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Links from GEO DataSets

Items: 20

1.

SMARCA4/Brg1 Coordinates Genetic and Epigenetic Networks Underlying Shh-type Medulloblastoma Development [gene expression]

(Submitter supplied) Medulloblastoma could be classified into four subtypes: Wnt, Shh, Group 3, and Group 4. Subtypes of medulloblastoma have distinct epigenetic properties. We report that a chromatin regulator SMARCA4/Brg1 controls a transcriptional program that specifically required for Shh-type medulloblastoma identity and proliferation. We show that Brg1 deletion significantly inhibited tumor formation and progression in a mouse medulloblastoma model. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: TXT
Series
Accession:
GSE69672
ID:
200069672
2.

SMARCA4/Brg1 Coordinates Genetic and Epigenetic Networks Underlying Shh-type Medulloblastoma Development

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
4 Samples
Download data: BED, TXT
Series
Accession:
GSE69674
ID:
200069674
3.

SMARCA4/Brg1 Coordinates Genetic and Epigenetic Networks Underlying Shh-type Medulloblastoma Development [ChIP-Seq]

(Submitter supplied) Medulloblastoma could be classified into four subtypes: Wnt, Shh, Group 3, and Group 4. Subtypes of medulloblastoma have distinct epigenetic properties. We report that a chromatin regulator SMARCA4/Brg1 controls a transcriptional program that specifically required for Shh-type medulloblastoma identity and proliferation. We show that Brg1 deletion significantly inhibited tumor formation and progression in a mouse medulloblastoma model. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
2 Samples
Download data: BED
Series
Accession:
GSE69673
ID:
200069673
4.

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
5.

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
6.

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
7.

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
8.

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
9.

The lateral cerebellum is preferentially sensitive to high sonic hedgehog signaling and medulloblastoma formation

(Submitter supplied) The main cell of origin of the Sonic hedgehog (SHH) subgroup of medulloblastoma (MB) is granule cell precursors (GCPs), a SHH-dependent transient amplifying population in the developing cerebellum. SHH-MBs can be further subdivided based on molecular and clinical parameters, as well as location since SHH-MBs occur preferentially in the lateral cerebellum (hemispheres). Our analysis of adult patient data suggests that tumors with Smoothened (SMO) mutations form more specifically in the hemispheres than those with Patched 1 (PTCH1) mutations. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
12 Samples
Download data: CEL
Series
Accession:
GSE110932
ID:
200110932
10.

MYC overexpression and SMARCA4 loss cooperate to drive medulloblastoma formation in mice

(Submitter supplied) Group 3 medulloblastoma is one of the most aggressive types of childhood brain tumors. Roughly 30% of cases carry genetic alterations in MYC, SMARCA4, or both genes combined. While overexpression of MYC has previously been shown to drive medulloblastoma formation in mice, the functional significance of SMARCA4 mutations and their suitability as a therapeutic target remain largely unclear. To address this issue, we combined overexpression of MYC with a loss of SMARCA4 in granule cell precursors. more...
Organism:
Mus musculus
Type:
Methylation profiling by array
Platform:
GPL30650
3 Samples
Download data: IDAT, TXT
Series
Accession:
GSE235924
ID:
200235924
11.

MYC overexpression and SMARCA4 loss cooperate to drive medulloblastoma formation in mice

(Submitter supplied) Group 3 medulloblastoma is one of the most aggressive types of childhood brain tumors. Roughly 30% of cases carry genetic alterations in MYC, SMARCA4, or both genes combined. While overexpression of MYC has previously been shown to drive medulloblastoma formation in mice, the functional significance of SMARCA4 mutations and their suitability as a therapeutic target remain largely unclear. To address this issue, we combined overexpression of MYC with a loss of SMARCA4 in granule cell precursors. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
10 Samples
Download data: CSV, TXT
Series
Accession:
GSE235625
ID:
200235625
12.

The stem cell-associated transcription co-factor, ZNF521, interacts with GLI1 and GLI2 and enhances the activity of the Sonic hedgehog pathway

(Submitter supplied) ZNF521 is a transcription co-factor with recognized regulatory functions in haematopoietic, osteo-adipogenic and neural progenitor cells. Among its diverse activities, ZNF521 has been implicated in the regulation of medulloblastoma (MB) cells, where the Hedgehog (HH) pathway, has a key role in the development of normal cerebellum and of a substantial fraction of MBs. Here a functional cross-talk is shown for ZNF521 with the HH pathway, where it interacts with GLI1 and GLI2, the major HH transcriptional effectors and enhances the activity of HH signalling. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: TXT
13.

