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Links from GEO DataSets

Items: 20

1.

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
2.

Validation cohort for genomic predictor of response and survival following neoadjuvant taxane-anthracycline chemotherapy in breast cancer

(Submitter supplied) PURPOSE: To develop a predictive test for response and survival following neoadjuvant taxane-anthracycline chemotherapy for HER2-negative invasive breast cancer. METHODS: We developed a microarray-based gene expression test from pre-treatment tumor biopsies (310 patients) to predict favorable outcome based on estrogen receptor (ER) status,pathologic response to chemotherapy, 3-year disease outcomes, and sensitivity to endocrine therapy. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
198 Samples
Download data: CEL
Series
Accession:
GSE25065
ID:
200025065
3.

Discovery cohort for genomic predictor of response and survival following neoadjuvant taxane-anthracycline chemotherapy in breast cancer

(Submitter supplied) PURPOSE: To develop a predictive test for response and survival following neoadjuvant taxane-anthracycline chemotherapy for HER2-negative invasive breast cancer. METHODS: We developed a microarray-based gene expression test from pre-treatment tumor biopsies (310 patients) to predict favorable outcome based on estrogen receptor (ER) status,pathologic response to chemotherapy, 3-year disease outcomes, and sensitivity to endocrine therapy. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
310 Samples
Download data: CEL
Series
Accession:
GSE25055
ID:
200025055
4.

Prediction of breast cancer pathological complete response to anthracycline/taxane chemotherapy.

(Submitter supplied) EORTC 10994 phase III breast cancer clinical trial comparing FEC (5-fluorouracil, cyclophosphamide, epirubicin) with ET (epirubicin, docetaxel). 161 needle biopsies of locally advanced or large operable breast tumours were hybridised to Affymetrix X3P chips. The array data from the ER negative tumours (28/65 pathological CR in the FEC arm, 27/59 pathological CR in the ET arm) were used to validate the cell line-based chemotherapy response predictors developed by the Potti/Nevins group at Duke University (doi:10.1038/nm1491). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1352
161 Samples
Download data: CEL
Series
Accession:
GSE6861
ID:
200006861
5.

IPH-926 human lobular breast cancer cells

(Submitter supplied) IPH-926 is an anticancer drug-resistant tumor cell line derived from a chemo-refractory human infiltrating lobular breast cancer (ILBC). IPH-926 ILBC cells were subjected to gene expression profiling using an Affymetrix HG U133 Plus 2.0 array.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
1 Sample
Download data: CEL
Series
Accession:
GSE28089
ID:
200028089
6.

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
7.

Transcriptome analysis of ER+/PR+, ER-/PR+ and triple negative breast tumors

(Submitter supplied) The goal of this study is to analyse whether ER-/PR+ breast tumors could be transcriptionally different from ER+/PR+ and/or from triple negative breast tumors
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21697
77 Samples
Download data: XLSX
Series
Accession:
GSE162332
ID:
200162332
8.

Endocrine Sensitivity Index Validation Dataset

(Submitter supplied) Validation dataset of 298 ER-positive patients treated with tamoxifen for 5 years. All patients in this dataset have ER+ breast cancer and were uniformly treated with tamoxifen for 5 years. The objective of the study was to correlate levels of genomic markers to outcomes (relapse free survival) in this cohort of uniformly treated patients.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
298 Samples
Download data: CEL
Series
Accession:
GSE17705
ID:
200017705
9.

Factorial study for evaluating the effect of Affy platform and lab on gene expression measurements

(Submitter supplied) Comparison of concordance in single and multi-gene genomic indices from data generated by two different laboratories (MD Anderson Cancer Center (MDA) and Jules Bordet Institute (JBI)) and on two different Affymetrix platforms (U113A and U133_Plus2). We used a 2x2 factorial study in which 16 clinical breast cancer samples were profiled by both laboratories on both platforms (64 arrays total).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL96 GPL570
64 Samples
Download data: CEL
Series
Accession:
GSE17700
ID:
200017700
10.

Expression data from breast cancer FNA biopsies from patients (US samples)

(Submitter supplied) This is Phase II Trial of 4courses of 5-fluorouracil, doxorubicin and cyclophosphamide follwed by 4 additional courses of weekly docetaxel and capecitabine administered as Preoperative Therapy for Patients with Locally Advanced Breast Cancer, Stages II and III by US oncology (PROTOCOL 02-103) We performed gene set analysis (GSA) using functionally annotated gene sets corresponding to almost all known biological processes in ER-positive/HER2negative and ER-negative/HER2-negative breast cancer, respectively.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4056
Platform:
GPL96
61 Samples
Download data: CEL
Series
Accession:
GSE23988
ID:
200023988
11.

