U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 18

1.

DHT-dependent AR activity in LNCaP cells

(Submitter supplied) AR transcriptional activity is regulated by DHT
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
8 Samples
Download data: CEL
Series
Accession:
GSE60721
ID:
200060721
2.

Regulation of casodex-dependent AR activity by NCOR1

(Submitter supplied) Proliferation of prostate cancer cells, LNCaP, is suppressed by casodex. This suppression requires expression of AR coregulator, NCOR1.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE60722
ID:
200060722
3.

LNCaP cells: shRNA library with bicalutamide

(Submitter supplied) Short hairpin RNA library-based functional screening identified ribosomal protein L31 that modulates prostate cancer cell growth
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL14820
2 Samples
Download data: TXT
Series
Accession:
GSE60382
ID:
200060382
4.

Genome-wide impact of ART-27 loss on androgen-regulated transcription in prostate cancer cells

(Submitter supplied) The androgen receptor (AR) directs diverse biological processes through interaction with coregulators such as androgen receptor trapped clone-27 (ART-27). The impact of ART-27 on genome-wide transcription was examined. The studies indicate that loss of ART-27 enhances expression of many androgen-regulated genes, suggesting that ART-27 inhibits gene expression. Surprisingly, classes of genes that are upregulated upon ART-27 depletion include regulators of DNA damage checkpoint and cell cycle progression, suggesting that ART-27 functions to keep expression levels of these genes low. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
8 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE14043
ID:
200014043
5.

Modulators of Prostate Cancer Cell Proliferation and Viability Identified by Short-Hairpin RNA Library Screening

(Submitter supplied) Recovery of hairpins targeting a known prostate cancer pathway testing the utility of shRNA library screening in prostate cancer as a broad strategy to identify new candidate drug targets.
Organism:
Homo sapiens
Type:
Other
Platform:
GPL14596
56 Samples
Download data: TXT
Series
Accession:
GSE32261
ID:
200032261
6.

The E3 ubiquitin ligase Siah2 contributes to castration-resistant prostate cancer by regulation of androgen receptor transcriptional activity

(Submitter supplied) Analysis of gene expression altered upon knockdown of Siah2 in prosate cancer cells. The objective is to elucidate which signaling pathways or transcription factors are regulated by the E3 ubiquitin ligase Siah2 in human prostate cancer cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
4 Samples
Download data: TXT
Series
Accession:
GSE38851
ID:
200038851
7.

Single Cell mRNA Sequencing of Pca-associated CD14+CD11b+ macrophages

(Submitter supplied) Purpose: Androgen receptor (AR) is a crucial modulator of prostate cancer (PCa) cells behaviour, and AR expression has been found in several stromal cells, including macrophages, however its role in these cells in largely unknown. In this study, we described the molecular mechanims and the functional implications of AR activation and blockade in macrophages in relation to PCa progression. Results: Analysis showed the transcriptomic landscape of PCa-associated macrophages Conclusions: Our study represents the first detailed analysis of AR molecular function in Pca-associated macrophages
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
3 Samples
Download data: TSV
Series
Accession:
GSE133094
ID:
200133094
8.

Androgen Receptor Signalling in Macrophages Promotes TREM-1 mediated Cell Migration and Invasion pluripotent and lineage-committed cells.

(Submitter supplied) The Androgen Receptor (AR) is the master regulator of Prostate Cancer (PCa) development, and inhibition of AR signalling is the most effective PCa treatment. AR is expressed in PCa cells and also in the PCa-associated stroma, including infiltrating macrophages ). Macrophages play a decisive role in PCa initiation and progression, however, the role of AR in these cells remains largely unexplored. Here we show that AR signalling in macrophage-like THP-1 cell line supports PCa cell line migration and invasion in culture via increased Triggering REceptor of Macrophage-1 (TREM-1) signalling and expression of its downstream cytokines.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9052
8 Samples
Download data: TDF
Series
Accession:
GSE131381
ID:
200131381
9.

Nuclear Receptor Corepressor 1 (NCoR1) deletion changed the expression profile in cardiomyocytes

(Submitter supplied) NCoR1 played an important role in regulating the expression of many genes. We were wondering what kinds of genes the NCoR1 would regulate in cardiomyocytes. Therefore we generated the cardiomyocyte-specific NCoR1 knockout mice (CMNKO). Then we tried to analyze gene expression of left ventricular from littermate control (LC) and CMNKO mice with an unbiased way. Therefore the samples from left ventricular were subjected RNA-sequencing.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: XLS
Series
Accession:
GSE134923
ID:
200134923
10.

