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Links from GEO DataSets

Items: 20

1.

A mouse model of the most aggressive subgroup of human medulloblastoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL11180 GPL1261
79 Samples
Download data: CEL
Series
Accession:
GSE33201
ID:
200033201
2.

A mouse model of the most aggressive subgroup of human medulloblastoma [HT_MG-430_PM]

(Submitter supplied) A series of mouse models designed to mimic pediatric medulloblastoma types in humans were tested by microarray and compared to published human medulloblastoma data
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
15 Samples
Download data: CEL
Series
Accession:
GSE33200
ID:
200033200
3.

A mouse model of the most aggressive subgroup of human medulloblastoma [Mouse430_2]

(Submitter supplied) Mouse models of medulloblastoma are compared to human subgroups through microarray expression and other measures
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
64 Samples
Download data: CEL
Series
Accession:
GSE33199
ID:
200033199
4.

The miR-17/92 Polycistron Is Up-regulated in Sonic Hedgehog-Driven Medulloblastomas and Induced by N-myc in Sonic Hedgehog–Treated Cerebellar Neural Precursors

(Submitter supplied) Medulloblastoma is the most common malignant pediatric brain tumor, and mechanisms underlying its development are poorly understood. We identified recurrent amplification of the miR-17/92 polycistron proto-oncogene in 6% of pediatric medulloblastomas by high-resolution single-nucleotide polymorphism genotyping arrays and subsequent interphase fluorescence in situ hybridization on a human medulloblastoma tissue microarray. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
90 Samples
Download data: CEL
Series
Accession:
GSE21166
ID:
200021166
5.

Remodeling Group 3 medulloblastoma: MYC overexpression alone transforms progenitors of astrocytes and granule neurons in the postnatal cerebellum

(Submitter supplied) Group 3 medulloblastoma is often associated with MYC amplification or overexpression, while whether MYC overexpression alone is sufficient to induce tumorigenesis is unknown and the cell type(s) which can be transformed by MYC is unclear. Here, by generating a new mouse model, we demonstrated that overexpression of Myc alone is sufficient to transform astrocyte progenitors and granule neuron progenitors (GNP) in the early postnatal cerebellum following orthotopic transplantation. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21103
21 Samples
Download data: TXT
Series
Accession:
GSE114760
ID:
200114760
6.

Human neural stem cells transduced with oncogenic elements associated with aggressive medulloblastoma

(Submitter supplied) Human neural stem and progenitor cells transformed with c-MYC, dominant-negative p53, constitutively active AKT and hTERT formed tumors in mice that recapitulated Group 3 medulloblastoma in terms of pathology and expression profile
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
6 Samples
Download data: CEL
Series
Accession:
GSE77475
ID:
200077475
7.

An Animal Model of Myc-driven medulloblastoma

(Submitter supplied) Medulloblastoma (MB) is the most common malignant brain tumor in children. Patients whose tumors exhibit overexpression or amplification of the MYC oncogene (c-MYC) usually have an extremely poor prognosis, but there are no animal models of this subtype of the disease. Here we show that cerebellar stem cells expressing Myc and mutant Trp53 (p53) generate aggressive tumors following orthotopic transplantation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS4478
Platform:
GPL1261
19 Samples
Download data: CEL
Series
Accession:
GSE34126
ID:
200034126
8.
Full record GDS4478

MYC-driven medulloblastoma model

Analysis of Myc/DNp53-infected tumors derived from stem cells or progenitors, uninfected stem cells, and patched tumor cells. Cerebellar stem cells expressing Myc and mutant Trp53 generate tumors similar to MYC-driven medulloblastoma (MB). Results provide insight into transformation to MB tumor.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 4 cell type, 3 genotype/variation, 4 other sets
Platform:
GPL1261
Series:
GSE34126
19 Samples
Download data: CEL
9.

Myc and N-myc induce distinct medulloblastoma subgroups via Miz1

(Submitter supplied) Medulloblastomas (MBs) are cerebellar tumors that can be classified into molecularly distinct subgroups that differ in pathology and prognosis. The mechanisms that underlie subgroup specification are largely unknown. While human SHH MBs express MYCN, Group3 (G3) MBs are associated with c-MYC (MYC) overexpression and often show metastasis that confers a poor prognosis. Although MYC proteins are thought to be functionally exchangeable, ectopic expression of Myc or N-myc in Trp53-/-;Cdkn2c-/- cerebellar granule neuron progenitors (GNPs) induces G3 and SHH MBs, respectively, demonstrating that each Myc protein has distinct biological properties. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
24 Samples
Download data: CEL
Series
Accession:
GSE66093
ID:
200066093
10.

