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Links from GEO DataSets

Items: 20

1.

Single-cell analysis of gene expression variation and phenotype switching in melanoma

(Submitter supplied) We combine extensive profiling of single-cell gene expression (scRNA-seq of 39,263 cells) and chromatin accessibility applied to ten genetically-homogeneous, patient-derived melanoma cultures, to examine intra- and intertumoral phenotypic heterogeneity, to identify new cell states, and to track dynamic transitions at single-cell resolution.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
4 related Platforms
94 Samples
Download data: BW, TSV
Series
Accession:
GSE134432
ID:
200134432
2.

Decoding the regulatory landscape of melanoma reveals TEADS as regulators of the invasive cell state.

(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
Platform:
GPL11154
52 Samples
Download data: BW, TXT
Series
Accession:
GSE60666
ID:
200060666
3.

Decoding the regulatory landscape of melanoma reveals TEADS as regulators of the invasive cell state.

(Submitter supplied) Understanding the molecular processes underlying intra-tumor heterogeneity is of critical importance to improve the efficiency of therapy and overcome drug resistance. In malignant melanoma, heterogeneity is though to arise -at least partly- through epigenetic rather than genetic reprogramming of proliferating cells, leading to the appearance within the primary tumors of a phenotypically distinct invasive cell subpopulation. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
11 Samples
Download data: BW
Series
Accession:
GSE60665
ID:
200060665
4.

Decoding the regulatory landscape of melanoma reveals TEADS as regulators of the invasive cell state.

(Submitter supplied) Understanding the molecular processes underlying intra-tumor heterogeneity is of critical importance to improve the efficiency of therapy and overcome drug resistance. In malignant melanoma, heterogeneity is though to arise -at least partly- through epigenetic rather than genetic reprogramming of proliferating cells, leading to the appearance within the primary tumors of a phenotypically distinct invasive cell subpopulation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
17 Samples
Download data: TXT
5.

Decoding the regulatory landscape of melanoma reveals TEADS as regulators of the invasive cell state.

(Submitter supplied) Understanding the molecular processes underlying intra-tumor heterogeneity is of critical importance to improve the efficiency of therapy and overcome drug resistance. In malignant melanoma, heterogeneity is though to arise -at least partly- through epigenetic rather than genetic reprogramming of proliferating cells, leading to the appearance within the primary tumors of a phenotypically distinct invasive cell subpopulation. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
24 Samples
Download data: BW
Series
Accession:
GSE60663
ID:
200060663
6.

BORIS/CTCFL-mediated chromatin accessibility alterations promote a pro-invasive transcriptional signature in melanoma cells

(Submitter supplied) Melanoma is the deadliest form of skin cancer, due to its tendency to metastasize early. Brother of Regulator of Imprinted Sites (BORIS), also known as CCCTC binding factor-Like (CTCFL), is a transcription regulator that becomes ectopically expressed in melanoma. We recently showed that BORIS contributes to melanoma phenotype switching by altering the gene expression program of proliferative melanoma cells in favor of a more invasive phenotype. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20301
8 Samples
Download data: NARROWPEAK, XLS
Series
Accession:
GSE211800
ID:
200211800
7.

Sox10 controls migration of melanoma cells through multiple regulatory target genes

(Submitter supplied) It is believed that the inherent differentiation program of melanocytes during embryogenesis predisposes melanoma cells to high frequency of metastasis. Sox10, a transcription factor expressed in neural crest stem cells and a subset of progeny lineages, plays a key role in the development of melanocytes. We show that B16F10 melanoma cells transfected with siRNA specific for Sox10 display reduced migratory activity which in turn indicated that a subset of transcriptional regulatory target genes of Sox10 are likely to be involved in migration and metastasis of melanoma cells. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6238
6 Samples
Download data: TXT
Series
Accession:
GSE25501
ID:
200025501
8.

Expression profiling of WM9 and 1205Lu with shILEI.

(Submitter supplied) We have used lentiviral shRNA vectors to generate pools of melanoma cells (1205Lu and WM9) stably knocked down for ILEI (FAM3C).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15207
18 Samples
Download data: CEL
Series
Accession:
GSE95509
ID:
200095509
9.

Gene expression profiling of 1205Lu human melanoma cells after reversible shifting between monolayer and stem cell-like growth

(Submitter supplied) RNA samples were prepared from a 1205Lu original cell monolayer (OM), melanoma stem cell-like bodies (MB), and a new cell monolayer derived from stem cell-like bodies (NM).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
3 Samples
Download data: TXT
Series
Accession:
GSE62849
ID:
200062849
10.

The transcriptome of a murine model of melanoma initiation and progression unravels molecular signatures of phenotype switch and novel independent prognostic factors for melanoma patients

(Submitter supplied) Despite advances in therapeutics, the progression of melanoma to metastasis still confers a poor outcome to patients. Nevertheless, there is a lack of biological models to understand cellular and molecular changes taking place along disease progression. Here, we analyzed the transcriptome of a multi-stage murine model of melanoma progression comprising a non-tumorigenic melanocyte lineage (melan-a), pre-malignant melanocytes (4C), non-metastatic (4C11-) and metastasis-prone (4C11+) melanoma cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18480
11 Samples
Download data: TXT
Series
Accession:
GSE149884
ID:
200149884
11.

