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Links from GEO DataSets

Items: 17

1.

Gene expression profile of hedgehog-responsive stromal cells in mouse PB-MYC prostate tumor and normal prostate

(Submitter supplied) We report the application of RNA-sequencing for high-throughput profiling of gene expression in hedgehog-responsive stromal cells in normal mouse prostate and mouse prostate tumors. By using the Gli1-GFP knock-in reporter mouse line, we isolated the subset of mouse prostate stromal cells undergoing hedgehog signaling to compare the transcriptomes between PB-MYC prostate tumor and normal prostate in mice at the age of about 45 weeks.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: XLS
Series
Accession:
GSE92301
ID:
200092301
2.

Inflammation leads to loss of smooth muscle cells but fails to induce invasiveness in a prostate tumor model

(Submitter supplied) Inflammation has a causal role in many cancers. In prostate cancers, epidemiological data suggest a link between prostatitis and subsequent cancer development, but a proof for this concept in a tumor model has been lacking. A constitutively active version of the IkappaB kinase 2 (IKK2), the molecule activated by a plethora of inflammatory stimuli, was expressed specifically in the prostate epithelium. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4119
Platform:
GPL6246
6 Samples
Download data: CEL
Series
Accession:
GSE26410
ID:
200026410
3.
Full record GDS4119

Model for inflammatory signaling in prostate epithelium based on expression of a constitutively active version of IκB kinase 2 (IKK2ca)

Analysis of prostate epithelium (PE)-PTEN+/-IKK2ca/ca and PE-PTEN+/- lateral prostates. PE-PTEN+/-IKK2ca prostates exhibit loss of smooth muscle but fail to induce invasiveness. Results provide insight into the molecular mechanism of inflammation and tumor development in the transgenic prostates.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE26410
6 Samples
Download data: CEL
4.

TBX18 regulates the differentiation of periductal smooth muscle stroma and the maintenance of epithelial integrity in the prostate

(Submitter supplied) The T-box transcription factor TBX18 is essential to mesenchymal cell differentiation in several tissues and Tbx18 loss-of-function results in dramatic organ malformations and perinatal lethality. Here we demonstrate for the first time that Tbx18 is required for the normal development of periductal smooth muscle stromal cells in prostate, particularly in the anterior lobe, with a clear impact on prostate health in adult mice. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE80083
ID:
200080083
5.

Stromal androgen and hedgehog signaling regulates stem cell niches in pubertal prostate development

(Submitter supplied) Androgen-signaling is essential for prostate development. However, how androgen action facilitates prostatic stem/progenitor initiated pubertal prostatic growth remains unclear. Here, we demonstrate that androgens regulate Shh-signaling to control the cellular niche in prostatic epithelial development. Selective deletion of androgen receptor (AR) in stromal Shh-responsive cells significantly impedes pubertal prostatic epithelial morphogenesis and growth. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
2 Samples
Download data: TXT
Series
Accession:
GSE156168
ID:
200156168
6.

Gene expression in murine colon mucosa following activation of stromal Hedgehog signalling

(Submitter supplied) In the intestine, Hedgehog (Hh) signalling orchestrates epithelial homeostasis in a bidirectional loop. Differentiated enterocytes secrete the ligand leading to active downstream signaling exclusively in the stroma. In turn, Hh-driven stromal factors contribute to the control of intestinal stem cell numbers and induce epithelial differentiation. To investigate the consequences of stromal Hh activation on the gene expression level, we performed microarray analysis on full-thickness colonic tissue from Col1a2CreER;Ptch1fl/fl mice (C57BL/6 background). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
8 Samples
Download data: CEL
Series
Accession:
GSE67172
ID:
200067172
7.

Expression data from colon fibroblasts treated with Sonic hedgehog homolog (SHH)

(Submitter supplied) Canonical Hedgehog (Hh) signaling regulates the expression of genes that are critical to the patterning and development of a variety of organ systems. In adult, both ligand-dependent and ligand-independent Hh pathway activation are known to promote tumorigenesis. Recent studies have shown that in tumors promoted by Hh ligand, activation occurs within the stromal microenvironment (Yauch et al., 2009). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4512
Platform:
GPL570
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE29316
ID:
200029316
8.
Full record GDS4512

Sonic hedgehog homolog-stimulated fibroblasts

Analysis of CCD-18Co colon myofibroblasts stimulated with Sonic hedgehog homolog (SHH) for 72hr. Hedgehog (Hh)-driven, CCD-18Co proangiogenic signals drive tumor angiogenesis in vitro and in vivo. Results provide insight into the molecular mechanisms underlying Hh regulation of tumor angiogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent sets
Platform:
GPL570
Series:
GSE29316
6 Samples
Download data: CEL
9.

