy agents has presented a clinical obstacle in the treatment of hormone-dependent breast cancer. Our laboratory has initiated a study of microRNA regulation of signaling pathways that may result in breast cancer progression on aromatase inhibitors (AI). Microarray analysis of microRNA expression identified 115 significantly regulated microRNAs, of which 49 microRNAs were believed to be hormone-responsive. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL9081
23 Samples
Download data: TXT
Series
Accession:
GSE17775
ID:
200017775
7.

Hyperactivation of PI3K promotes escape from hormone dependence in estrogen receptor-positive breast cancer

(Submitter supplied) Hyperactivation of phosphatidylinositol-3 kinase (PI3K) promotes escape from hormone dependence in estrogen receptor-positive breast cancer. A significant fraction of breast cancers exhibit de novo or acquired resistance to estrogen deprivation. We used gene expression microarrays to identify genes and pathways that are commonly dysregulated in ER+ cell lines with acquired hormone-independent growth. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
24 Samples
Download data: CEL, CHP
Series
Accession:
GSE19639
ID:
200019639
8.

Expression data from MCF-7aro aromatase inhibitor-resistant, tamoxifen-resistant and LTEDaro lines.

(Submitter supplied) MCF-7aro cells were used to generate a cell culture model system that is resistant to 3 aromatase inhibitors (AIs), letrozole, anastrozole and exemestane. For comparison, the MCF-7aro cells were also used to generate the tamoxifen-resistant cells as well as long-term estrogen deprived, LTEDaro. Affymetrix microarray analysis was performed to determine changes in gene expression that are unique to AI-resistance. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
42 Samples
Download data: CEL
Series
Accession:
GSE10911
ID:
200010911
9.

Gene profiling and prediction of response to anastrozole neoadjuvant treatment in breast cancer

(Submitter supplied) Transcriptome of 17 tru-cut biopsies and 13 matched surgical samples from ER+ breast tumor patients, treated for 3 months with Anastrozole were anayzed to identify a robust expression signature predictive of response to Anastrozole neoadjuvant treatment in ER+ breast cancer patients and, at the same time, to delineate treatment effects.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL6480 GPL6848
60 Samples
Download data: TXT
Series
Accession:
GSE18378
ID:
200018378
10.

Comparison of tamoxifen and letrozole response in mammary preneoplasia of ER and aromatase over-expressing mice defines an immune-associated gene signature linked to tamoxifen resistance

(Submitter supplied) To investigate response or resistance to endocrine therapy, mice with targeted over-expression of Esr1 or CYP19A1 to mammary epithelial cells were employed, representing two direct pathophysiological interventions in estrogen pathway signaling. Both Esr1 and CYP19A1 over-expressing mice responded to letrozole with reduced HAN prevalence and decreased mammary epithelial cell proliferation. CYP19A1 over-expressing mice were tamoxifen-sensitive but Esr1 over-expressing mice were tamoxifen-resistant. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
17 Samples
Download data: TXT
Series
Accession:
GSE63857
ID:
200063857
11.

Letrozole (Femara) early and late responses to treatment

(Submitter supplied) In the present investigation, we have exploited the opportunity provided by neoadjuvant treatment of a group of postmenopausal women with large operable or locally advanced breast cancer (in which therapy is given with the primary tumour remaining within the breast) to take sequential biopsies of the same cancers before and after 10-14 days or 90 days treatment with letrozole. RNA extracted from the biopsies has been subjected to Affymetrix microarray analysis and the data from paired biopsies interrogated to discover genes whose expression is most influenced by oestrogen deprivation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
176 Samples
Download data: CEL
Series
Accession:
GSE20181
ID:
200020181
12.

27_RA_RMA_Jan04_time_course

(Submitter supplied) This series represents murine dorsal neural tube bisected along the midline with one half from each embryo used for control and the other half treated with 10-6M RA dissolved in ethanol for 6, 12, 24 or 48 h. For 6 h exposures, the explants were cultured overnight on fibronectin coated 35mm dishes (Biocoat, Becton Dickinson Labware, Bedford, MA) in DMEM with 10% horse serum in order to allow for sufficient outgrowth of neural crest cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS773
Platform:
GPL81
27 Samples
Download data: CEL, EXP
Series
Accession:
GSE1588
ID:
200001588
13.
Full record GDS773

Retinoic acid teratogenic effect on cranial neural crest: time course

Expression profiling of cranial neural crest exposed to 1 uM retinoic acid (RA) at various lengths of time up to 48 hours. Neural crest obtained from 8.5 days postcoitum ICR embryos. Results provide insight into developmental pathways affected upon exposure to teratogenic concentrations of RA.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 agent, 4 time sets
Platform:
GPL81
Series:
GSE1588
27 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS773
ID:
773
14.

