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Links from GEO DataSets

Items: 20

1.
Full record GDS4281

Uveal melanoma

Analysis of 29 uveal melanomas isolated from male and female patients. Uveal melanoma is an aggressive intraocular tumor cancer that metastasizes to the liver in ~50% of patients, with high lethality. Results provide insight into molecular pathways involved in uveal melanoma metastatic progression.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 gender, 2 tissue sets
Platform:
GPL570
Series:
GSE27831
29 Samples
Download data: CEL, CHP
2.

Syntenin-1 is expressed in uveal melanoma and correlates with metastatic progression

(Submitter supplied) Uveal melanoma is an aggressive cancer that metastasizes to the liver in about half of patients, being at that time almost always fatal. Identification of patients at high risk of metastases may provide indication for a frequent follow-up for early detection of metastases and treatment. The analysis of the gene expression profiling of primary human uveal melanomas showed high expression of SDCBP (encoding for syndecan-binding protein-1 or syntenin-1), which appeared higher in patients with recurrence, whereas expression of syndecans was lower and unrelated to progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4281
Platform:
GPL570
29 Samples
Download data: CEL, CHP
Series
Accession:
GSE27831
ID:
200027831
3.

Gene expression changes resulting from the stable loss of BAP1 in uveal melanoma cell lines

(Submitter supplied) Uveal melanoma is a highly aggressive cancer with a strong propensity for metastasis, yet little is known about the biological mechanisms underlying this metastatic potential. We recently showed that most metastasizing uveal melanomas, which exhibit a class 2 gene expression profile, contain inactivating mutations in the tumor suppressor BAP1. The aim of this study was to investigate the role of BAP1 in uveal melanoma progression. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
12 Samples
Download data: TXT
Series
Accession:
GSE48863
ID:
200048863
4.

RNA-seq analysis of uveal melanoma cells and biopsy samples treated with FR900359

(Submitter supplied) Uveal melanoma cell lines and short-term cultures of human uveal melanoma cells from biopsy samples were treated with 100 nM FR900359 or vehicle. RNA-seq was performed.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL16791 GPL24676 GPL21290
34 Samples
Download data: H5, TXT
5.

Expression Data from Uveal Melanoma primary tumors.

(Submitter supplied) A high percentage of uveal melanoma patients develop metastatic tumors that predominately occur in the liver. To identify genes associated with metastasis in this pathology, we studied 63 molecular profiles derived from gene expression microarrays performed from enuceated primary tumors. Metastasis free survival analysis was performed to obtain clinical and genomic variables associated to metastasis occurrence. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
63 Samples
Download data: CEL
Series
Accession:
GSE22138
ID:
200022138
6.

Whole-transcript expression data for uveal melanoma

(Submitter supplied) G protein alpha q and 11 are mutated in 90% of uveal melanoma and they activate the MAPK pathway. Using expression microarray analysis, we identified a unique MEK dependent transcriptional signature with genes that are involved in proliferation and tumor cell invasion.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
29 Samples
Download data: TXT
Series
Accession:
GSE33655
ID:
200033655
7.

Effects of Long-term Serial Passaging on the Characteristics and Properties of Cell Lines Derived From Uveal Melanoma Primary Tumors.

(Submitter supplied) Development of liver metastasis remains the most common cause of mortality in uveal melanoma (UM). Although advances in genomics allowed the direct evaluation of clinical samples of this eye cancer, there is still a need for reliable preclinical models to progress from correlative studies to mechanistic investigations. A few UM cell lines have been characterized, but so far the translation of basic knowledge to the clinic for the treatment of metastatic disease has been incremental at best. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13607
8 Samples
Download data: TXT
Series
Accession:
GSE61228
ID:
200061228
8.

Gene expression profiling of ABCB1 positive and ABCB1 negative OCM1A cells

(Submitter supplied) Gene expression profiling of ABCB1 positive and ABCB1 negative OCM1A cells. ABCB1 is an ATP-dependent transporter efflux pump. OCM1A cell line is derived from uveal melanomas.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
6 Samples
Download data: TXT
Series
Accession:
GSE21425
ID:
200021425
9.

Gene expression profile of non-hepatocyte cells of the liver of wild-type and Alb/MDA-9 mice

(Submitter supplied) We created a mouse line with hepatocyte-specific overexpression of the oncogene MDA-9/SDCBP (Alb/MDA-9). We wanted to check how overexpression of MDA-9 in hepatocytes affect gene expression in surrounding non-parenchymal cells. We isolated non-hepatocyte cells from WT and Alb/MDA-9 mice and performed scRNA-seq in these samples.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
8 Samples
Download data: TAR
Series
Accession:
GSE206096
ID:
200206096
10.

