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Links from GEO DataSets

Items: 20

1.

Gene expression analysis on ganglia derived from TH-MYCN mice

(Submitter supplied) Amplification of the MYCN oncogene predicts treatment resistance in childhood neuroblastoma. Using a MYC target gene signature that predicts poor neuroblastoma prognosis we identified the histone chaperone, FAcilitates Chromatin Transcription (FACT), as a crucial mediator of the MYC signal and a therapeutic target in the disease. FACT and MYCN expression created a forward feedback loop in neuroblastoma cells that was essential for maintaining mutual high expression. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
13 Samples
Download data: TXT
Series
Accession:
GSE71105
ID:
200071105
2.

Gene expression analysis of BE(2)C cells treated with SSRP1 and MYCN siRNAs

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL16686 GPL10787
21 Samples
Download data: CEL, TXT
Series
Accession:
GSE71062
ID:
200071062
3.

Gene expression analysis of BE(2)C cells treated with MYCN siRNA (MYCN2 #SI03113670)

(Submitter supplied) Amplification of the MYCN oncogene predicts treatment resistance in childhood neuroblastoma. Using a MYC target gene signature that predicts poor neuroblastoma prognosis we identified the histone chaperone, FAcilitates Chromatin Transcription (FACT), as a crucial mediator of the MYC signal and a therapeutic target in the disease. FACT and MYCN expression created a forward feedback loop in neuroblastoma cells that was essential for maintaining mutual high expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
2 Samples
Download data: CEL
Series
Accession:
GSE71061
ID:
200071061
4.

Gene expression analysis of BE(2)C cells treated with MYCN siRNA (MYCN1 #SI03087518)

(Submitter supplied) Amplification of the MYCN oncogene predicts treatment resistance in childhood neuroblastoma. Using a MYC target gene signature that predicts poor neuroblastoma prognosis we identified the histone chaperone, FAcilitates Chromatin Transcription (FACT), as a crucial mediator of the MYC signal and a therapeutic target in the disease. FACT and MYCN expression created a forward feedback loop in neuroblastoma cells that was essential for maintaining mutual high expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
2 Samples
Download data: CEL
Series
Accession:
GSE71060
ID:
200071060
5.

Gene expression analysis of BE(2)C cells treated with SSRP1 siRNA

(Submitter supplied) Amplification of the MYCN oncogene predicts treatment resistance in childhood neuroblastoma. Using a MYC target gene signature that predicts poor neuroblastoma prognosis we identified the histone chaperone, FAcilitates Chromatin Transcription (FACT), as a crucial mediator of the MYC signal and a therapeutic target in the disease. FACT and MYCN expression created a forward feedback loop in neuroblastoma cells that was essential for maintaining mutual high expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
4 Samples
Download data: CEL
Series
Accession:
GSE71059
ID:
200071059
6.

Effect of CBL0137 on DIPG cells

(Submitter supplied) Diffuse intrinsic pontine glioma (DIPG) is an aggressive and incurable childhood brain tumor for which new treatments are needed. A high throughput drug screen of 3600 pharmaceutical compounds found that anti-malarials, including quinacrine had potent activity against DIPG neurospheres. CBL0137 is a novel anti-cancer compound developed from quinacrine, which targets Facilitates Chromatin Transcription (FACT), a chromatin remodelling complex involved in transcription, replication, and DNA repair. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL28835
6 Samples
Download data: CEL
Series
Accession:
GSE153883
ID:
200153883
7.

Combination of CBL0137 and Panobinostat in DIPG

(Submitter supplied) Diffuse intrinsic pontine glioma (DIPG) is an aggressive and incurable childhood brain tumor for which new treatments are needed. A high throughput drug screen of 3600 pharmaceutical compounds found that anti-malarials, including quinacrine had potent activity against DIPG neurospheres. CBL0137 is a novel anti-cancer compound developed from quinacrine, which targets Facilitates Chromatin Transcription (FACT), a chromatin remodelling complex involved in transcription, replication, and DNA repair. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL28782
12 Samples
Download data: CEL
Series
Accession:
GSE153441
ID:
200153441
8.

LMO1 Synergizes with MYCN to Promotes Neuroblastoma Initiation and Metastasis

(Submitter supplied) High levels of LMO1 expression synergizes with MYCN to accelerate neuroblastomagenesis, enhance disease penetrance and promote widespread metastasis in zebrafish. Transcriptomic analysis of human neuroblasotma cells with programed expression of LMO1 vs vector control or neuroblastoma cells with differential endogenous LMO1 expression revealed that gene signitures affecting tumor cell-extracellular matrix interaction are significantly associated with high levels of LMO1 expression. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: TXT
9.

An ALYREF-MYCN coactivator complex drives neuroblastoma tumorigenesis through effects on USP3 and MYCN stability

(Submitter supplied) To achieve the very high oncoprotein levels required to drive the malignant state, cancer cells utilise the ubiquitin proteasome system to regulate proteins involved in growth signalling pathways. Here we identify a transcriptional coactivator, ALYREF, expressed from the most common genetic copy number variation in childhood neuroblastoma, chromosome 17q21-ter gain. We show strong co-operativity between ALYREF and MYCN from transgenic models of neuroblastoma in vitro and in vivo. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20795
2 Samples
Download data: BW, TXT
Series
Accession:
GSE150303
ID:
200150303
10.