Expression data from breast cancer FNA biopsies from patients

(Submitter supplied) We assess if distinct biological processes might be associated with chemotherapy sensitivity in the different clinical subsets of breast cancers. We performed gene set analysis (GSA) using functionally annotated gene sets corresponding to almost all known biological processes in ER-positive/HER2negative and ER-negative/HER2-negative breast cancer, respectively.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4057
Platform:
GPL96
103 Samples
Download data: CEL
Series
Accession:
GSE22093
ID:
200022093
12.
Full record GDS4057

ER-positive/HER2-negative and ER-negative/HER2-negative breast cancer biopsies (MDACC/IGR cohort)

Analysis of pre-treatment biopsies from 103 HER2-normal breast cancer patients (ER-positive and ER-negative subtypes) from MD Anderson Cancer Center/Institut Goustave Russy. Results provide insight into molecular mechanisms associated with chemotherapy sensitivity in breast cancer subtypes.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 6 disease state, 3 genotype/variation, 3 other, 4 specimen sets
Platform:
GPL96
Series:
GSE22093
103 Samples
Download data: CEL
13.
Full record GDS4056

ER-positive/HER2-negative and ER-negative/HER2-negative breast cancer biopsies (USO-02103 cohort)

Analysis of pre-treatment biopsies from 62 HER2-normal breast cancer patients (ER-positive and ER-negative subtypes) from US Oncology clinical trial 02103. Results provide insight into molecular mechanisms associated with chemotherapy sensitivity in breast cancer subtypes.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 3 disease state, 2 genotype/variation, 2 other, 4 specimen sets
Platform:
GPL96
Series:
GSE23988
61 Samples
Download data: CEL
DataSet
Accession:
GDS4056
ID:
4056
14.

Expression data from breast cancer FNA biopsies from patients ( (USO samples)

(Submitter supplied) Tumor samples were obtained from patients with stage II-III breast cancer before starting neoadjuvant chemotherapy with four cycles of 5-fluorouracil/epirubicin/cyclophosphamide (FEC) followed by four cycles of docetaxel/capecitabine (TX) on US Oncology clinical trial 02-103. Most patients with HER-2-positive cancer also received trastuzumab (H).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
91 Samples
Download data: CEL
Series
Accession:
GSE42822
ID:
200042822
15.

Multifactorial Approach to Predicting Resistance to Anthracyclines

(Submitter supplied) PURPOSE: Validated biomarkers predictive of response/resistance to anthracyclines in breast cancer are currently lacking. The neoadjuvant TOP trial, in which patients with estrogen receptor (ER)-negative tumors were treated with anthracycline (epirubicin) monotherapy, was specifically designed to evaluate the predictive value of topoisomerase IIα (TOP2A) and to develop a gene expression signature to identify those patients who do not benefit from anthracyclines. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
120 Samples
Download data: CEL, TXT
Series
Accession:
GSE16446
ID:
200016446
16.

Specific kinesin expression profiles associated with taxane resistance in breast cancer

(Submitter supplied) Purpose: Breast cancer is a genetically heterogenous disease with subtypes differing in prognosis and chemosensitivity. The basal-like breast cancer (BLBC) molecular subtype is associated with poorer outcomes, but is more responsive to taxane-based chemotherapy. We evaluated the role of kinesins, motor proteins interacting with microtubules, in influencing taxane resistance. Experimental Design: Kinesin (KIF) expression was studied in one local dataset comprising all taxane resistant breast cancers in relation to taxane resistance. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
24 Samples
Download data: TXT
Series
Accession:
GSE22796
ID:
200022796
17.

Modeling Luminal breast cancer heterogeneity: Combination therapy to suppress hormone receptor negative cells in Luminal disease

(Submitter supplied) Many Luminal breast cancers are heterogeneous, containing substantial numbers of estrogen (ER-) and progesterone (PR-) receptor-negative cells among the ER+PR+ ones. Currently, the Basal-like ER-PR- Luminobasal subpopulation in Luminal disease is not targeted for treatment. To address the relationships between ER+PR+ and ER-PR- cells in Luminal cancers and tightly control their ratios, we have generated isogenic pure Luminal (pLUM) and pure Luminobasal (pLB) cells from the same parental Luminal human breast cancer cell line. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13497
6 Samples
Download data: TXT, XLS
Series
Accession:
GSE55350
ID:
200055350
18.

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
19.

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
20.

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
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