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Links from GEO DataSets

Items: 20

1.

Expression data from age-dichotomized ER+ breast tumors

(Submitter supplied) To investigate the biological basis between aging and sporadic breast cancer incidence and prognosis, RNA samples from matched ER+ invasive breast cancers diagnosed in either young (≤45) or old (≥70) women were analyzed by expression microarrays Keywords: biomarker identification
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4685
47 Samples
Download data: CEL
Series
Accession:
GSE8193
ID:
200008193
2.

Expression data of MCF7 cells following short-term E deprivation, ER-alpha siRNA knockdown and oxidant treatments

(Submitter supplied) To investigate the oxidant sensitivity of E/ER regulated gene expression, E/ER regulated genes are identified using E deprivation or ER-alpha siRNA knockdown; and oxidative stress responsive is determined by 8hr exposure to diamide, hydrogen peroxide and menadione Keywords: biomarker identification
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL3921
12 Samples
Download data: CEL
Series
Accession:
GSE10061
ID:
200010061
3.

aCGH data from age-dichotomized ER+ breast tumors

(Submitter supplied) To investigate the biological basis between aging and sporadic breast cancer incidence and prognosis, DNA samples from matched ER+ invasive breast cancers diagnosed in either young (<45) or old (>70) women were analyzed with aCGH Keywords: biomarker identification
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL4999
71 Samples
Download data: XLS
Series
Accession:
GSE8801
ID:
200008801
4.

Expression data from age-dichotomized ER+, N0 breast tumors

(Submitter supplied) Signaling pathways that converge on two different transcription factor complexes, NFκB and AP-1, have been identified in estrogen receptor (ER)-positive breast cancers resistant to the antiestrogen, tamoxifen. In this study, biomarkers co-ordinately up-regulated by NFKB and AP-1 with prognositic significance are identified in a largely TAM-treated set of ER+ node negative breast cancers. The prognostic value with respect to age is also investigated. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4685
54 Samples
Download data: CEL
Series
Accession:
GSE7378
ID:
200007378
5.

Expression data from MCF7 and BT474 cell lines after long term estrogen deprivation culture

(Submitter supplied) MCF7 and BT474 cell lines were exposed to LTED culture for 0 and 2 days, 6 weeks and 10 months and monitored for changes in gene expression
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE50820
ID:
200050820
6.

Genomic predictor of response and survival following neoadjuvant taxane-anthracycline chemotherapy in breast cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
508 Samples
Download data: CEL, TXT
Series
Accession:
GSE25066
ID:
200025066
7.

Gene expression profiling of the 20 human early breast carcinomas by three miaroarray platforms

(Submitter supplied) In this study, we profiled gene expressions on 20 biopsy tissues of early stage breast carcinoma using Applied Biosystem’s Human Genome Survey Microarrays. Two main previously defined clinically relevant subtypes of breast tumors, Luminal A (longest survival time) and Basal (shortest survival time) were identified. Statistical analysis identified 1210 genes as signature genes characterizing the two subtypes of breast cancer. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL1843 GPL1708 GPL1426
80 Samples
Download data
Series
Accession:
GSE3155
ID:
200003155
8.

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
9.

Cholesterol biosynthesis pathway as a novel mechanism of resistance to estrogen deprivation in estrogen receptor positive breast cancer

(Submitter supplied) Therapies targeting estrogenic stimulation in estrogen receptor positive (ER+) breast cancer (BC) reduce mortality, but resistance remains a major clinical problem. Molecular studies have shown few high frequency mutations to be associated with endocrine resistance. In contrast, expression profiling of primary ER+ BC samples has identified several promising signatures/networks for targeting. In this study, the cholesterol biosynthesis pathway was the common upregulated pathway in the ER+ LTED but not ER- LTED cell lines, suggesting a potential mechanism dependent on continued ER expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
54 Samples
Download data: TXT
Series
Accession:
GSE75971
ID:
200075971
10.

Posttranslationally modified progesterone receptors direct ligand-specific expression of breast cancer stem cell-associated gene programs

(Submitter supplied) Background Estrogen and progesterone are potent breast mitogens. In addition to steroid hormones, multiple signaling pathways input to estrogen receptor (ER) and progesterone receptor (PR) actions via posttranslational events. Protein kinases commonly activated in breast cancers phosphorylate steroid hormone receptors (SRs) and profoundly impact their activities. Methods To better understand the role of modified PRs in breast cancer, we measured total and phospho-Ser294 PRs in 209 human breast tumors represented on 2754 individual tissue spots within a tissue microarray and assayed the regulation of this site in human tumor explants cultured ex vivo. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
84 Samples
Download data: TXT
Series
Accession:
GSE94363
ID:
200094363
11.

Genomic agonism and phenotypic antagonism between estrogen and progesterone receptors in breast cancer. [ChIP-seq]

(Submitter supplied) Transcriptomic changes and estrogen and progesterone receptor binding in multiple ER+/PR+ models (eight ER+/PR+ patient tumors, various T47Ds, ZR75) and multiple ER+/PR-negative models (four ER+/PR- patient tuumors, PR-deficient T47D and MCF7 cells) treated with various hormone combinations. Results: In isolation, estrogen and progestin act as genomic agonists by regulating the expression of common target genes in similar directions, but at different levels. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
26 Samples
Download data: BED
Series
Accession:
GSE80367
ID:
200080367
12.

