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Links from GEO DataSets

Items: 18

1.
Full record GDS3634

miR-205 expression effect on prostate cancer cell line

Analysis of DU145 prostate cancer cells with restored miR-205 expression. miR-205 expression is lower in prostate cancer cell lines than in normal cell lines, as well as in prostate tumors than in matched normal prostate tissues. Results provide insight into the role of miR-205 in prostate cancer.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 protocol sets
Platform:
GPL6104
Series:
GSE11701
8 Samples
Download data: TXT
DataSet
Accession:
GDS3634
ID:
3634
2.

Genes modulated by miR-205 in DU145 prostate cancer cells

(Submitter supplied) The study was aimed at identifying genes directly or indirectly regulated by miR-205 in the prostate. To this purpose, DU145 prostate cancer cells, which express miR-205 at very low levels, were transfected with miR-205 synthetic precursor and consequent alterations of gene expression analyzed using a microarray approach. Keywords: comparison betweed cells exposed to different miRNA precursors
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS3634
Platform:
GPL6104
8 Samples
Download data: TXT
Series
Accession:
GSE11701
ID:
200011701
3.

Genes regulated by has-mir-31 in glioma cell line

(Submitter supplied) Overexpression of miR-31 inhibits the migration and invasion ability of glioma cell. We sought to obtain the genes regulated by mir-31 in glioma cell line.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
2 Samples
Download data: CEL
Series
Accession:
GSE28810
ID:
200028810
4.

Coordinated regulation of cell cycle transcripts by p53-inducible microRNAs, miR -192 and -215

(Submitter supplied) Cell cycle arrest in response to DNA damage is an important anti-tumorigenic mechanism. microRNAs (miRNAs) were shown recently to play key regulatory roles in cell cycle progression. For example, miR-34a is induced in response to p53 activation and mediates G1 arrest by down-regulating multiple cell cycle-related transcripts. Here we show that genotoxic stress promotes the p53-dependent up-regulation of the homologous miRNAs, miR -192 and miR-215. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4372
6 Samples
Download data
Series
Accession:
GSE13105
ID:
200013105
5.

Identification of miR-145 or miR-133a target genes in squamous cell carcinoma

(Submitter supplied) We recently identified a subset of down-regulated miRNAs such as miR-145 and miR-133a in squamous cell carcinoma. Cell growth inhibitions occurred in miR-145 and miR-133a transfectants compared with the controls, suggesting that both miRNAs function as tumor suppressors. The aims of our expression studies were identification of these miRNAs target genes.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
4 Samples
Download data: TXT
Series
Accession:
GSE20028
ID:
200020028
6.

Identification of miR-145 or miR-133a target genes in bladder cancer

(Submitter supplied) We recently identified a subset of down-regulated miRNAs such as miR-145 and miR-133a in bladder cancer. Cell growth inhibitions occurred in miR-145 and miR-133a transfectants compared with the controls, suggesting that both miRNAs function as tumor suppressors. The aims of our expression studies were identification of these miRNAs target genes.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
4 Samples
Download data: TXT
Series
Accession:
GSE19717
ID:
200019717
7.

Characterization of B- and T-lineage ALL by Integrated Analysis of microRNA and mRNA Expression Profiles

(Submitter supplied) Acute lymphoblastic leukemia (ALL) is an heterogeneous disease comprising several subentities that differ for both immunophenotypic and molecular characteristics. Over the years, the biologic understanding of this neoplasm has largely increased. Gene expression profiling has recently allowed to identify specific signatures for the different ALL subsets and permitted identification of pathways deregulated by a given lesion. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL570 GPL8191
39 Samples
Download data: CEL, XLS
Series
Accession:
GSE14834
ID:
200014834
8.

Genomic Pathways of 17-beta-Estradiol Induced Malignant Cell Transformation in Human Breast Epithelial Cells

(Submitter supplied) The estrogen-dependence of breast cancer has long been recognized, however, the role of 17β-estradiol (E2) in cancer initiation was not known until we demonstrated that it induces complete neoplastic transformation of the human breast epithelial cells MCF-10F. E2-treatment of MCF-10F cells progressively induced high colony efficiency and loss of ductulogenesis in early transformed (trMCF) cells and invasiveness in Matrigel invasion chambers. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE5116
ID:
200005116
9.