Analysis of long and short enhancers in melanoma cell states

(Submitter supplied) Understanding how enhancers drive cell type specificity and efficiently identifying them is essential for the development of innovative therapeutic strategies. In melanoma, the melanocytic (MEL) and the mesenchymal-like (MES) states present themselves with different responses to therapy, making the identification of specific enhancers highly relevant. Using massively parallel reporter assay (MPRA) in a panel of patient-derived melanoma lines (MM lines), we set to identify and decipher melanoma enhancers by first focusing on regions with state specific H3K27 acetylation close to differentially expressed genes. more...
Organism:
Homo sapiens; synthetic construct
Type:
Other
6 related Platforms
112 Samples
Download data: TSV
Series
Accession:
GSE180879
ID:
200180879
12.

Oncogenic BRAFV600E remodels the melanocyte transcriptome and induces BANCR to regulate melanoma cell migration

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing; Expression profiling by array
Platforms:
GPL570 GPL11154
7 Samples
Download data: BW, CEL, GTF
Series
Accession:
GSE37169
ID:
200037169
13.

Oncogenic BRAFV600E remodels the melanocyte transcriptome and induces BANCR to regulate melanoma cell migration [Affymetrix]

(Submitter supplied) Most cancer genomics papers to date have focused on aberrations in genomic DNA and protein-coding transcripts. However, around 50% of transcripts have no coding potential and may exist as non-coding RNA. We performed RNA-seq in BRAFv600e melanoma skin cancer and on melanocytes over-expressing oncogenic BRAF to catalog transcriptome remodeling. We discovered that BRAF regulates expression of 1027 protein coding transcripts, 39 annotated lncRNAs and 70 novel transcripts. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
3 Samples
Download data: CEL
Series
Accession:
GSE37132
ID:
200037132
14.

Oncogenic BRAFV600E remodels the melanocyte transcriptome and induces BANCR to regulate melanoma cell migration [HT-seq]

(Submitter supplied) Most cancer genomics papers to date have focused on aberrations in genomic DNA and protein-coding transcripts. However, around 50% of transcripts have no coding potential and may exist as non-coding RNA. We performed RNA-seq in BRAFv600e melanoma skin cancer and on melanocytes over-expressing oncogenic BRAF to catalog transcriptome remodeling. We discovered that BRAF regulates expression of 1027 protein coding transcripts, 39 annotated lncRNAs and 70 novel transcripts. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL11154
4 Samples
Download data: BW, GTF
15.

Expression data from melanoma cells grown under neural crest cell culture conditions (spheroid cells) versus under classical adherent conditions (adherent cells) - 2 different specimens of melanoma tumors

(Submitter supplied) Summary: Melanoma spheroids grown under neural crest cell conditions are highly plastic migratory/invasive tumor cells endowed with immunomodulator function Background: The aggressiveness of melanoma tumors is likely to rely on their well-recognized heterogeneity and plasticity. Melanoma comprises multi subpopulations of cancer cells some of which may possess stem cell-like properties supporting the notion of plasticity. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
12 Samples
Download data: CEL
Series
Accession:
GSE26980
ID:
200026980
16.

Hierarchy of TGFβ/SMAD, Hippo/YAP/TAZ and Wnt/β-catenin signaling in melanoma phenotype switching

(Submitter supplied) In melanoma, a switch from a proliferative melanocytic to an invasive mesenchymal phenotype is based on dramatic transcriptional reprogramming which involves complex interactions between a variety of signaling pathways and their downstream transcriptional regulators. TGFb/SMAD, Hippo/YAP/TAZ and Wnt/b-catenin signaling pathways are major inducers of transcriptional reprogramming and converge at several levels. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
36 Samples
Download data: TXT
17.

Gene expression profile in MCF7 breast cancer cells after 78 functionallly important molecules were knocked down using siRNA.

(Submitter supplied) Affymetrix microarray data was generated from MCF7 breast cancer cells treated in vitro with siRNAs against 78 transcription factors and signalling molecules.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
89 Samples
Download data: CEL
Series
Accession:
GSE31912
ID:
200031912
18.

Gene expression profile in A375 melanoma cells after 45 functionally important molecules were knocked down using siRNA

(Submitter supplied) Affymetrix microarray data were generated from A375 melanoma cells treated in vitro with siRNAs against 45 transcription factors and signalling molecules.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4813
Platform:
GPL570
51 Samples
Download data: CEL
Series
Accession:
GSE31534
ID:
200031534
19.
Full record GDS4813

Melanoma cell line response to the depletion of various transcription factors and signaling proteins

Analysis of cultured A375 melanoma cells depleted for various transcription factors and signaling proteins. Results provide insight into the molecular pathogenesis of melanoma.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 47 agent sets
Platform:
GPL570
Series:
GSE31534
51 Samples
Download data: CEL
20.

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
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