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Links from GEO DataSets

Items: 13

1.

Cell-type-specific tumour sensitivity identified with a bromodomain targeting PROTAC in adenoid cystic carcinoma.

(Submitter supplied) Salivary gland adenoid cystic carcinoma (ACC) is a rare malignancy with limited treatment options. The development of novel therapies is hindered by a lack of preclinical models. We have generated several ACC patient-derived xenograft (PDX) lines that retain the physical and genetic properties of the original tumours, including the presence of the common MYB/MYBL1-NFIB translocation. Using these PDXs, we have developed the conditions for the generation of 2D and 3D ACC models that retain MYB expression and can be used for drug studies. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL30173
6 Samples
Download data: TSV
Series
Accession:
GSE237382
ID:
200237382
2.

Xenograft model systems of adenoid cystic carcinoma

(Submitter supplied) Adenoid cystic carcinoma (ACC) is one of the most common malignancies that arise in the salivary glands, with an incidence of 4.5 per 1,000,000. It can also arise in glandular tissue closely related to salivary glands in the lacrimal gland, nasal passages and tracheobronchial tree, as well as in glands of the breast and vulva. At all of these sites, it is characterized by a distinctive histology of basaloid epithelial cells arranged in cribriform or tubular patterns, usually demonstrating abundant hyaline extracellular matrix secretion and some degree of myoepithelial differentiation. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3977
Platform:
GPL570
22 Samples
Download data: CEL
Series
Accession:
GSE28996
ID:
200028996
3.
Full record GDS3977

Adenoid cystic carcinoma xenograft models

Analysis of xenograft tumors derived from clinical samples of adenoid cystic carcinomas (ACC) implanted into immunodeficient nu/nu mice within 36 hrs of tissue being removed from the human subjects. Results provide insight into molecular mechanisms underlying the pathology of ACC.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 13 other, 2 tissue sets
Platform:
GPL570
Series:
GSE28996
22 Samples
Download data: CEL
4.

Expression data of 13 surgical samples of adenoid cystic carcinoma (ACC), 2 ACC xenografts, and 7 normal salivary gland tissues (NSGs)

(Submitter supplied) This experiment investigates differences in global gene expression between ACC and NSG.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
22 Samples
Download data: CEL, CHP
Series
Accession:
GSE88804
ID:
200088804
5.

Expression data after knockdown of MYB-NFIB and IGF1R/INSR inhibition in ACC cells

(Submitter supplied) The MYB-NFIB gene is a driver-mutation in the majority of adenoid cystic carcinomas (ACCs) and believed to control a large number of genes involved in tumorigenesis. This experiment investigates the effects on gene expression after siRNA knock-down of MYB-NFIB and/or inhibition of IGF1R/INSR signaling in ACC cells.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
18 Samples
Download data: CEL, CHP
Series
Accession:
GSE76094
ID:
200076094
6.

Retinoic acid suppresses MYB in adenoid cystic carcinoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL16791
18 Samples
Download data: NARROWPEAK
Series
Accession:
GSE98008
ID:
200098008
7.

Retinoic acid suppresses MYB in adenoid cystic carcinoma [RNA-seq]

(Submitter supplied) Translocations that drive overexpression of the oncogenic transcription factor MYB are molecular hallmarks of adenoid cystic carcinoma (ACC), a malignant salivary gland tumor. Surgical resection, whenever possible, is the standard therapy for ACC, but there are no available therapeutic options available if surgery fails. Here we performed a chemical genetic screen using a zebrafish embryo culture system and identified retinoic acid agonists as potent suppressors of c-myb. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
6 Samples
Download data: XLSX
8.

Retinoic acid suppresses MYB in adenoid cystic carcinoma [ChIP-seq]

(Submitter supplied) Translocations that drive overexpression of the oncogenic transcription factor MYB are molecular hallmarks of adenoid cystic carcinoma (ACC), a malignant salivary gland tumor. Surgical resection, whenever possible, is the standard therapy for ACC, but there are no available therapeutic options available if surgery fails. Here we performed a chemical genetic screen using a zebrafish embryo culture system and identified retinoic acid agonists as potent suppressors of c-myb. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: NARROWPEAK
Series
Accession:
GSE98006
ID:
200098006
9.

Integrated copy number and transcriptomic profiling reveal novel oncogenic drivers and clinically significant biomarkers in adenoid cystic carcinoma

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by genome tiling array
Platforms:
GPL10123 GPL4091 GPL6244
137 Samples
Download data: CEL, CHP, TXT
Series
Accession:
GSE153230
ID:
200153230
10.

Integrated copy number and transcriptomic profiling reveal novel oncogenic drivers and clinically significant biomarkers in adenoid cystic carcinoma [Agilent]

(Submitter supplied) We analyzed 100 patient samples by high-resolution arrayCGH to study genomic imbalances in ACC.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platforms:
GPL10123 GPL4091
100 Samples
Download data: TXT
Series
Accession:
GSE153228
ID:
200153228
11.

Integrated copy number and transcriptomic profiling reveal novel oncogenic drivers and clinically significant biomarkers in adenoid cystic carcinoma [Affymetrix]

(Submitter supplied) This experiment investigates global gene expression in adenoid cystic carcinoma (30) and normal salivary gland tissue (7).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6244
37 Samples
Download data: CEL, CHP
Series
Accession:
GSE153002
ID:
200153002
12.

An oncogenic MYB feedback loop drives alternate cell fates in adenoid cystic carcinoma

(Submitter supplied) Translocation events are frequent in cancer and may create chimeric fusions or ‘regulatory rearrangements’ that drive oncogene overexpression. Here we identify super-enhancer translocations that drive overexpression of the oncogenic transcription factor MYB as a recurrent theme in adenoid cystic carcinoma (ACC). Whole-genome sequencing data and chromatin maps reveal distinct chromosomal rearrangements that juxtapose super-enhancers to the MYB locus. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16791 GPL15520 GPL18573
46 Samples
Download data: BED, TDF
Series
Accession:
GSE76465
ID:
200076465
13.

Single cell RNA-sequencing identifies a paracrine interaction that may drive oncogenic Notch signaling in human adenoid cystic carcinoma

(Submitter supplied) Salivary adenoid cystic carcinoma (ACC) is a rare but biologically unique biphasic tumor, consisting of malignant myoepithelial and luminal epithelial cells. MYB and Notch signaling have been implicated in the pathophysiology of these tumors, but in vivo descriptions of these two programs in human tumors and investigation into their active coordination remain incomplete. We utilized single cell RNA-sequencing to profile human head and neck ACC, including the first comparison of primary ACC with a matched local recurrence. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
25 Samples
Download data: TXT
Series
Accession:
GSE210171
ID:
200210171
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