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Links from GEO DataSets

Items: 20

1.

Expression data from conditional Klf5 knockout Pten-null mouse prostates

(Submitter supplied) KLF5 is a basic transcription factor that regulates multiple biological processes, but its function in tumorigenesis appears contradictory in the current literature, with some studies showing tumor suppressor activity and others showing tumor promoting activity. In this study, we examined the function of Klf5 in prostatic tumorigenesis using mice with prostate specific deletion of Klf5 and Pten, both of which are frequently deleted in human prostate cancer. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
8 Samples
Download data: CEL
Series
Accession:
GSE58719
ID:
200058719
2.

Interuption of Klf5 acetylaiton at K358 affects tumor microenvironment in Pten deficient mouse prostates

(Submitter supplied) PTEN deficiency induces KLF5 acetylation; and the interruption of KLF5 acetylation orchestrates intricate interactions between cancer cells and CAFs that enhance FGFR1 signaling and promote tumor growth. Deacetylated KLF5 promotes tumor cells to secrete TNF, which stimulates inflammatory CAFs to release FGF9. Single-cell transcriptomic analysis reveals an enhanced FGF signaling from fibroblasts to cancer cells after the interruption of Klf5 acetylation.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
4 Samples
Download data: MTX, TSV
Series
Accession:
GSE262893
ID:
200262893
3.

Interuption of Klf5 acetylaiton at K358 affects gene expression profiles in Pten deficient mouse prostates

(Submitter supplied) Cancer associated fibroblasts (CAFs) play a pivotal role in tumor progression, but it remains elusive whether and how PTEN-deficient prostate cancers reprogram CAFs to overcome the barriers for tumor progression. Herein, we report that PTEN deficiency induces KLF5 acetylation; and interruption of KLF5 acetylation orchestrates intricate interactions between cancer cells and CAFs that enhance FGFR1 signaling and promote tumor growth. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
20 Samples
Download data: TXT
Series
Accession:
GSE253523
ID:
200253523
4.

Virtual Karyotyping of Androgen Insensitive Prostate Cancer

(Submitter supplied) We investigated chromosomal imbalances in samples from patients with androgen insensitive prostate cancer.
Organism:
Homo sapiens
Type:
SNP genotyping by SNP array; Genome variation profiling by SNP array
Platform:
GPL3718
4 Samples
Download data: CEL, CHP
Series
Accession:
GSE13439
ID:
200013439
5.

Transcriptional profiling of mouse prostate tumors with conditional mutations in the Pten, Apc, or Tgfbr2 genes

(Submitter supplied) We report the changes in gene expression in mouse prostate comparing normal wild type prostate to tumors generated by Cre mediated deletion of Pten or Apc, either with or without deletion of Tgfbr2. Pten single mutant tumors were isolated at either 8 weeks or 22 weeks of age, with high grade prostate intraepithelial neoplasia (HGPIN) as the main phenotype. Pten;Tgfbr2 double mutants were isolated at 8 weeks (primarily HGPIN), or at 11-14 weeks with extensive locally invasive cancer. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
25 Samples
Download data: CSV
Series
Accession:
GSE108017
ID:
200108017
6.

A constitutively activated form of the p110 beta isoform of PI3-kinase induces prostatic intraepithelial neoplasia in mice

(Submitter supplied) The global gene expression profiles of ventral prostates of wild type mice and p110 beta transgenic mice.
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4108
Platform:
GPL8321
8 Samples
Download data: CEL
Series
Accession:
GSE21543
ID:
200021543
7.
Full record GDS4108

Prostate response to activated form of p110β isoform of PI3-kinase

Analysis of ventral prostate from transgenics expressing a constitutively activated p110β allele in prostate. Activation of the p110β isoform causes mouse prostatic intraepithelial neoplasia (mPIN). Results provide insight into ability of an activated allele of p110β to induce prostatic tumor.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 disease state sets
Platform:
GPL8321
Series:
GSE21543
8 Samples
Download data: CEL
8.

Targeted Pten deletion plus p53-R270H mutation in mouse mammary epithelium induces aggressive claudin-low and basal-like breast cancer

(Submitter supplied) WAP-Cre:Ptenf/f:p53lox.stop.lox_R270H composite mice were generated by genetic crossing. In these mice, Pten is deleted and a R270H p53 mutation in the DNA binding domain is induced upon expression of Cre recombinase in pregnancy-identified alveolar progenitors. Tumors were characterized by histology, marker analysis, various bioinformatics methods, high-throughput (HTP) FDA-drug screen as well as orthotopic injection to quantify tumor initiating cells (TICs) and tail-vein injection to identify lung-metastasis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
31 Samples
Download data: CEL
Series
Accession:
GSE75989
ID:
200075989
9.

Next-generation sequencing facilitates quantitative analysis of AcKLF5 and unAcKLF5 transcriptomes in xenografts of DU-145 cell line

(Submitter supplied) KLF5 possesses both tumor-suppressing and tumor-promoting activities, though the mechanism controlling these opposing functions is unknown. In cultured non-cancerous epithelial cells, KLF5 converts from pro-proliferative to anti-proliferative activity upon TGFβ-induced acetylation, which sequentially alters the KLF5 transcriptional complex and the expression of genes such as p15 and MYC. In nude mice, KLF5 also suppressed tumor growth in an acetylation-dependent manner. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
3 Samples
Download data: TXT
10.

