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Links from GEO DataSets

Items: 20

1.

Zebrafish Samples for Loss of ATRX cooperates with p53-Deficiency to promote the Development of Sarcomas and other Malignancies

(Submitter supplied) The SWI/SNF-family chromatin remodeling protein ATRX is a tumor suppressor in sarcomas, gliomas and other malignancies. Its loss of function facilitates the alternative lengthening of telomeres (ALT) pathway in tumor cells, while it also affects Polycomb repressive complex 2 (PRC2) silencing of its target genes. To further define the role of inactivating ATRX mutations in carcinogenesis, we knocked out atrx in our previously published p53/nf1-deficient zebrafish line that develops malignant peripheral nerve sheath tumors and gliomas. more...
Organism:
Danio rerio
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20828
10 Samples
Download data: FPKM_TRACKING, TXT
Series
Accession:
GSE125040
ID:
200125040
2.

Functional loss of ATRX and telomerase activates Alternative Lengthening of Telomeres (ALT)

(Submitter supplied) The presence of ALT is strongly associated with recurrent cancer-specific somatic inactivating mutations in the ATRX-DAXX chromatin remodeling complex. Here, we generate an ALT-positive adenocarcinoma cell line following functional inactivation of ATRX and telomerase in a telomerase-positive carcinoma cell line.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13497
8 Samples
Download data: TXT
Series
Accession:
GSE129448
ID:
200129448
3.

Effect of p53 knockout on gene expression during capmatinib treatment of NF1-MET murine MPNST cells

(Submitter supplied) To investigate the function of p53 in regulating response to MET inhibition in MPNST cells we established NF1-MET;sgP53 cells in which Trp53 was knocked out using CRISPR-Cas9. As a control, the parental NF1-MET was transduced with CRISPR-Cas9 in the absence of sgRNA. We then performed gene expression profiling analysis using data obtained from RNA-seq of the 2 different cells treated with either capmatinib or vehicle in duplicate.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24247
8 Samples
Download data: TXT
Series
Accession:
GSE225747
ID:
200225747
4.

Molecular characterization of a series of 7 NF1-associated human MPNSTs

(Submitter supplied) 7 MPNSTs from 7 neurofibromatosis-type 1 patients were screened with a high resolution array-CGH. Each MPNST DNA (somatic tumor DNA) was individually hybridized on Agilent whole human genome 244K microarrays (Platform GPL4091) using the pooled genomic constitutional DNA (lymphocytes DNA) from the normal control patients as reference, in order to detect tumor-specific aberrations.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL4091
7 Samples
Download data: TXT
Series
Accession:
GSE92647
ID:
200092647
5.

Malignant peripheral nerve sheath tumor (MPNST) and MPNST-like entities defined by DNA methylation profile in pediatric and juvenile population

(Submitter supplied) The diagnosis of Malignant peripheral nerve sheath tumors (MPNSTs) can be challenging, but is aided by their characteristic DNA methylation profile (DMP). An MPNST-like group, characterized by retained H3K27me3 expression, was recently recognized. To evaluate the diagnostic usefulness of DMP in pediatric/juvenile MPNSTs, we selected pediatric/juvenile malignancies from the Bambino Gesù Children's Hospital DMP database. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL21145
42 Samples
Download data: IDAT
Series
Accession:
GSE246644
ID:
200246644
6.

Epigenomic reprogramming due to PRC2 functional loss induces an aggressive de-differentiated neural crest-like phenotype in MPNST

(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:
GPL20301 GPL11154
126 Samples
Download data: BED, BROADPEAK, BW, TAB
Series
Accession:
GSE141439
ID:
200141439
7.

RNA-seq dataset for MPNST patient tissue samples

(Submitter supplied) Comprehensive transcriptomic profiling of PRC2 mutant MPNST patient tissues with adjacent normal tissues and neurofibroma patient tissues was performed to investigate gain of specific transcriptional signature associated with PRC2 loss during transformation to MPNST.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
17 Samples
Download data: TAB, TXT
Series
Accession:
GSE141438
ID:
200141438
8.

RNA-seq dataset for MPNST cell lines

(Submitter supplied) Comprehensive transcriptomic profiling of PRC2 mutant and WT MPNST cell lines were performed to investigate PRC2-dependent transcriptional programs that are activated due to PRC2 loss
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20301
39 Samples
Download data: TAB, TXT
Series
Accession:
GSE141437
ID:
200141437
9.

ChIP-seq dataset for epigenomic landscape of MPNST

(Submitter supplied) In order to comprehensively define the epigenetic patterns specific to MPNST, we generated profiles for 6 histone modification marks, including H3K4me1 (enhancer), H3K27Ac (active enhancer), H3K9me3 (heterochromatin), H3K27me3 (polycomb repression), H3K79me2 (transcription) and H3K4me3 (promoter). Systematic epigenomic profiling of chromatin states in MPNST cells revealed epigenetic subtypes in MPNST based on Polycomb related repressive and bivalent chromatin states. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
70 Samples
Download data: BED, BROADPEAK, BW
Series
Accession:
GSE141435
ID:
200141435
10.

PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies [expression array]

(Submitter supplied) The polycomb repressive complex 2 (PRC2) exerts oncogenic effects in many tumour types1. However, loss-of-function mutations in PRC2 components occur in a subset of haematopoietic malignancies, sug- gesting that this complex plays a dichotomous and poorly understood role in cancer2,3. Here we provide genomic, cellular, and mouse mod- elling data demonstrating that the polycomb group gene SUZ12 func- tions as tumour suppressor in PNS tumours, high-grade gliomas and melanomas by cooperating with mutations in NF1. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
9 Samples
Download data: CEL
Series
Accession:
GSE62500
ID:
200062500
11.

PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies [ChIP-seq]

(Submitter supplied) The polycomb repressive complex 2 (PRC2) exerts oncogenic effects in many tumour types1. However, loss-of-function mutations in PRC2 components occur in a subset of haematopoietic malignancies, suggesting that this complex plays a dichotomous and poorly understood role in cancer2,3. Here we provide genomic, cellular, and mouse mod- elling data demonstrating that the polycomb group gene SUZ12 func- tions as tumour suppressor in PNS tumours, high-grade gliomas and melanomas by cooperating with mutations in NF1. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT
Series
Accession:
GSE62499
ID:
200062499
12.

PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11154 GPL6244
15 Samples
Download data: CEL, TXT
Series
Accession:
GSE52777
ID:
200052777
13.

Epigenomic analysis of Atrx deficiency in murine glioma cells of orgin

(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
50 Samples
Download data: BED, TXT, WIG
Series
Accession:
GSE100465
ID:
200100465
14.

Epigenomic analysis of Atrx deficiency in murine glioma cells of orgin [RNA-seq]

(Submitter supplied) The chromatin regulator ATRX is inactivated in large subsets of adult and pediatric glioma. Whether and how ATRX deficiency promotes oncogenesis by epigenomic dysregulation remains unclear. We found that Atrx loss, especially when coupled with Tp53 inactivation, promoted cell motility and modulated differentiation state in primary murine neuroepithelial progenitors, recapitulating characteristic disease phenotypes and molecular features. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17021
12 Samples
Download data: TXT
Series
Accession:
GSE100464
ID:
200100464
15.

Epigenomic analysis of Atrx deficiency in murine glioma cells of orgin [H3.3 ChIP]

(Submitter supplied) The chromatin regulator ATRX is inactivated in large subsets of adult and pediatric glioma. Whether and how ATRX deficiency promotes oncogenesis by epigenomic dysregulation remains unclear. We found that Atrx loss, especially when coupled with Tp53 inactivation, promoted cell motility and modulated differentiation state in primary murine neuroepithelial progenitors, recapitulating characteristic disease phenotypes and molecular features. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
18 Samples
Download data: BROADPEAK
Series
Accession:
GSE100463
ID:
200100463
16.

Epigenomic analysis of Atrx deficiency in murine glioma cells of orgin [Atrx ChIP]

(Submitter supplied) The chromatin regulator ATRX is inactivated in large subsets of adult and pediatric glioma. Whether and how ATRX deficiency promotes oncogenesis by epigenomic dysregulation remains unclear. We found that Atrx loss, especially when coupled with Tp53 inactivation, promoted cell motility and modulated differentiation state in primary murine neuroepithelial progenitors, recapitulating characteristic disease phenotypes and molecular features. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
14 Samples
Download data: BED
Series
Accession:
GSE100462
ID:
200100462
17.

Epigenomic analysis of Atrx deficiency in murine glioma cells of orgin [ATAC-seq]

(Submitter supplied) The chromatin regulator ATRX is inactivated in large subsets of adult and pediatric glioma. Whether and how ATRX deficiency promotes oncogenesis by epigenomic dysregulation remains unclear. We found that Atrx loss, especially when coupled with Tp53 inactivation, promoted cell motility and modulated differentiation state in primary murine neuroepithelial progenitors, recapitulating characteristic disease phenotypes and molecular features. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL17021
6 Samples
Download data: BED, WIG
Series
Accession:
GSE100461
ID:
200100461
18.

Gene profiles of pathway interference downstream neurofibromin signaling

(Submitter supplied) Malignant peripheral nerve sheath tumor (MPNST) is a type of soft tissue sarcoma that occurs in carriers of mutations in the neurofibromatosis type I gene (Nf1) as well as sporadically. Plexiform neurofibromas in NF1 patients have a significant risk of developing into MPNSTs leading to increased morbidity and mortality from this syndrome. Surgery is the primary intervention but it is not always effective due to the tendency of MPNSTs to infiltrate the surrounding tissue or grow in an inoperable location. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
24 Samples
Download data: TXT
Series
Accession:
GSE39764
ID:
200039764
19.

Highly Aneuploid Zebrafish Malignant Peripheral Nerve Sheath Tumors have Genetic Alterations Similar to Human Cancers

(Submitter supplied) Aneuploidy is a hallmark of human cancers, but most mouse cancer models lack the extensive aneuploidy seen in many human tumors. The zebrafish is becoming an increasingly popular model for studying cancer. Here we report that malignant peripheral nerve sheath tumors (MPNSTs) that arise in zebrafish as a result of mutations in either ribosomal protein (rp) genes or in p53 are highly aneuploid. Karyotyping reveals that these tumors frequently harbor near-triploid numbers of chromosomes, and they vary in chromosome number from cell-to-cell within a single tumor. more...
Organism:
Danio rerio
Type:
Genome variation profiling by array; Genome variation profiling by high throughput sequencing
Platforms:
GPL10797 GPL9319
48 Samples
Download data: TXT
20.

MIT-KI zebrafish Zv7+8 15K CGH v1.0

(Submitter supplied) This genomic 15K CGH array was custom designed against zebrafish (Danio rerio) genome assembly danRef5/Zv7 (available at: http://hgdownload.cse.ucsc.edu/goldenPath/danRer5/bigZips/) on the basis of a database of seven million genomic probe sequences provided by Agilent. Probe sequences were later re-mapped with respect to genome assembly danRer6/Zv8 (http://hgdownload.cse.ucsc.edu/goldenPath/danRer6/bigZips/). more...
Organism:
Danio rerio
1 Series
42 Samples
Download data
Platform
Accession:
GPL10797
ID:
100010797
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