LNCaP Atlas: Gene expression associated with in vivo progression to castration-recurrent prostate cancer

(Submitter supplied) Background: There is no cure for castration-recurrent prostate cancer (CRPC) and the mechanisms underlying this stage of the disease are unknown. Methods: We analyzed the transcriptome of human LNCaP prostate cancer cells as they progress to CRPC in vivo using replicate LongSAGE libraries. We refer to these libraries as the LNCaP atlas and compared these gene expression profiles with current suggested models of CRPC. more...
Organism:
Homo sapiens
Type:
Expression profiling by SAGE
Platform:
GPL1485
9 Samples
Download data
Series
Accession:
GSE18402
ID:
200018402
11.

Single-cell RNA-seq reveals a subpopulation of prostate cancer cells with enhanced cell cycle-related transcription and attenuated androgen response

(Submitter supplied) Increasing evidence indicates that minor subpopulations intrinsic to androgen-independence are present in prostate cancer cells, poised to become clonal dominance under prolonged androgen-deprivation selection. To stratify different subpopulations, we conduct transcriptome profiling of 144 single LNCaP prostate cancer cells treated and untreated with androgen after cell cycle synchronization. At least eight subpopulations of LNCaP cells are identified, revealing a previously unappreciable level of cellular heterogeneity to androgen stimulation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
147 Samples
Download data: TXT
Series
Accession:
GSE99795
ID:
200099795
12.

NCOR1 sustains CRC growth and protects from cellular senescence

(Submitter supplied) The nuclear corepressor NCOR1 is a transcriptional repressor that regulates gene expression by associating with nuclear receptors or transcription factors such as AP-1 and NF-KB. The objective of this work was to determine how NCOR1 regulates proliferation and inflammatory response in human colorectal cancer cell lines. We observed that upon targeting NCOR1 expression from the use of shRNAs, Caco-2/15 and HT-29 colorectal cancer cells stopped proliferating with characteristics of being senescent. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: XLS
Series
Accession:
GSE174204
ID:
200174204
13.

The Fgf/Erf/NCoR1/2 repressive axis controls trophoblast cell fate

(Submitter supplied) Placental development relies on coordinated cell fate decisions governed by signalling inputs. However, little is known about how signalling cues are transformed into repressive lineage-specific transcriptional signatures. Here, we demonstrate that upon inhibition of the Fgf/Erk pathway in mouse trophoblast stem cells (TSCs), the Ets2 repressor factor (Erf) interacts with the Nuclear Receptor Corepressor Complex 1 and 2 (NCoR1/2) and recruits it to key trophoblast genes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24247 GPL17021
248 Samples
Download data: CSV, TXT
Series
Accession:
GSE199024
ID:
200199024
14.

Nuclear corepressors NCOR1/NCOR2 regulate B cell development, maintain genomic integrity, and prevent transformation

(Submitter supplied) The nuclear corepressors NCOR1 and NCOR2 interact with transcription factors involved in B cell development and potentially link these factors to alterations in chromatin structure and gene expression. Herein we demonstrate that NCOR1/2 deletion limits B cell differentiation via impaired recombination, attenuates pre-BCR-signaling, and enhances STAT5-dependent transcription. Furthermore, NCOR1/2-deficient B cells exhibited derepression of EZH2-repressed gene modules, including the p53 pathway. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
6 Samples
Download data: MTX, TXT
Series
Accession:
GSE208656
ID:
200208656
15.

Breast cancer plasticity is restrictedby a LATS1-NCOR1 repressive axis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL24247 GPL19057
16 Samples
Download data: BED
Series
Accession:
GSE195716
ID:
200195716
16.

Breast cancer plasticity is restrictedby a LATS1-NCOR1 repressive axis [MARS-seq]

(Submitter supplied) The tumor suppressor LATS1, whose expression is often downregulated in human breast cancer, helps maintain luminal breast cancer cell identity by keeping basal-specific genes in a closed chromatin state, preventing their spurious activation. This is achieved via interaction of LATS1 with the NCOR1 nuclear corepressor and recruitment of HDAC1,driving histone H3K27 deacetylation near NCOR1-repressed “basal” genes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
8 Samples
Download data: XLSX
Series
Accession:
GSE195715
ID:
200195715
17.

Breast cancer plasticity is restrictedby a LATS1-NCOR1 repressive axis [ATAC-seq]

(Submitter supplied) The tumor suppressor LATS1, whose expression is often downregulated in human breast cancer, helps maintain luminal breast cancer cell identity by keeping basal-specific genes in a closed chromatin state, preventing their spurious activation. This is achieved via interaction of LATS1 with the NCOR1 nuclear corepressor and recruitment of HDAC1,driving histone H3K27 deacetylation near NCOR1-repressed “basal” genes. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: BED
Series
Accession:
GSE195714
ID:
200195714
18.

A functional map of DNA-associated proteolysis

(Submitter supplied) We established an assay to localize DNA-associated proteins that are slated for degradation by the ubiquitin-proteasome system. The genome-wide map we describe here ties proteolysis to active enhancer elements and to transcription start sites of specific gene families.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: BIGWIG
Series
Accession:
GSE33821
ID:
200033821
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=3|blobid=MCID_66650e5ebb845b085be860c3|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center