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Items: 13

1.

Micro-scale genomic copy number aberrations as another means of mutagenesis in breast cancer

(Submitter supplied) Introduction: In breast cancers, the basal-like subtype has high levels of genomic instability relative to other breast cancer subtypes with many basal-like-specific regions of aberration. There is evidence that this genomic instability extends to smaller scale genomic aberrations as well, as shown by a previously described micro-event in the PTEN gene in the Basal-like SUM149 breast cancer cell line. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array; Genome variation profiling by genome tiling array
8 related Platforms
192 Samples
Download data
Series
Accession:
GSE36889
ID:
200036889
2.

MicroRNA-30c inhibits Human Breast Tumor Chemotherapy Resistance by regulating TWF1 and IL-11: Patient DataSet

(Submitter supplied) Chemotherapy resistance frequently drives tumor progression. However, the underlying molecular mechanisms are poorly characterized. Epithelial-to-mesenchymal transition (EMT) has been shown to correlate with therapy resistance, but the functional link and signaling pathways remain to be elucidated. We report here that miR-30c, a human breast tumor prognostic marker, plays a pivotal role in chemo-resistance by a direct targeting of the actin-transporter TWF1, which promotes EMT. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
6 related Platforms
60 Samples
Download data
Series
Accession:
GSE22049
ID:
200022049
3.

Basal-like Breast Cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival

(Submitter supplied) Breast cancer is a heterogeneous disease with known tumor subtypes. In order to gain insight into the underlying etiologies of these disease subtypes, we first classified tumors according to gene expression intrinsic subtype, and second, identified subtype associated tumor genomic DNA copy number alterations (CNA) using a novel method called SWITCHdna. Most tumor subtypes showed specific CNA with Basal-like breast cancers being the most distinct and associated with loss of RB1, BRCA1, 5q11-35, and showed the greatest overall genomic instability. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array; Genome variation profiling by SNP array
7 related Platforms
504 Samples
Download data
Series
Accession:
GSE10893
ID:
200010893
4.

Genomic analysis identifies unique signatures predictive of brain, lung, and liver relapse

(Submitter supplied) The ability to predict metastatic potential is of clinical and biological importance. Numerous metastasis/relapse predictors exist for breast cancer patients; however, what is less well established is whether predicting metastasis to specific organs sites is feasible. In this study we sought to determine: 1) the degree to which gene signatures vary across tumors and their metastases, 2) if genomic intrinsic subtypes associate with particular organs of relapse, and 3) if other genomic signatures can predict spread to specific organs. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
7 related Platforms
414 Samples
Download data
Series
Accession:
GSE26338
ID:
200026338
5.

Phenotypic and Molecular Characterization of the Claudin-low Intrinsic Subtype of Breast Cancer

(Submitter supplied) In breast cancer, gene expression analyses have defined five tumor subtypes, each of which has unique biologic and prognostic features. Here, we characterize the recently identified claudin-low tumor subtype as showing low to absent expression of luminal differentiation markers, high enrichment for epithelial-to-mesenchymal transition markers, immune response genes, and cancer stem cell–like features. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
7 related Platforms
372 Samples
Download data
Series
Accession:
GSE18229
ID:
200018229
6.

An integromic analysis reveals that metaplastic carcinomas are distinct from basal-like tumors.

(Submitter supplied) Metaplastic breast cancers (MBC) are aggressive, chemoresistant tumors characterized by lineage plasticity. To advance understanding of their pathogenesis and relatedness to other breast cancer subtypes, 28 MBCs were compared with common breast cancers using comparative genomic hybridization, transcriptional profiling, and reverse-phase protein arrays and by sequencing for common breast cancer mutations. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
4 related Platforms
244 Samples
Download data
Series
Accession:
GSE10885
ID:
200010885
7.

Identification of conserved gene expression features across human and murine mammary tumors

(Submitter supplied) Mice have been used as models for human breast cancers for many years, however, it is still unclear which murine models faithfully represent human tumor phenotypes. To address this question, we used DNA microarrays to characterize 10 different murine mammary models and compared these data to the expression patterns from primary human breast tumors. Hierarchical clustering analysis of the murine samples showed that the WAP-Myc, MMTV-Neu, MMTV-PyMT, WAP-Int3, and C3(1)-Tag tumors were highly correlated within each model. more...
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
4 related Platforms
354 Samples
Download data
Series
Accession:
GSE3165
ID:
200003165
8.

Biological Classification of Breast Cancer by Real-Time Quantitative RTPCR: Comparisons to Microarray and Histopathology

(Submitter supplied) Microarrays have shown that gene expression patterns can be used to molecularly classify breast cancers into distinct and clinically significant groups. In order to translate these profiles into routine diagnostics, we have recapitulated a microarray breast cancer classification using real-time quantitative (q)RT-PCR. We performed statistical analyses on multiple independent microarray datasets to select an “intrinsic” gene set that can classify breast tumors into four different subtypes designated as Luminal, Normal-like, HER2+/ER-, and Basal-like. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL885 GPL1390 GPL887
126 Samples
Download data
Series
Accession:
GSE2607
ID:
200002607
9.

A New Breast Tumor Intrinsic Gene List Identifies Novel Characteristics that are Conserved Across Microarray Platforms

(Submitter supplied) Breast cancer is a difficult disease to manage because it is comprised of a spectrum of tumor subtypes with different biological characteristics. Previous gene expression studies using breast tumor “intrinsic” gene lists identified five distinct subtypes of breast tumors: Luminal A, Luminal B, Normal Breast-like, HER2+/ER- and Basal-like. Using a training data set of 102 unique breast tumors, we derive a new “intrinsic” gene list based upon 26 paired samples. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL885 GPL1390 GPL887
170 Samples
Download data
Series
Accession:
GSE1992
ID:
200001992
10.

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
11.

Breast Tumor's study

(Submitter supplied) Microarray analysis has been shown to improve risk stratification of breast cancer. Breast tumors analyzed by hierarchical clustering of expression patterns of "intrinsic" genes have been reported to subdivide into at least four molecular subtypes that are associated with distinct patient outcomes. Using a supervised method, a 70-gene expression profile has been identified that predicts the later appearance or absence of clinical metastasis in young breast cancer patients. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL1390 GPL887 GPL885
169 Samples
Download data
Series
Accession:
GSE2741
ID:
200002741
12.

Agilent-011521 Human 1A Microarray G4110A (Feature Number version)

(Submitter supplied) Agilent's Human 1A Oligo Microarray (V2) includes over 17K 60-mer oligonucleotide probes, sourced from the Incyte Foundation Database and are designed to span conserved exons across the transcripts of the targeted full length genes. Coupled with Agilent's Arrays of this design have barcodes that begin with 16011521 or 2511521. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. more...
Organism:
Homo sapiens
35 Series
1 Related Platform
254 Samples
Download data: TXT
Platform
Accession:
GPL885
ID:
100000885
13.

BC00085

Organism:
Homo sapiens
Source name:
Stratagene Human Universal Reference that contained 1/10 added MCF7 and ME16C RNAs (channel 1) Breast Tumor (channel 2)
Platform:
GPL885
Series:
GSE1992 GSE2607 GSE2740 GSE2741 GSE3165 GSE10885 GSE10893 GSE18229 GSE22049 GSE26338 GSE36889
Download data
Sample
Accession:
GSM34509
ID:
300034509
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