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Links from GEO DataSets

Items: 20

1.

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
2.

Expression data from normal melanocyte, melanoma cells and their exosomes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
synthetic construct; Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL570 GPL8786
15 Samples
Download data: CEL
Series
Accession:
GSE35389
ID:
200035389
3.

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:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL8786
7 Samples
Download data: CEL
Series
Accession:
GSE35387
ID:
200035387
4.

Differential expression analysis of RNA-seq data from melanocytes driven by tumor cell-derived exosomes

(Submitter supplied) Exosomes (40–100 nm) are organelle-like membranous structures shed into interstitial spaces and body fluids under diverse pathophysiologic conditions, including tumor development. The tumor microenvironment is abundant with exosomes secreted by the cancer cells themselves. Studies have shown that tumor-derived exosomes can transport RNA and active molecules to other cells to promote tumor growth. Exosomes are increasingly being recognized as a major contributor in the progression of malignant neoplasms. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18573
9 Samples
Download data: TXT
5.

miRNA signatures of intracellular and extracellular fractions from cancer cell lines

(Submitter supplied) For the purpose of finding a novel tumor marker, we conducted microRNA profiling analysis in fractions of cells, exosomes, and culture medium from seven cancer cell lines. Ranking data of the intracellular and extracellular microRNAs obtained by microarray analysis, we found that let-7 microRNA family are rich in all fractions from AZ-P7a cells, a metastatic gastric cancer cell line.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL14767
41 Samples
Download data: TXT
Series
Accession:
GSE21350
ID:
200021350
6.

Impact of B16F0 exosomes on the transcriptome of CTLL2 cytotoxic T cells

(Submitter supplied) While recent clinical studies demonstrate the promise of cancer immunotherapy, a barrier for broadening the clinical benefit is identifying how tumors locally suppress cytotoxic immunity. As an emerging mode of intercellular communication, exosomes secreted by malignant cells can deliver a complex payload of coding and non-coding RNA to cells within the tumor microenvironment. Here, we quantified the RNA payload within tumor-derived exosomes and the resulting dynamic transcriptomic response to cytotoxic T cells upon exosome delivery to better understand how tumor-derived exosomes can alter immune cell function. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18480
28 Samples
Download data: CSV
Series
Accession:
GSE103000
ID:
200103000
7.

Analysis of circRNAs expression in melanocytes and melanoma cells

(Submitter supplied) Malignant melanoma (MM) is a highly malignant tumor with poor prognosis. However, the molecular mechanism of melanoma invasion and metastasis remains unclear. In the present study, we performed the profiling of circRNA expression in normal melanocytes and melanoma cells with different invasive abilities using circRNA microarray analysis.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19978
3 Samples
Download data: TXT
Series
Accession:
GSE235561
ID:
200235561
8.

MicroRNA profiling of brain metastasis competent cell-derived exosomes

(Submitter supplied) Objective of this work was to characterize the miRNA profile of exosomes isolated from brain-homing cell lines (MDA-MB-231BR, CTC1BMSM, and 70W) with their respective parental non-brain metastatic cell lines (MDA-MB-231P, CTC1P and MeWo).
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL17456
6 Samples
Download data: TXT
Series
Accession:
GSE48934
ID:
200048934
9.

Comparative microarray analysis of microRNA expression profiles in primary cutaneous malignant melanoma, cutaneous malignant melanoma metastases and benign melanocytic naevi

(Submitter supplied) Perturbations in microRNA (miRNA) expression profiles has been reported for cutaneous malignant melanoma (CMM). With regards to a rapidly growing number of newly discovered miRNA sequences, the availability of up-to-date miRNA expression profiles for primary cutaneous malignant melanoma (PCMM), cutaneous malignant melanoma metastases (CMMM) and benign melanocytic naevi (BMN) is limited. Patients with PCMM (n=9), CMMM (n=4) and BMN (n=8) were included in the study. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL15019
21 Samples
Download data: TXT
Series
Accession:
GSE34460
ID:
200034460
10.

Identification of new markers of cutaneous melanoma invasion

(Submitter supplied) T1C3 is a clonal cell line from a human melanoma tumor, expressing PNA lectin, and characterized by a high capacity of dermal invasion. IC8 is a clonal cell line from a human melanoma tumor, negative for PNA lectin, and non-invasive. To identify new gene markers involved in the mechanisms of early invasion, oligonuclotide microarrays were used to assess transcriptional chnages between the two cell lines.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4803
4 Samples
Download data: GPR
Series
Accession:
GSE15802
ID:
200015802
11.