Atoh1 inhibits neuronal differentiation and collaborates with Gli1 to generate medulloblastoma-initiating cells

(Submitter supplied) The morphogen and mitogen, Sonic Hedgehog, activates a Gli1-dependent transcription program that drives proliferation of granule neuron progenitors (GNPs) within the external germinal layer of the postnatally developing cerebellum. Medulloblastomas with mutations activating the Sonic Hedgehog signaling pathway preferentially arise within the external germinal layer, and the tumor cells closely resemble GNPs. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
14 Samples
Download data: CEL
Series
Accession:
GSE19684
ID:
200019684
14.

A macrophage autonomous α4β1integrin-Syk-Rac2 signaling axis controls macrophage differentiation, tumor growth and metastasis

(Submitter supplied) Macrophages, play an essential role in promoting tumor growth by affecting angiogenesis, immune suppression, invasion and metastasis. The signal transduction events within macrophages which encode the complex cascade of events required for tumor growth and polarization of macrophages are poorly understood. We have discovered an ECM dependent signaling pathway in macrophages that regulates M2 macrophage differentiation, tumor growth, invasion and metastasis. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
12 Samples
Download data: CEL
Series
Accession:
GSE41717
ID:
200041717
15.

Novel mutations target distinct subgroups of medulloblastoma.

(Submitter supplied) Medulloblastoma is a malignant childhood brain tumour comprising four discrete subgroups. To identify mutations that drive medulloblastoma we sequenced the entire genomes of 37 tumours and matched normal blood. One hundred and thirty-six genes harbouring somatic mutations in this discovery set were sequenced in an additional 56 medulloblastomas. Recurrent mutations were detected in 41 genes not yet implicated in medulloblastoma: several target distinct components of the epigenetic machinery in different disease subgroups, e.g., regulators of H3K27 and H3K4 trimethylation in subgroup-3 and 4 (e.g., KDM6A and ZMYM3), and CTNNB1-associated chromatin remodellers in WNT-subgroup tumours (e.g., SMARCA4 and CREBBP). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4471
Platform:
GPL570
76 Samples
Download data: CEL
Series
Accession:
GSE37418
ID:
200037418
16.
Full record GDS4471

Medulloblastomas in children

Analysis of medulloblastomas from children ages 3 to 16 years. Medulloblastoma is a malignant childhood brain tumor comprising four discrete subgroups. Results provide insights into pathogenesis of medulloblastoma and highlight targets for therapeutic development.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 6 disease state, 2 gender, 4 other sets
Platform:
GPL570
Series:
GSE37418
76 Samples
Download data: CEL
17.

Expression data from GLI1-transformed RK3E cells

(Submitter supplied) SHH signaling pathway is activated in many type of cancers. However, the role of its activation in particular type of cancer was poorly understood. The GLI family transcription factor GLI1 is the effector of Shh pathway activation and functions as oncogene. Our goal of research is to identify the GLI1 targets in desmoplastic medulloblastomas. We used microarrays to obtain the global gene expression profiles in cells transformed by GLI1 and identified distinct classes of genes by comparing with those of desmoplastic medulloblastomas
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Dataset:
GDS3550
Platform:
GPL1355
6 Samples
Download data: CEL
Series
Accession:
GSE11987
ID:
200011987
18.
Full record GDS3550

GLI1 transformed kidney epithelial cell line

Analysis of kidney epithelial RK3E cells transformed by the oncogenic transcription factor GLI1. Results compared with the gene expression profile of a subgroup of medulloblastomas that shows constitutive activation of the Sonic hedgehog pathway with expression of GLI1.
Organism:
Rattus norvegicus
Type:
Expression profiling by array, count, 2 cell type, 3 other sets
Platform:
GPL1355
Series:
GSE11987
6 Samples
Download data: CEL
19.

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
20.

Transcriptomic changes induced by Gsk-3-deletion in cerebellar progenitors

(Submitter supplied) Cerebellar development requires regulated proliferation of cerebellar granule neuron progenitors (CGNPs). Inadequate CGNP proliferation causes cerebellar hypoplasia while excessive CGNP proliferation can cause medulloblastoma, the most common malignant pediatric brain tumor. Although Sonic Hedgehog (SHH) signaling is known to activate CGNP proliferation, the mechanisms down-regulating proliferation are less defined. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17400
15 Samples
Download data: CEL
Series
Accession:
GSE135463
ID:
200135463
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