Epigenetic regulation of mammalian Hedgehog signaling to the stroma determines the molecular subtype of human bladder cancer

(Submitter supplied) In bladder, loss of mammalian Sonic Hedgehog (Shh) accompanies progression to invasive urothelial carcinoma, but the molecular mechanisms underlying this cancer-initiating event are poorly defined. Here, we show that loss of Shh results from hypermethylation of the CpG shore of the Shh gene, and that inhibition of DNA methylation increases Shh expression to halt the initiation of murine urothelial carcinoma at the early stage of progression. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
20 Samples
Download data: XLSX
Series
Accession:
GSE129441
ID:
200129441
10.

Gene expression profiling of laser capture microdissected prostate specimens

(Submitter supplied) We performed gene expression profiling of laser capture microdissected normal non-neoplastic prostate (cystoprostatectomies) epithelial tissue and compared it to non-transformed and neoplastic low and high grade prostate epithelial tissue from radical prostatectomies, each with its immediately surrounding stroma.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
188 Samples
Download data: CEL
Series
Accession:
GSE97284
ID:
200097284
11.

Non-Canonical Hedgehog Signaling Mediates Profibrotic Hematopoiesis-Stroma Crosstalk in Myeloproliferative Neoplasms

(Submitter supplied) We sorted lineage negative hematopoietic cells from mice previously transplanted with WT or Gli1 knockout bone marrow in both control and fibrosis settings. Cells were via magnetic depletion and facs sorting and performed scRNAseq on them. We identified 13 hematopoetic cells clusters across all lineages and one non-hematopoietic stromal cell cluster
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: MTX, TSV
Series
Accession:
GSE218616
ID:
200218616
12.

Distinct mesenchymal cell states mediate prostate cancer progression [Spatial Transcriptomics]

(Submitter supplied) We sought to determine whether molecular alterations in tumor stroma influence prostate cancer progression and metastatic potential. To accomplish this, we compared mesenchymal cells from four genetically engineered mouse models (GEMMs) of prostate cancer representing different stages of the disease to their wild-type (WT) counterparts by single-cell RNA sequencing (scRNA-seq) and, ultimately, to human tumors with comparable genotypes. more...
Organism:
Mus musculus
Type:
Other
Platform:
GPL24247
2 Samples
Download data: H5, TIFF
Series
Accession:
GSE248466
ID:
200248466
13.

Distinct mesenchymal cell states mediate prostate cancer progression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24676 GPL24247
48 Samples
Download data: H5, TIFF
Series
Accession:
GSE244270
ID:
200244270
14.

Distinct mesenchymal cell states mediate prostate cancer progression (mouse)

(Submitter supplied) We sought to determine whether molecular alterations in tumor stroma influence prostate cancer progression and metastatic potential. To accomplish this, we compared mesenchymal cells from four genetically engineered mouse models (GEMMs) of prostate cancer representing different stages of the disease to their wild-type (WT) counterparts by single-cell RNA sequencing (scRNA-seq) and, ultimately, to human tumors with comparable genotypes. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
17 Samples
Download data: H5AD
Series
Accession:
GSE244269
ID:
200244269
15.

Distinct mesenchymal cell states mediate prostate cancer progression (human)

(Submitter supplied) We sought to determine whether molecular alterations in tumor stroma influence prostate cancer progression and metastatic potential. To accomplish this, we compared mesenchymal cells from four genetically engineered mouse models (GEMMs) of prostate cancer representing different stages of the disease to their wild-type (WT) counterparts by single-cell RNA sequencing (scRNA-seq) and, ultimately, to human tumors with comparable genotypes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
29 Samples
Download data: H5AD
Series
Accession:
GSE244267
ID:
200244267
16.

Transcriptional analysis of the effect of monoamine oxidase B (MAOB) in human prostate stromal cells (PrSC)

(Submitter supplied) The overall goal of this study was to compare gene expression profiles in MOAB-overexpressing PrSC cells and control cells, also to compare gene expression profiles in MAOB-knockdown and control cells.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
5 Samples
Download data: TXT
17.

Transcription landscape of adipose tissue and tumor in response to adipose stromal cell depletion

(Submitter supplied) Mice grafted with Myc-Cap tumor were treated (3 weeks) with a pro-apoptotic peptide D-CAN targeting adipose stromal cells or PBS (control).
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21626
4 Samples
Download data: H5, MTX, TSV
Series
Accession:
GSE163701
ID:
200163701
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