Gene expression profiling of prostate tissues and seminal vesicles from PB-Pten-NICD mice

(Submitter supplied) To investigate the identity of the tissue origin for metastases, we compared gene expression profiles of the prostate tissues and seminal vesicles from PB-Pten-NICD mice and those of 7 lung metastases from different mice. Three respective cell lines established from primary seminal vesicle tumors, primary prostate tumors, and lung metastases in PB-Pten-NICD mice were also included in the microarray analysis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL13912
24 Samples
Download data: TXT
Series
Accession:
GSE72549
ID:
200072549
11.

A basal specific microRNA promotes tumorigenesis in both basal and luminal cells of murine prostate gland

(Submitter supplied) Recent studies demonstrate both basal and luminal cells of the prostate gland can initiate tumorigenesis upon oncogenic transformation. However, it remains unclear how molecular mechanisms operating within each cell lineage contribute to the initiation and progression of the prostate cancer. Here we investigate functions of individual miRNAs using genetically engineered mouse models. By both quantitative miR-Seq and in situ hybridization, we identify microRNA-205 (miR-205) as the most highly expressed miRNA and specific to the basal cells in the prostate. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: XLSX
Series
Accession:
GSE75321
ID:
200075321
12.

Development of gene sets after deleting Rb or Rb and Pten in p53 null background primary prostate cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL11202 GPL10787
14 Samples
Download data: TXT
Series
Accession:
GSE68905
ID:
200068905
13.

Development of gene sets after deleting Rb and Pten in p53 null background primary prostate cells [Rb and Pten]

(Submitter supplied) Our findings suggested that cytokines were upregulated in p53 null primary prostate cells after deleting Rb and/or Pten. Rb and Pten deletion are important for prostate cancer progression.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
8 Samples
Download data: TXT
Series
Accession:
GSE68904
ID:
200068904
14.

Development of gene sets after deleting Rb in p53 null background primary prostate cells [Rb only]

(Submitter supplied) Our findings suggested that cytokines were upregulated in p53 null primary prostate cells after deleting Rb. Rb deletion is important for prostate cancer progression.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11202
6 Samples
Download data: TXT
Series
Accession:
GSE68903
ID:
200068903
15.

Over-expression and knockdown of KLF5

(Submitter supplied) Activation of the Ras/Erk pathway upregulates expression of the Kruppel-like Factor 5 (KLF5) transcription factor, and KLF5 is a downstream mediator of Ras oncogenic signaling. Specifically, in bladder and colon cancer cell lines KLF5 upregulates the Ras-pathway target gene cyclin D1, and facilitates entry into the S phase of the cell cycle. Ras mutations are common in lung cancer, but a role for KLF5 in lung tumorigenesis has not been defined. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
9 Samples
Download data: CEL
Series
Accession:
GSE16555
ID:
200016555
16.

Pten signaling in fibroblasts effects gene expression in endothelial and epithelial cells

(Submitter supplied) These experiments aim determine the effects of Pten signaling in fibroblasts on gene expression in other cell compartments in the mammary gland.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6096
12 Samples
Download data: CEL
Series
Accession:
GSE24501
ID:
200024501
17.

Identification of novel transcription factors that regulate prostate cancer cell metabolism

(Submitter supplied) To understand of the impact of KLF5 and NFYA on metabolism in prostate cancer cells
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
18 Samples
Download data: CSV
Series
Accession:
GSE151290
ID:
200151290
18.

TIP5 primes prostate luminal cells for the oncogenic transformation mediated by PTEN-loss

(Submitter supplied) Prostate cancer (PCa) is the second leading cause of cancer death in men. Its clinical and molecular heterogeneity and the lack of in vitro models outline the complexity of PCa in the clinical and research settings. We established an in vitro mouse PCa model based on organoid technology that takes into account the cell of origin and the order of events. Primary PCa with deletion of the tumor suppressor gene PTEN (PTEN-del) can be modeled through Pten-downregulation in mouse organoids. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
24 Samples
Download data: BIGWIG, BW, CSV
Series
Accession:
GSE131845
ID:
200131845
19.

Gene expression changes resulting from attenuation of Dicer activity

(Submitter supplied) Despite smaller primary tumor burdens, Pten-/-Dicer-/+ mice develop seminal vesicle obstruction at high penetrance by 32 weeks, which is in sharp contrast to that observed in Pten-/- mice. This phenomenon implies that tumors in Pten-/-Dicer-/+ mice are more locally invasive. To corroborate this invasive phenotype, we examined global changes in gene expression using Agilent 44k whole genome expression microarrays. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
12 Samples
Download data: TXT
Series
Accession:
GSE42820
ID:
200042820
20.

Expression data from control and COUP-TFII siRNA treated PC3 cells

(Submitter supplied) COUP-TFII, a member of the nuclear receptor superfamily plays a critical role in angiogenesis and organogenesis during embryonic development. Our results indicate that COUP-TFII expression is profoundly upregulated in prostate cancer patients and might serves as biomarker for recurrence prediction. Thus we conduct transcriptome comparison of control and COUP-TFII depleted PC3 cells to gain genomic insights on the biological processes that COUP-TFII is involved in prostate cancer cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE33182
ID:
200033182
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