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Links from GEO DataSets

Items: 20

1.

Expression data from murine brain tumors

(Submitter supplied) There is evidence that brain tumor cells may hijack self-renewal mechanism that regulate stem cell maintenance during normal development. Notch signaling is fundamental for maintaining normal neural stem cells in an undifferentiated state and has been implicated in in the maintenance of brain tumor stem cells as well. We used microarrays to detail the global gene expression program in murine brain tumors lacking RBPjk, an indispensable mediator of the Notch signaling pathway in the cell nucleus.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
16 Samples
Download data: CEL
Series
Accession:
GSE64230
ID:
200064230
2.

In vivo disruption of Rb-E2F-Ezh2 signaling loop causes bladder cancer development

(Submitter supplied) Bladder cancer (BC) is a highly prevalent human disease in which Rb pathway inactivation and epigenetic alterations are common events. However, the connection between these two processes is still poorly understood. Here we show that the in vivo inactivation of all Rb family genes in the mouse urothelium is sufficient to initiate BC development. The characterization of the mouse tumors revealed multiple molecular features of human BC, including the activation of E2F transcription factor and subsequent Ezh2 expression, and the activation of several signaling pathways previously identified as highly relevant in urothelial tumors. more...
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL6246 GPL6244
51 Samples
Download data: CEL
Series
Accession:
GSE38264
ID:
200038264
3.

Effect of tenascin C on brain tumor initiating cells

(Submitter supplied) We have determined that tenascin C (TNC) regulates the growth of human brain tumor initiating cells (BTICs). We have identified novel mechanisms by which TNC regulates BTIC growth. Analysis of the array data identified a number of genes that were altered with TNC treatment that could potentially regulate BTIC growth. The study provides the mechanistic basis for the regulation of BTIC growth with TNC.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE94640
ID:
200094640
4.

Surgical specimens of primary glioblastoma multiform: mRNA and miRNA profiling

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL8179 GPL6884
108 Samples
Download data
Series
Accession:
GSE25632
ID:
200025632
5.

Genome-wide analysis of microRNA expression in surgical specimens of primary glioblastoma multiform

(Submitter supplied) MicroRNA has a great potential in predicting survival of cancer patient. We used a genome-wide microRNA expression profiling to identify a miRNA signature for the prediction of clinical outcome of primary GBM patients.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8179
87 Samples
Download data: TXT
Series
Accession:
GSE25631
ID:
200025631
6.

Genome-wide analysis of gene expression in surgical specimens of primary glioblastoma multiform

(Submitter supplied) We used a genome-wide coding gene expression profiling to identify a gene signature for the molecular classification or prognostic prediction of primary GBMs.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6884
21 Samples
Download data: TXT
Series
Accession:
GSE25630
ID:
200025630
7.

Cooperative actions of p53 and Pten in normal and neoplastic progenitor cell renewal and differentiation

(Submitter supplied) Glioblastoma (GBM) is a highly lethal brain tumor presenting as one of two subtypes with distinct clinical histories and molecular profiles. The primary GBM subtype presents acutely as high-grade disease that typically harbors EGFR, PTEN and Ink4a/Arf mutations, and the secondary GBM subtype evolves from the slow progression of low-grade disease that classically possesses PDGF and p53 events1. Here, we show that concomitant CNS-specific deletion of p53 and Pten in the mouse CNS generates a penetrant acute-onset high-grade malignant glioma phenotype with striking clinical, pathological and molecular resemblance to primary GBM in humans. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
5 Samples
Download data: CEL
Series
Accession:
GSE12694
ID:
200012694
8.

Stem-like glioma-propagating cells contribute to molecular heterogeneity and survival outcome in oligodendroglial tumors

(Submitter supplied) Brain tumors are among the most malignant cancers and can arise from neural stem cells or oligodendrocyte progenitor cells (OPCs). Glioma-propagating cells (GPCs) that have stem-like properties have been derived from tumor variants such as glioblastoma multiforme (GBM) and oligodendroglial tumors, the latter being more chemosensitive with better prognosis. It has been suggested that such differences in chemosensitivity arise from the different profiles of OPCs versus neural stem cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4473
Platform:
GPL570
14 Samples
Download data: CEL
Series
Accession:
GSE31545
ID:
200031545
9.
Full record GDS4473

Glioblastoma multiforme and oligodendroglial glioma: neurospheres

Analysis of primary neurosphere cultures of glioblastoma (GBM) or oligodendroglial (ODG) tumors from 6 patients. Patient-derived glioma-propagating cells (GPC) contain karyotypic and gene expression profiles that are found in the primary tumor.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state, 6 individual, 2 other, 2 tissue sets
Platform:
GPL570
Series:
GSE31545
14 Samples
Download data: CEL
DataSet
Accession:
GDS4473
ID:
4473
10.

PDGF Engages an E2F-USP1 Signaling Pathway to Support ID2-mediated Survival of Proneural Glioma Cells.

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19441
12 Samples
Download data
Series
Accession:
GSE77424
ID:
200077424
11.