Melanoma Differentiation Associated Gene-9/Syndecan Binding Protein (MDA-9/SDCBP) Promotes Hepatocellular Carcinoma (HCC)

(Submitter supplied) The oncogene Melanoma differentiation associated gene-9/syndecan binding protein (MDA-9/SDCBP) promotes tumorigenesis and metastasis in many cancers. However, the role of MDA-9 in regulating HCC has not been well-studied. To unravel the function of MDA-9 in HCC we generated a transgenic mouse with hepatocyte-specific overexpression of MDA-9 (Alb/MDA-9). Alb/MDA-9 mice demonstrated significantly higher incidence of N-nitrosodiethylamine/phenobarbital-induced HCC compared to WT littermates. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21493
6 Samples
Download data: TAB
Series
Accession:
GSE199175
ID:
200199175
11.

Loss of PRC1 in Uveal melanoma

(Submitter supplied) We demonstrated that loss of Histone 2A Ubiquitination and PRC1 activity drives uveal melanoma progression
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL20301 GPL24676
62 Samples
Download data: TXT
12.

Loss of Polycomb Repressive Complex 1 activity and chromosomal instability drive uveal melanoma progression

(Submitter supplied) Chromosomal instability (CIN) and epigenetic alterations have been implicated in tumor progression and metastasis. Yet, how these two hallmarks of cancer are related remains poorly understood. By integrating genetic, epigenetic, and functional analyses at the single cell level, we show that the progression of uveal melanoma (UM), the most common intraocular primary cancer, is driven by loss of Polycomb Repressive Complex 1 (PRC1) in a subpopulation of tumor cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
7 Samples
Download data: CSV, H5AD
Series
Accession:
GSE160883
ID:
200160883
13.

Single-cell RNA-seq reveals intratumoral heterogeneity in primary uveal melanomas

(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 genome tiling array; Other
Platforms:
GPL18573 GPL10123 GPL11154
18 Samples
Download data: H5, TXT, VCF
Series
Accession:
GSE138665
ID:
200138665
14.

Whole exome sequencing of human primary uveal melanomas

(Submitter supplied) Primary uveal melanomas show multiple genetic alterations. To determine mutational status of six human primary uveal melanomas, we performed whole exome sequencing (WES) and called Single Nucleotide Polimorphism (SNPs) to identify somatic mutations in these human primary uveal melanomas.
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
6 Samples
Download data: VCF
Series
Accession:
GSE138664
ID:
200138664
15.

Single-cell RNA-seq reveals intratumoral heterogeneity in primary uveal melanomas and discloses new targetable vulnerability

(Submitter supplied) Lack of specific markers for invasive uveal melanoma cells prevents early diagnosis of metastasis, while no systemic treatment options are available for patients with disseminated uveal melanomas. Intra-tumor heterogeneity has been recognized in numerous cancers as the main cause of metastasis development and therapy resistance. However, in uveal melanomas the specific subpopulations and their biological function which influence tumor behavior remained unknown. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
6 Samples
Download data: H5
Series
Accession:
GSE138433
ID:
200138433
16.

Array CGH analysis of human uveal melanomas

(Submitter supplied) Primary uveal melanomas show multiple chromosomal aberrations. To identify genome variation in six human primary uveal melanomas, genome wide copy number variation (CNV) analyses were carried out in human primary uveal melanoma samples using array comparative genome hybridization.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL10123
6 Samples
Download data: TXT
Series
Accession:
GSE138404
ID:
200138404
17.

Expression data from normal melanocyte, melanoma cells and their exosomes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; synthetic construct
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL570 GPL8786
15 Samples
Download data: CEL
Series
Accession:
GSE35389
ID:
200035389
18.

Expression data from normal melanocyte, melanoma cells and their exosomes (mRNA)

(Submitter supplied) Exosomes are small membraneous vesicles secreted into body fluids by tumors. Tumor exosomes contain intact and functional mRNAs, small RNAs (including miRNAs), and proteins that can alter the cellular environment to favor tumor growth. Further exploration into the molecular profiling of exosomes may increase our understanding of their roles in melanoma progression in vivo, and may have potential application in biomarker studies. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
8 Samples
Download data: CEL
Series
Accession:
GSE35388
ID:
200035388
19.

Expression data from normal melanocyte, melanoma cells and their exosomes (microRNA)

(Submitter supplied) Exosomes are small membraneous vesicles secreted into body fluids by tumors. Tumor exosomes contain intact and functional mRNAs, small RNAs (including miRNAs), and proteins that can alter the cellular environment to favor tumor growth. Further exploration into the molecular profiling of exosomes may increase our understanding of their roles in melanoma progression in vivo, and may have potential application in biomarker studies. more...
Organism:
synthetic construct; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL8786
7 Samples
Download data: CEL
Series
Accession:
GSE35387
ID:
200035387
20.

Intra- and inter-tumoral heterogeneity of liver metastases in a patient with uveal melanoma

(Submitter supplied) Tumour heterogeneity has been the main obstacle to the clinical efficacy of targeted and immunotherapy in cancer. An accurate understanding and recognition of tumour heterogeneity is critical in the clinical management of cancer patients. Here, we utilised single-cell RNA sequencing (scRNA-seq) to uncover the intra- and inter-tumoural heterogeneity of liver metastases from a patient with metastatic uveal melanoma.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
2 Samples
Download data: MTX, TSV
Series
Accession:
GSE176029
ID:
200176029
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