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Links from GEO DataSets

Items: 20

1.
Full record GDS1390

Prostate cancer progression after androgen ablation

Analysis of prostate cancer progression following androgen ablation treatment. 10 treated androgen-independent primary prostate tumors compared to 10 untreated androgen-dependent primary prostate tumors. Results provide insight into progression of prostate cancer to aggressive androgen-independent
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL96
Series:
GSE2443
20 Samples
Download data: CEL, EXP
2.

Prostate cancer - comparison of androgen-dependent and -independent microdissected primary tumor

(Submitter supplied) Affymetrix U133A comparison of two groups (10 samples each): untreated (androgen-dependent) primary prostate cancer (Gleasons 5-9) and androgen-independent primary prostate cancer. All samples were microdissected for tumor cells only. Keywords = advanced prostate cancer Keywords = androgen-independence Keywords = laser capture microdissection Keywords = RNA amplification Keywords: other
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS1390
Platform:
GPL96
20 Samples
Download data: CEL, EXP
Series
Accession:
GSE2443
ID:
200002443
3.

Molecular Features of Hormone-Refractory Prostate Cancer Cells by Genome-wide Gene-expression Profiles

(Submitter supplied) To characterize the molecular features of clinical (Hormone-Refractory Prostate Cancers) HRPCs, we generated the precise gene-expression profiles of 25 clinical HRPCs and 10 hormone-sensitive prostate cancers (HSPCs) by genome-wide cDNA microarrays combining with laser microbeam microdisection. Keywords: disease status analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4747
35 Samples
Download data: TXT
Series
Accession:
GSE6811
ID:
200006811
4.

Longitudinal Analysis of Progression to Androgen Independence

(Submitter supplied) Following androgen ablation therapy (AAT), the vast majority of prostate cancer patients develop treatment resistance with a median time of 18-24 months to disease progression. To identify molecular targets that aid in prostate cancer cell survival and contribute to the androgen independent phenotype, we evaluated changes in LNCaP cell gene expression during 12 months of androgen deprivation. At time points reflecting critical growth and phenotypic changes, we performed Affymetrix expression array analysis to examine the effects of androgen deprivation during the acute response, during the period of apparent quiescence, and during the emergence of highly proliferative, androgen-independent prostate cancer cells (LNCaP-AI). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3358
Platform:
GPL570
16 Samples
Download data: CEL
Series
Accession:
GSE8702
ID:
200008702
5.
Full record GDS3358

Androgen deprivation effect on LNCaP prostate cancer cells: time course

Analysis of cultured LNCaP prostate cancer cells during 12 months of androgen deprivation. Following androgen ablation therapy, most prostate cancer patients develop treatment resistance. Results provide insight into prostate cancer cell survival and androgen-independence.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 growth protocol, 6 time sets
Platform:
GPL570
Series:
GSE8702
15 Samples
Download data: CEL
DataSet
Accession:
GDS3358
ID:
3358
6.

Intraprostatic Androgens and Androgen-Regulated Gene Expression Persist Following Testosterone Suppression

(Submitter supplied) Introduction: Androgen deprivation therapy (ADT) remains the primary treatment for advanced prostate cancer (PCa). The efficacy of ADT has not been rigorously evaluated by demonstrating suppression of prostatic androgen activity at the target tissue and molecular level. We determined the efficacy and consistency of medical castration in suppressing prostatic androgen levels and androgen-regulated gene-expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4766
12 Samples
Download data: GPR
Series
Accession:
GSE8466
ID:
200008466
7.

Human prostate cancer xenografts on intact mice or after castration.

(Submitter supplied) cDNA expression arrays on a panel of human prostate cancer xenografts. The xenografts can divided into three groups: 1) androgen-dependent, 2) androgen-independent with functional expression of the androgen receptor, 3) androgen-independent lacking functional expression of the androgen receptor. Four microarrays were performed per xenograft using tissue samples collected in separate experiments. Two samples were taken from intact male mice, whereas the other two samples were taken 1 to 2 weeks after castration. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2384
Platform:
GPL3349
52 Samples
Download data
Series
Accession:
GSE4084
ID:
200004084
8.

Prostate cancer cell line LNCaP treated for 2, 4, 6, 8 h with the synthetic androgen R1881 (1nM)

(Submitter supplied) Time series of the prostate cancer cell line LNCaP, treated for 2, 4, 6 and 8 hours with the synthetic androgen R1881. As control, the cells were cultured for 2, 4, 6 and 8 hours in the presence of the same concentration of solvent (ethanol). With this short treatment time, we aimed to identify mainly direct targets of the androgen receptor. LNCaP has a very low growth rate in steroid stripped medium and resumes growth on addition of androgens. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2034
Platform:
GPL3349
8 Samples
Download data
Series
Accession:
GSE4027
ID:
200004027
9.
Full record GDS2384

Xenograft model of prostate carcinoma progression

Analysis of prostate cancer (PC) xenografts collected from male mice up to 14 days after castration. The androgen receptor (AR) plays a pivotal role in the growth and survival of prostate carcinoma. Results provide insight into the role of selective adaptations of the AR pathway in PC progression.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array, log2 ratio, 4 disease state, 3 other, 10 protocol, 14 specimen sets
Platform:
GPL3349
Series:
GSE4084
52 Samples
Download data
DataSet
Accession:
GDS2384
ID:
2384
10.
Full record GDS2034

Prostate cancer cell line LNCaP response to synthetic androgen R1881: time course

Expression profiling of prostate cancer cell line LNCaP treated for up to 8 hours with the synthetic androgen R1881. LNCaP cells grow slowly in medium devoid of steroids but resume growth upon the addition of androgens. The study aims to identify direct targets of the androgen receptor.
Organism:
Homo sapiens
Type:
Expression profiling by array, log2 ratio, 4 time sets
Platform:
GPL3349
Series:
GSE4027
8 Samples
Download data
DataSet
Accession:
GDS2034
ID:
2034
11.