Genomic agonism and phenotypic antagonism between estrogen and progesterone receptors in breast cancer. [cell models RNA-seq]

(Submitter supplied) Transcriptomic changes and estrogen and progesterone receptor binding in multiple ER+/PR+ models (eight ER+/PR+ patient tumors, various T47Ds, ZR75) and multiple ER+/PR-negative models (four ER+/PR- patient tuumors, PR-deficient T47D and MCF7 cells) treated with various hormone combinations. Results: In isolation, estrogen and progestin act as genomic agonists by regulating the expression of common target genes in similar directions, but at different levels. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
28 Samples
Download data: CSV
Series
Accession:
GSE80366
ID:
200080366
13.

Genomic agonism and phenotypic antagonism between estrogen and progesterone receptors in breast cancer. [tumor samples RNA-seq]

(Submitter supplied) Transcriptomic changes and estrogen and progesterone receptor binding in multiple ER+/PR+ models (eight ER+/PR+ patient tumors, various T47Ds, ZR75) and multiple ER+/PR-negative models (four ER+/PR- patient tuumors, PR-deficient T47D and MCF7 cells) treated with various hormone combinations. Results: In isolation, estrogen and progestin act as genomic agonists by regulating the expression of common target genes in similar directions, but at different levels. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
48 Samples
Download data: CSV
Series
Accession:
GSE80365
ID:
200080365
14.

Genomic agonism and phenotypic antagonism between estrogen and progesterone receptors in breast cancer.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
102 Samples
Download data
Series
Accession:
GSE80098
ID:
200080098
15.

Identification of subtypes in HER2-positive breast cancer reveals a gene signature prognostic of outcome

(Submitter supplied) Purpose HER2 gene amplification or protein overexpression (HER2+) defines a clinically challenging subgroup of breast cancer with variable prognosis and response to therapy. We aimed to investigate the heterogeneous biological appearance and clinical behavior of HER2+ tumors using molecular profiling. Materials and Methods Hierarchical clustering of gene expression data from 58 HER2-amplified tumors of various stage, histological grade and estrogen receptor (ER) status was used to construct a HER2-derived prognostic predictor that was further evaluated in several large independent breast cancer data sets. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5345
58 Samples
Download data: GPR, TXT
Series
Accession:
GSE18328
ID:
200018328
16.

Estrogen and progesterone receptor dynamics in patient-derived luminal breast cancer xenografts

(Submitter supplied) Progesterone receptors (PR) are co-expressed in over half of estrogen receptor (ER) positive breast cancers and predict positive response to endocrine therapy. PR can directly and globally modify ER action to attenuate tumor growth. However, whether this suppression occurs solely through PR-ER interactions remains unknown. We assessed tumor growth in two highly ER and PR positive breast cancer patient-derived xenografts (PDX) and found that natural and synthetic progestins potently antagonize the mitogenic effects of estrogens. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL11532
12 Samples
Download data: CEL
Series
Accession:
GSE93944
ID:
200093944
17.

ChIPseq analysis of patient-derived luminal breast cancer xenografts with progestins

(Submitter supplied) Primary breast cancer xenografts
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
24 Samples
Download data: BED
Series
Accession:
GSE93108
ID:
200093108
18.

RNAseq analysis of patient-derived luminal breast cancer xenografts treated with progestins

(Submitter supplied) Primary breast cancer xenografts
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: FPKM_TRACKING
19.

High-resolution aCGH analyses of copy number alterations in HER2-amplified breast cancer

(Submitter supplied) HER2 gene amplification and protein overexpression (HER2+) define a clinically challenging subgroup of breast cancer with variable prognosis and response to therapy. Although gene expression profiling has identified an ERBB2 molecular subtype of breast cancer, it is clear that HER2+ tumors reside in all molecular subtypes and represent a genomically and biologically heterogeneous group. Genome-wide DNA copy number profiling, using BAC array comparative genomic hybridization (aCGH) were performed on 200 tumors with mixed clinical characteristics and amplification of HER2. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platforms:
GPL9077 GPL7247 GPL4723
200 Samples
Download data: GPR
Series
Accession:
GSE21259
ID:
200021259
20.

Gene profile of breast cancers with immunohistochemical phenotypes of ER+/- and/or HER2+/-

(Submitter supplied) Hormones and growth factors accelerate cell proliferation of breast cancer cells, and these molecules are well investigated targets for drug development and application. The mechanisms of cell proliferation of breast cancers lacking estrogen receptor (ER) and HER2 have not been fully understood. The purpose of the present study is to find genes that are differentially expressed in breast cancers and that might significantly contribute to cell proliferation in these cancers. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8300
40 Samples
Download data: CEL, XLSX
Series
Accession:
GSE6367
ID:
200006367
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