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Links from GEO DataSets

Items: 20

1.

Expression of microRNAs and their gene targets are dysregulated in pre-invasive breast cancer (mRNA)

(Submitter supplied) Introduction: microRNAs (miRNAs) are short non-coding RNAs that negatively regulate gene expression and may play a causal role in invasive breast cancer. Since many genetic aberrations of invasive disease are detectable in earlier stages, we hypothesized that miRNA expression dysregulation and the predicted changes in gene expression would also be found in early breast neoplasias. Methods: Expression profiling of 365 miRNAs by RT-qPCR was combined with laser-capture microdissection to obtain an epithelial specific miRNA expression signature of normal breast epithelium (n=9) and of paired samples of histologically normal epithelium (HN) and ductal carcinoma in situ (DCIS) (n=16). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
2 Samples
Download data: CEL
Series
Accession:
GSE24506
ID:
200024506
2.

Expression of microRNAs and their gene targets are dysregulated in pre-invasive breast cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Other
Platforms:
GPL96 GPL10349
21 Samples
Download data: CEL, TXT
Series
Accession:
GSE24509
ID:
200024509
3.

Expression of microRNAs and their gene targets are dysregulated in pre-invasive breast cancer (microRNA)

(Submitter supplied) Introduction: microRNAs (miRNAs) are short non-coding RNAs that negatively regulate gene expression and may play a causal role in invasive breast cancer. Since many genetic aberrations of invasive disease are detectable in earlier stages, we hypothesized that miRNA expression dysregulation and the predicted changes in gene expression would also be found in early breast neoplasias. Methods: Expression profiling of 365 miRNAs by RT-qPCR was combined with laser-capture microdissection to obtain an epithelial specific miRNA expression signature of normal breast epithelium (n=9) and of paired samples of histologically normal epithelium (HN) and ductal carcinoma in situ (DCIS) (n=16). more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL10349
19 Samples
Download data: TXT
Series
Accession:
GSE24508
ID:
200024508
4.

Ductal Carcinoma Progression

(Submitter supplied) To obtain insight into the molecular basis of ductal carcinoma in situ (DCIS) and its progression by infiltrating surrounding tissue, we have performed cellular-based gene expression analysis of pure DCIS and DCIS with co-existing invasive ductal carcinoma (IDC) and compared the histological and molecular aspects between these morphologically identical lesions seeking to find key genes involved in DCIS progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1930
60 Samples
Download data
Series
Accession:
GSE11042
ID:
200011042
5.

Early Dysregulation of Cell Adhesion and Extracellular Matrix Pathways in Breast Cancer Progression

(Submitter supplied) Proliferative breast lesions, such as simple ductal hyperplasia (SH) and atypical ductal hyperplasia (ADH), are candidate precursors to ductal carcinoma in situ (DCIS) and invasive cancer. To better understand their relationship to more advanced disease, we used microdissection and DNA microarrays to profile the gene expression of patient-matched histologically normal (HN), ADH, and DCIS from 12 patients with ER+ sporadic breast cancer. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
40 Samples
Download data: CEL
Series
Accession:
GSE16873
ID:
200016873
6.

mRNA profiles in formalin-fixed and paraffin embedded (FFPE) breast cancer tissues

(Submitter supplied) we describe a mRNA profiling analysis of matched ductal carcinoma in situ and invasive duct carcinoma components of FFPE breast carcinomas with the purpose to identify potential prognostic markers
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8432
42 Samples
Download data: TXT
Series
Accession:
GSE72205
ID:
200072205
7.

Differentially expressed genes in human brest cancer specimens

(Submitter supplied) To identify differentially expressed genes in human brest cancer specimens were subjected to Agilent whole genome microarrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL20844
4 Samples
Download data: TXT
Series
Accession:
GSE118539
ID:
200118539
8.

Expression data from MCF-7 cells transfected with miR-26a and treated or not with estradiol

(Submitter supplied) Altered expression of microRNAs (miRNAs), an abundant class of small non-protein-coding RNAs that mostly function as negative regulators of protein-coding gene expression, is common in cancer. Here we analyze the regulation of miRNA expression in response to estrogen, a steroid hormone that is involved in the development and progression of breast carcinomas and that is acting via the estrogen receptors (ER) transcription factors. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
9 Samples
Download data: CEL
Series
Accession:
GSE17460
ID:
200017460
9.