Cell-type specific responses to chemotherapeutics in breast cancer

(Submitter supplied) Recent studies have identified clinical subtypes of breast tumors that arise from different cell types and have different outcomes in response to chemotherapy. Tumors derived from basal epithelium have a poorer prognosis than tumors derived from luminal epithelium. To gain insight into differences underlying this disparity, we treated cell lines derived from basal epithelium (immortalized human mammary epithelial cells) and those derived from luminal epithelium (MCF-7 and ZR-75-1) with two chemotherapeutics commonly used in the treatment of breast cancer. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS845 GDS846 GDS847 GDS848
Platform:
GPL550
75 Samples
Download data
Series
Accession:
GSE763
ID:
200000763
15.
Full record GDS848

Breast cancer cell line ZR-75-1 response to chemotherapeutics: time course

Analysis of the response of luminal epithelium derived breast cancer line ZR-75-1 to either doxorubicin or 5-fluorouracil. Cells examined 12, 24, and 36 hours following treatment. Results provide insight into the response of breast cancers derived from different cell types to chemotherapeutics.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent, 3 time sets
Platform:
GPL550
Series:
GSE763
19 Samples
Download data
DataSet
Accession:
GDS848
ID:
848
16.
Full record GDS847

Breast cancer cell line MCF-7 response to chemotherapeutics: time course

Analysis of the response of luminal epithelium derived breast cancer line MCF-7 to either doxorubicin or 5-fluorouracil. Cells examined 12, 24, and 36 hours following treatment. Results provide insight into the response of breast cancers derived from different cell types to chemotherapeutics.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent, 3 time sets
Platform:
GPL550
Series:
GSE763
19 Samples
Download data
DataSet
Accession:
GDS847
ID:
847
17.
Full record GDS846

Breast cancer cell line HME-CC response to chemotherapeutics: time course

Analysis of the response of basal epithelium derived breast cancer line HME-CC to either doxorubicin or 5-fluorouracil. Cells examined 12, 24, and 36 hours following treatment. Results provide insight into the response of breast cancers derived from different cell types to chemotherapeutics.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent, 3 time sets
Platform:
GPL550
Series:
GSE763
19 Samples
Download data
DataSet
Accession:
GDS846
ID:
846
18.
Full record GDS845

Breast cancer cell line ME16C response to chemotherapeutics: time course

Analysis of the response of the basal epithelium derived breast cancer line ME16C to either doxorubicin or 5-fluorouracil. Cells examined 12, 24, and 36 hours following treatment. Results provide insight into the response of breast cancers derived from different cell types to chemotherapeutics.
Organism:
Homo sapiens
Type:
Expression profiling by array, log ratio, 3 agent, 3 time sets
Platform:
GPL550
Series:
GSE763
18 Samples
Download data
DataSet
Accession:
GDS845
ID:
845
19.

Letrozole (Femara) early response to treatment

(Submitter supplied) In the present investigation, we have exploited the opportunity provided by neoadjuvant treatment of a group of postmenopausal women with large operable or locally advanced breast cancer (in which therapy is given with the primary tumour remaining within the breast) to take sequential biopsies of the same cancers before and after 10-14 days treatment with letrozole. RNA extracted from the biopsies has been subjected to Affymetrix microarray analysis and the data from paired biopsies interrogated to discover genes whose expression is most influenced by oestrogen deprivation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3116
Platform:
GPL96
116 Samples
Download data: CEL
Series
Accession:
GSE5462
ID:
200005462
20.
Full record GDS3116

Letrozole effect on breast cancer tumors

Analysis of breast cancer tumors following treatment with letrozole for 14 days. The aromatase inhibitor letrozole is an anti-estrogen drug used to treat postmenopausal women with breast cancer. Results provide insight into the molecular mechanism of action of letrozole in breast cancer.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 58 individual sets
Platform:
GPL96
Series:
GSE5462
116 Samples
Download data: CEL
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