PDGF Engages an E2F-USP1 Signaling Pathway to Support ID2-mediated Survival of Proneural Glioma Cells.

(Submitter supplied) Identification of critical survival determinants of PDGF-driven proneural glioma. Results provided information about the genes and pathways that are regulated by PDGF signaling in PDGF-driven proneural glioma and led to the assessment of the importance of the USP1-ID2 axis in proneural glioma.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19441
6 Samples
Download data: TXT
Series
Accession:
GSE77423
ID:
200077423
12.

PDGF Engages an E2F-USP1 Signaling Pathway to Support ID2-mediated Survival of Proneural Glioma Cells.

(Submitter supplied) Identification of critical survival determinants of PDGF-driven proneural glioma. Results provided information about the genes and pathways that are regulated by PDGF signaling in PDGF-driven proneural glioma and led to the assessment of the importance of the USP1-ID2 axis in proneural glioma.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL19441
6 Samples
Download data: TXT
Series
Accession:
GSE77419
ID:
200077419
13.

RBPJ Maintains Brain Tumor Initiating Cells through CDK9-mediated Transcriptional Elongation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18573 GPL16791
18 Samples
Download data: BED
Series
Accession:
GSE79736
ID:
200079736
14.

RNA-seq Profiles in RBPJ Maintains Brain Tumor Initiating Cells through CDK9-mediated Transcriptional Elongation

(Submitter supplied) Glioblastomas coopt stem cell regulatory pathways to maintain brain tumor initiating cells (BTICs), also known as cancer stem cells. Notch signaling has been a molecular target in BTICs, but Notch antagonists have demonstrated limited efficacy in clinical trials. RBPJ is considered a central transcriptional mediator of Notch activity. Here, we report that pharmacologic Notch inhibitors were less effective than targeting RBPJ in suppressing tumor growth. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: TXT
15.

Epigenetic Profile in RBPJ Maintains Brain Tumor Initiating Cells through CDK9-mediated Transcriptional Elongation

(Submitter supplied) Glioblastomas display hierarchies with self-renewing cancer stem-like cells (CSCs). RNA sequencing and enhancer mapping revealed regulatory programs unique to CSCs causing upregulation of the iron transporter transferrin, the top differentially expressed gene compared to tissue-specific progenitors. Direct interrogation of iron uptake demonstrated CSCs potently extract iron from the microenvironment more effectively than other tumor cells. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: BED
Series
Accession:
GSE79734
ID:
200079734
16.

Transcriptome analysis of medulloblastoma tumors in mice

(Submitter supplied) The proto-oncogene MYCN is mis-expressed in various types of human brain tumors. To clarify how developmental and regional differences influence transformation, we transduced wild-type or mutationally-stabilized murine N-mycT58A into neural stem cells (NSCs) from perinatal murine cerebellum, brain stem and forebrain. Transplantation of Nmyc WT NSCs was insufficient for tumor formation. N-mycT58A cerebellar and brain stem NSCs generated medulloblastoma/primitive neuroectodermal tumors, whereas forebrain NSCs developed diffuse glioma. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6096
56 Samples
Download data: CEL
Series
Accession:
GSE36594
ID:
200036594
17.

QKI deficiency maintains stemness of glioma stem cells in suboptimal environment by downregulating endolysosomal degradation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
34 Samples
Download data: TXT
Series
Accession:
GSE84134
ID:
200084134
18.

Sequencing data of Photoactivatable Ribonucleoside-Enhanced Crosslinking and Immunoprecipitation (PAR-CLIP) of QKI-5 and QKI-6

(Submitter supplied) This study was designed to look for the RNAs that directly bind with QKI
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
2 Samples
Download data: TXT
Series
Accession:
GSE84132
ID:
200084132
19.

QKI's function in neural stem cells (NSCs) and pre-malignant NSCs (PM-NSCs) and transcriptome of Nestin-CreERT2 PtenLoxP/LoxP p53LoxP/LoxP QKILoxP/LoxP (QPP) mouse glioblastoma

(Submitter supplied) This study is to determine the impact of QKI deletion on transcriptomes of mouse NSC and PM-NSC and to analyze the transcriptomic profiles of Nestin-CreERT2 PtenLoxP/LoxP p53LoxP/LoxP QKILoxP/LoxP (QPP) mouse glioblastoma and to determine which subtypes these tumors belong to
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
32 Samples
Download data: TXT
Series
Accession:
GSE79889
ID:
200079889
20.

NOTCH/HES5 signaling exhibits distinct roles in MYC- and AKT-driven liver carcinogenesis

(Submitter supplied) Notch signaling plays a pivotal role in liver development and aberrant Notch signaling may lead to hepatocellular (HCC) or cholangiocellular carcinoma (CCA) development. Using whole exome sequencing of 54 human HCC samples, we discovered 19 somatic missense mutations in 15 different Notch pathway genes affecting 24.6% (14 of 57) of patients. Prediction of functional impact of these Notch pathway mutations revealed HES5-R31G to have high relevance.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL25683
24 Samples
Download data: CEL
Series
Accession:
GSE121362
ID:
200121362
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