Gene Expression Profiling of Tumor Microenvironment during Breast Cancer Progression

(Submitter supplied) To better understand the role of tumor microenvironment in breast cancer progression, we combined laser capture microdissection and microarray analysis to provide a comprehensive catalog of gene expression changes in both tumor and tumor-associated stroma. Keywords: cancer vs. normal
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1352
66 Samples
Download data: CEL
Series
Accession:
GSE14548
ID:
200014548
10.

Differentially Expressed Genes Regulating the Progression of Ductal Carcinoma In Situ to Invasive Breast Cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL1352 GPL8300
126 Samples
Download data: CEL
Series
Accession:
GSE41228
ID:
200041228
11.

Differentially Expressed Genes Regulating the Progression of Ductal Carcinoma In Situ to Invasive Breast Cancer (Group 4 Epithelial)

(Submitter supplied) We used gene expression profiling of human DCIS and IBC to discover uniquely expressed genes that may also regulate progression.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1352
22 Samples
Download data: CEL, TXT
Series
Accession:
GSE41227
ID:
200041227
12.

Differentially Expressed Genes Regulating the Progression of Ductal Carcinoma In Situ to Invasive Breast Cancer (Group 4 stroma)

(Submitter supplied) We used gene expression profiling of human DCIS and IBC to discover uniquely expressed genes that may also regulate progression.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1352
22 Samples
Download data: CEL, TXT
Series
Accession:
GSE41198
ID:
200041198
13.

Differentially Expressed Genes Regulating the Progression of Ductal Carcinoma In Situ to Invasive Breast Cancer (Group 3)

(Submitter supplied) We used gene expression profiling of human DCIS and IBC to discover uniquely expressed genes that may also regulate progression.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8300
18 Samples
Download data: CEL, TXT
Series
Accession:
GSE41197
ID:
200041197
14.

Differentially Expressed Genes Regulating the Progression of Ductal Carcinoma In Situ to Invasive Breast Cancer (Group 2)

(Submitter supplied) We used gene expression profiling of human DCIS and IBC to discover uniquely expressed genes that may also regulate progression.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8300
14 Samples
Download data: CEL, TXT
Series
Accession:
GSE41196
ID:
200041196
15.

Differentially Expressed Genes Regulating the Progression of Ductal Carcinoma In Situ to Invasive Breast Cancer (Group 1)

(Submitter supplied) We used gene expression profiling of human DCIS and IBC to discover uniquely expressed genes that may also regulate progression.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8300
50 Samples
Download data: CEL, TXT
Series
Accession:
GSE41194
ID:
200041194
16.

Whole genome DASL analysis of tumour epithelial and stromal compartments during breast cancer progression

(Submitter supplied) Analysis of gene expression changes in tumour epithelium (DCIS and invasive breast cancer) and stroma both immediately surrounding the lesions and more distantly.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
67 Samples
Download data: TXT
Series
Accession:
GSE35019
ID:
200035019
17.

H3K27ac ChIP-seq of MCF10A progression series

(Submitter supplied) This study takes an unbiased global analysis of super-enhancers that are acquired or lost in progression of breast cancer using the MCF10a progression series
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
16 Samples
Download data: BEDGRAPH
Series
Accession:
GSE181524
ID:
200181524
18.

Impact of BHLHE40-AS1 over expression in MCF10A cells

(Submitter supplied) BHLHE40-AS1 was cloned into pBABE-Puro. Empty vector and pBABE-BHLHE40-AS1 were used to generate retrovirus and infect MCF10A cells. Transduced cells were selected with 1ug/mL puromycin for 2 weeks.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL24539
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE136579
ID:
200136579
19.

Gene expression profiling of patient's DCIS-IDC tandem lesions by RNA sequencing analysis

(Submitter supplied) Tandem DCIS/IDC are defined as ductal carcicnoma in situ (DCIS) lesions that have concurrent invasive ductal carcinoma (IDC) within the same breast. These are identified radiologically by an area of clustered microcalcifications adjacent to (contiguous with) an invasive mass. Our radiologist (Dr. William P. Smith) has provided us with biopsy cores from each region. One core from each region (DCIS and IDC) has bas been collected and subjected to RNA sequencing for our studies to compare changes from DCIS to IDC in each individual patient.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: XLSX
20.

Restoring miR-200c to aggressive endometrial cancer cell line

(Submitter supplied) Using a mimic miR-200c was restored to an aggressive, Type 2 endometrial cancer cell line, Hec50
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
9 Samples
Download data: CEL
Series
Accession:
GSE25332
ID:
200025332
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