The new multi-targeted agent Curaxin-137 suppresses mammary tumorigenesis in Her2/neu transgenic mice

(Submitter supplied) Global gene expression profiles in liver and spleen between Curaxin-treated and control mice
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6887
11 Samples
Download data: TXT
Series
Accession:
GSE33285
ID:
200033285
11.

Effect of CBL0137 on nascent transcription in HT1080 cells [RNA-seq]

(Submitter supplied) Small molecule curaxin CBL0137 has broad anti-cancer activity in different preclinical models. It interferes with histone-DNA interactions via binding to DNA without causing DNA damage. It resposents first in class "chromatin damaging" agent without genotoxic properties. Its effect on the transcription in human tumor cells was evaluated. DNA-targeting small molecules are widely used for anticancer therapy based on their ability to induce cell death, presumably via DNA damage. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
4 Samples
Download data: BW, TXT
12.

Effect of DNA bindng small molecules on SSRP1 genomic distribution

(Submitter supplied) Small molecules directly binding DNA in cells destabilized chromatin what is "sensed" by histone chaperone FACT. FACT binds regions with destabilized chromatin via "c-trapping". DNA-targeting small molecules are widely used for anticancer therapy based on their ability to induce cell death, presumably via DNA damage. DNA in the eukaryotic cell is packed into chromatin, a highly-ordered complex of DNA, histones, and non-histone proteins. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
7 Samples
Download data: BED, BW
Series
Accession:
GSE107595
ID:
200107595
13.

Gene expression analysis of Th-MYCN neuroblastoma tumours treated with CBL0137 and panobinostat

(Submitter supplied) The aim of this experiment is to identify the changes in gene expression induced by CBL0137, panobinostat and their combination
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
11 Samples
Download data: TXT
Series
Accession:
GSE151689
ID:
200151689
14.

Effects of MYCN knockdwon on miRNA expression in neuroblastoma cells

(Submitter supplied) Global miRNAs expression profilling of SK-N-BE(2)-C cells after dsRNA-mediated knockdown of MYCN
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: TXT
Series
Accession:
GSE72721
ID:
200072721
15.

Genome-wide mapping of MYCN binding in neuroblastoma cells

(Submitter supplied) To identify the MYCN transcription factor binding sites across the genome, we performed chromatin immunoprecipitation followed by sequencing (ChIP-seq) using anti-MYCN and anti-IgG antibodies on a MYCN-amplified NB cell line, SK-N-BE(2)-C.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
2 Samples
Download data: BED, TXT
Series
Accession:
GSE72640
ID:
200072640
16.

Differential gene expression in neuroblastoma cells after transfection with control siRNA, MYCN siRNA or TFAP4 siRNA.

(Submitter supplied) We analyed the gene expression profiles after knocking down MYCN or TFAP4. Results showed that transcription factor MYCN and TFAP4 commonly regulats a subset of genes that may contribute to neuroblastoma cells proliferation and migration.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
6 Samples
Download data: CEL
Series
Accession:
GSE74626
ID:
200074626
17.

Genome-wide differential gene expression analysis in light or heavy polysomal RNAs of MYCN-amplified neuroblastoma cells after lncNB1 knockdown with siRNAs.

(Submitter supplied) lncNB1 stabilizes N-Myc protein expression through increasing E2F1 translation.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL23159
20 Samples
Download data: CEL
Series
Accession:
GSE132109
ID:
200132109
18.

To identify transcripts that are differentially expressed in the MYCN amplified vs MYCN non-amplified cell lines using Next Generation Sequencing

(Submitter supplied) The aims of this study are to compare transcripts that are differentially expressed in the MYCN amplified compare to the MYCN non-amplified neuroblastoma cell lines, in particular, long non-coding RNAs. Methods: Ribosomal depleted RNAs from six human neuroblastoma cell lines were subjected to deep sequencing, using Illumina Hiseq. Results: We identified 459 transcripts are differentially expressed betweeen the MYCN amplified and the MYCN non-amplified cell lines. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
6 Samples
Download data: XLSX
19.

Genome wide differential gene expression analysis of MYCN-amplified neuroblastoma cells after lncNB1 knockdown with siRNAs

(Submitter supplied) We identified that knocking lncNB1 reduces N-Myc protein stability, therefore, we performed affymetrix micoarray studies to investigate whether it was a direct or indirect effect. lncNB1 stabilizes N-Myc protein expression through activating DEPDC1B gene transcription.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL23159 GPL16686
12 Samples
Download data: CEL, XLSX
Series
Accession:
GSE113998
ID:
200113998
20.

Gene expression profiling of human neuroblastoma cell line SK-N-AS_tetoff_MYCN cultured in the presence (D+) or absence (D-) of 1 µg/ml doxycycline for 6 days

(Submitter supplied) Microarray gene expression profiling reveals that MYCN reprograms cellular metabolism by transcriptional activation of metabolic pathways critical for cancer cell growth and proliferation
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16686
6 Samples
Download data: CEL
Series
Accession:
GSE164309
ID:
200164309
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