Hypoxia-independent downregulation of hypoxia inducible factor 1 targets by androgen deprivation therapy in prostate cancer.

(Submitter supplied) Hypoxia inducible factor 1 (HIF1) has been shown to cooperate with the androgen receptor (AR) in activation of oncogenic pathways in prostate cancer (PCa). Here we hypothesized that HIF1 also plays a role in PCa response to androgen deprivation therapy (ADT). Comparison of gene expression profiles of androgen exposed (AE) and androgen deprived (AD) CWR22 PCa xenografts identified 596 upregulated and 748 downregulated genes after ADT. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
6 Samples
Download data: TXT
Series
Accession:
GSE42868
ID:
200042868
12.

caArray_green-00001: Alterations in Gene Expression Profiles during Prostate Cancer Progression

(Submitter supplied) To identify molecular changes that occur during prostate tumor progression, we have characterized a series of prostate cancer cell lines isolated at different stages of tumorigenesis from C3(1)/Tag transgenic mice.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL20562
19 Samples
Download data: GPR
Series
Accession:
GSE69892
ID:
200069892
13.

Prostate Cancer Gene Expression Changes after Treatment with Neoadjuvant Dutasteride

(Submitter supplied) To identify molecular changes underlying the chemopreventive or tumor promoting effects of SRD5A inhibition, we profiled gene expression changes in benign prostate epithelium from patients with PCa treated with dutasteride, a dual SRD5A inhibitor. Subjects were aged 45-80 years with clinically localized PCa (T1C to T2b), Gleason score <7, and serum PSA 2.5-10 ng/dL. 81 men were randomized to immediate RP (n=25) or to dutasterdie at 0.5 mg (n=26) or 3.5 mg (n=24) orally per day for four months prior to RP. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4768
40 Samples
Download data: GPR
Series
Accession:
GSE9972
ID:
200009972
14.

Gene expression profiling of hormone resistant prostate cancer

(Submitter supplied) In this study we performed transcriptional profiling of transurethral resections of hormone resistant prostate cancer and compared it with benign prostatic hyperplasia (BPH), untreated localized prostate cancer and hormone sensitive prostate cancer. Keywords: time course; disease state analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL201
20 Samples
Download data
Series
Accession:
GSE5377
ID:
200005377
15.

Expression profiling of the mouse prostate after castration and hormone replacement

(Submitter supplied) In this study, we used microarray analysis to determine gene expression profile changes in the mouse prostate following castration and hormone replacement. We first identified genes with significant expression changes in each of these two processes and then generated a list of androgen responsive genes and a list of genes whose expression were inversely correlated with the presence of androgen. The analysis of this data set is described in Wang et al., Differentiation, 2006 Keywords: Time course
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2562
Platform:
GPL81
20 Samples
Download data: CEL
Series
Accession:
GSE5901
ID:
200005901
16.
Full record GDS2562

Prostate response to castration and subsequent hormone replacement

Analysis of prostate of animals following castration and subsequent hormone replacement with testosterone. Castration induces prostate involution, while hormone replacement induces regeneration. Results provide insight into the molecular mechanisms regulating prostatic involution and regeneration.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 4 protocol sets
Platform:
GPL81
Series:
GSE5901
20 Samples
Download data: CEL
DataSet
Accession:
GDS2562
ID:
2562
17.

Prostate Cancer–Associated Gene Expression Alterations Determined from Needle Biopsies

(Submitter supplied) To accurately identify gene expression alterations that differentiate neoplastic from normal prostate epithelium using an approach that avoids contamination by unwanted cellular components and is not compromised by acute gene expression changes associated with tumor devascularization and resulting ischemia.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL4767 GPL4764
31 Samples
Download data: GPR
Series
Accession:
GSE40373
ID:
200040373
18.

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
19.

Genomic alterations indicate tumor origin and varied metastatic potential of disseminated cells from prostate cancer

(Submitter supplied) Disseminated epithelial cells can be isolated from the bone marrow of a far greater frac-tion of prostate-cancer patients than the fraction of patients who progress to metastatic disease. To provide a better understanding of these cells, we have characterized their genomic altera-tions. We first present an array comparative genomic hybridization method capable of detecting genomic changes in the small number of disseminated cells (10-20) that can typically be ob-tained from bone-marrow aspirates of prostate-cancer patients. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL6737
89 Samples
Download data: GPR
Series
Accession:
GSE11155
ID:
200011155
20.

Androgen regulated gene expression in human prostate

(Submitter supplied) Androgens are a prequisite for the development of human prostate and prostate cancer. Androgen action is mediated via androgen receptor. Androgen ablation therapy is used for the treatment of metastasized prostate cancer. The aim of the study was to identify genes differentially expressed in benign human prostate, prostate cancer and in prostate tissue three days after castration. These genes are potential diagnostic and therapeutic targets for prostate cancer and benign prostatic hyperplasia. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
9 Samples
Download data: CEL
Series
Accession:
GSE32982
ID:
200032982
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