The MYC-MIZ1 interaction defines tumor identity

(Submitter supplied) Medulloblastoma (MB) is the most common malignant brain tumor. MB is a cerebellar tumor that occurs mostly in children between the ages of 3-7 years but also in adults. Human MBs are classified into four subgroups: Wingless (WNT), Sonic Hedgehog (SHH), Group 3 (G3) and G4, each of which with distinct molecular signatures. SHH MBs with MYCN amplification and TP53 mutations and G3 MBs characterized by C-MYC (MYC) overexpression in ~17% of cases from gene amplification with stem like properties, are the most aggressive and least curable with current therapeutic regimen. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL11002 GPL17021
23 Samples
Download data: BED, TXT, WIG
Series
Accession:
GSE64425
ID:
200064425
11.

Combined MYC and TP53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL6885 GPL13534
88 Samples
Download data: IDAT
Series
Accession:
GSE62626
ID:
200062626
12.

Combined MYC and TP53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease [gene expression]

(Submitter supplied) We undertook a comprehensive clinical and biological investigation of serial medulloblastoma biopsies obtained at diagnosis and relapse. Combined MYC gene family amplifications and P53 pathway defects commonly emerged at relapse, and all patients in this molecular group died of rapidly progressive disease post-relapse. To study this genetic interaction, we investigated a transgenic model of MYCN-driven medulloblastoma and found spontaneous development of Trp53 inactivating mutations. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6885
48 Samples
Download data: IDAT, TXT
Series
Accession:
GSE62625
ID:
200062625
13.

Methylation data from presentation and relapsed medulloblastoma tumour samples

(Submitter supplied) We undertook a comprehensive clinical and biological investigation of serial medulloblastoma biopsies obtained at diagnosis and relapse. Combined MYC gene family amplifications and P53 pathway defects commonly emerged at relapse, and all patients in this molecular group died of rapidly progressive disease post-relapse. To study this genetic interaction, we investigated a transgenic model of MYCN-driven medulloblastoma and found spontaneous development of Trp53 inactivating mutations. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
40 Samples
Download data: CSV
Series
Accession:
GSE62618
ID:
200062618
14.

Sonic Hedgehog subgroup medulloblastomas

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL9185 GPL6887
33 Samples
Download data: TXT
Series
Accession:
GSE98302
ID:
200098302
15.

Genome-wide transcriptional and epigenomic map of primary and metastatic Sonic Hedgehog subgroup medulloblastomas

(Submitter supplied) We report findings that illuminate a dynamic metastasis pathway in the common pediatric brain tumor medulloblastoma.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9185
12 Samples
Download data: BIGWIG
Series
Accession:
GSE98300
ID:
200098300
16.

Transcriptomic analysis of metastatic Sonic Hedgehog subgroup medulloblastomas

(Submitter supplied) We report findings that illuminate a dynamic metastasis pathway in the common pediatric brain tumor medulloblastoma.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9185
9 Samples
Download data: TXT
Series
Accession:
GSE98299
ID:
200098299
17.

Transcriptomic analysis of primary and metastatic Sonic Hedgehog subgroup medulloblastomas

(Submitter supplied) We report findings that illuminate a dynamic metastasis pathway in the common pediatric brain tumor medulloblastoma.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
12 Samples
Download data: TXT
Series
Accession:
GSE98298
ID:
200098298
18.

Pten deletion in neonatal brain induces an abnormal neural progenitor niche that can synergize with Trp53 loss to generate medulloblastoma

(Submitter supplied) To investigate Pten function in neonatal developing brain, we conditionally inactivated Pten in neural stem/progenitor cells at birth using a Nestin-CreER transgenic driver. Pten inactivation created a novel perivascular proliferative niche in the cerebellum that did not progress to malignancy during the lifespan of the mouse. Co-deletion of Pten and Trp53 synergized to cause fully penetrant medulloblastoma originating from a perivascular niche. more...
Organism:
Mus musculus
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL1261 GPL4714
33 Samples
Download data: CEL, GPR
Series
Accession:
GSE40106
ID:
200040106
19.

Genetic alterations in mouse medulloblastomas and generation of tumors from cerebellar grunule neuron precursors

(Submitter supplied) Mice lacking p53 and one or two alleles of the cyclin D-dependent kinase inhibitor p18Ink4c are prone to medulloblastoma development. The tumor frequency is increased by exposing postnatal animals to ionizing radiation at a time when their cerebella are developing. In irradiated mice engineered to express a floxed p53 allele and a Nestin-Cre transgene, tumor development can be restricted to the brain. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platforms:
GPL339 GPL340
10 Samples
Download data: CEL
Series
Accession:
GSE6463
ID:
200006463
20.

Microarray-based DNA methylation profiles of primary medulloblastomas

(Submitter supplied) Identification of novel molecular subgroups Background: International consensus recognises four medulloblastoma molecular subgroups - WNT, SHH, Group 3 and Group 4 - each defined by their characteristic genome-wide transcriptomic and DNA methylomic profiles. Subgroups harbor distinct clinico-pathological and molecular features, underpin current disease sub-classification and initial subgroup-directed therapies are underway in clinical trials (i.e. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
428 Samples
Download data: IDAT, TXT
Series
Accession:
GSE93646
ID:
200093646
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