Solar UVR and exosomal miRNAs effect pre-mature senescence in melanocytes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array; Expression profiling by RT-PCR
Platforms:
GPL21572 GPL24558
10 Samples
Download data: CEL, CHP, SDS
Series
Accession:
GSE141620
ID:
200141620
12.

Solar UVR and exosomal miRNAs effect pre-mature senescence in melanocytes [RT-PCR]

(Submitter supplied) The selection of specific miRNAs by exosomes and their release from cultured melanocytes after exposure to solar UVR (UVA+UVB) have activities in inducing these cells into a premature senescence. In this analysis, human TaqMan microRNA array cards A+B were used to measure the relative expression of miRNAs in exosomes isolated from the irradiated and un-irradiated melanocytes.
Organism:
Homo sapiens
Type:
Expression profiling by RT-PCR
Platform:
GPL24558
8 Samples
Download data: SDS, XLS
Series
Accession:
GSE141619
ID:
200141619
13.

Solar UVR and exosomal miRNAs effect pre-mature senescence in melanocytes [microarray]

(Submitter supplied) The selection of specific miRNAs by exosomes and their release from cultured melanocytes after exposure to solar UVR (UVA+UVB) have activities in inducing these cells into a premature senescence.
Organism:
Homo sapiens; synthetic construct
Type:
Non-coding RNA profiling by array
Platform:
GPL21572
2 Samples
Download data: CEL, CHP
Series
Accession:
GSE141618
ID:
200141618
14.

RNA sequencing in LLCs from co-injected mice or LLC injection alone.

(Submitter supplied) we analyzed transcriptomic profiles in LLC cells isolated from primary cancer sites. C57BL/6 mice were subcutaneously injected with LLC-RFP with or without BMSCs.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL23479
6 Samples
Download data: TXT
Series
Accession:
GSE120349
ID:
200120349
15.

Murine cells: MSC+LLC-serum-exosome vs LLC-serum-exosome

(Submitter supplied) Exosomal miRNAs including 86 exosomal miRNAs were significantly increased and 354 exosomal miRNAs were significantly decreased in the co-injection group compared to LLC injection alone through expression profiling of a total of 1903 genes.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL21265
2 Samples
Download data: TXT
Series
Accession:
GSE119887
ID:
200119887
16.

Murine MSCs: MSC-exosome-hypoxia vs MSC-exosome-normoxia

(Submitter supplied) MiRNA microarray analysis was performed on exosomes secreted by mouse MSC cells under two different conditions of normal oxygen and hypoxia, in order to find out the different miRNAs in exosomes secreted by MSC under two different conditions.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL22383
2 Samples
Download data: TXT
Series
Accession:
GSE119790
ID:
200119790
17.

Identification of functional interactions through integration and systems analysis of matched gene and microRNA expression data across the Ludwig-Melbourne Melanoma (LM-MEL) Cell Line Panel

(Submitter supplied) MicroRNAs contribute to metastatic progression in many cancers by modulation of phenotypic reprogramming processes such as epithelial-mesenchymal plasticity. However, it remains challenging to identify microRNA-mRNA interactions of functional significance at endogenous expression levels. The LM-MEL cell line panel comprises a large set of unique melanoma cell lines derived from largely metastatic melanoma tumours, as described in Behren et al, PCMR 2013 26(4):597-600 (PMID 23527996). more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
57 Samples
Download data: TXT
Series
Accession:
GSE89438
ID:
200089438
18.

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
19.
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
20.

Transcriptome stability profiling using 5'-bromouridine IP chase (BRIC-seq) identifies novel and functional microRNA targets in human melanoma cells.

(Submitter supplied) RNA half-life is closely related to its cellular physiological function, so stability determinants may have regulatory functions. Micro(mi)RNAs have primarily been studied with respect to post-transcriptional mRNA regulation and target degradation. Here we study the impact of the tumour suppressive melanoma miRNA miR-211 on transcriptome stability and phenotype in the non-pigmented melanoma cell line, A375. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
12 Samples
Download data: CSV
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