Expression data from p63 siRNA in squamous cell lines

(Submitter supplied) p63, a homologue of the tumor suppressor p53, is critical for the development and maintenance of squamous epithelia. p63 is specifically expressed in the basal layers of stratified epithelial tissues, and is considered to be a specific marker for cells of this type. The role of p63 in tumorigenesis remains poorly defined. Numerous studies have highlighted the oncogenic potential of the predominant p63 isoform, ΔNp63α; however, data suggests that other p63 proteins can act as tumor suppressors or alter the metastatic potential of tumors. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS2086 GDS2087 GDS2088
Platforms:
GPL96 GPL97 GPL570
14 Samples
Download data
Series
Accession:
GSE4975
ID:
200004975
10.
Full record GDS2088

Transcription factor p63 inactivation effect on squamous cells (HG-U133 2.0)

Analysis of squamous cell lines following siRNA knockdown of the transcription factor p63, a homolog of the tumor suppressor p53. p63 encodes multiple isoforms that activate or repress transcription, and is critical for the development and maintenance of squamous epithelia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 cell line, 2 cell type, 2 protocol sets
Platform:
GPL570
Series:
GSE4975
6 Samples
Download data
DataSet
Accession:
GDS2088
ID:
2088
11.
Full record GDS2087

Transcription factor p63 inactivation effect on squamous cells (HG-U133B)

Analysis of squamous cells following siRNA knockdown of the transcription factor p63, a homolog of the tumor suppressor p53. p63 encodes multiple isoforms that activate or repress transcription, and is critical for the development and maintenance of squamous epithelia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 cell line, 2 cell type, 2 protocol sets
Platform:
GPL97
Series:
GSE4975
4 Samples
Download data
DataSet
Accession:
GDS2087
ID:
2087
12.
Full record GDS2086

Transcription factor p63 inactivation effect on squamous cells (HG-U133A)

Analysis of squamous cells following siRNA knockdown of the transcription factor p63, a homolog of the tumor suppressor p53. p63 encodes multiple isoforms that activate or repress transcription, and is critical for the development and maintenance of squamous epithelia.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 cell line, 2 cell type, 2 protocol sets
Platform:
GPL96
Series:
GSE4975
4 Samples
Download data
DataSet
Accession:
GDS2086
ID:
2086
13.

Identification of target genes of cancer-related microRNAs in human cancer

(Submitter supplied) To identify target genes of cancer-related microRNAs in human cancer, several cell lines (bladder cancer, prostate cancer, renal cell carcinoma, esophageal squamous cell carcinoma, and head and neck squamous cell carcinoma) were subjected to Agilent whole genome microarrays.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL10332 GPL13607
35 Samples
Download data: TXT
Series
Accession:
GSE37119
ID:
200037119
14.

Genome-wide location map of Polycomb in prostate cancer

(Submitter supplied) We used chromatin immunoprecipitation (ChIP) in combination with human promoter microarrays to idnetify SUZ12 and H3K27me3-occupied gene promoters in prostate cancer cells and tissues. We observed a common set of SUZ12 and H3K27me3-occupied genes in LNCaP cells, and metastatic prostate cancer tissues across individuals as well as tissue types of the metastatic sites. We also found significant overlap of cancer polycomb targets with previously published embryonic stem cell polycomb targets. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
4 related Platforms
14 Samples
Download data: TXT
Series
Accession:
GSE9069
ID:
200009069
15.

Comparison of microRNA expression between prostate adenocarcinoma cells, DU-145 and immortalized normal cells, PWR-1E

(Submitter supplied) The primary goal of this experiment was to determine the endogenous miRNA that are differentially expressed between prostate adenocarcinoma cells, DU-145 and prostate immortalized epithelial cells, PWR-1E. Subsequently, we performed other analysis with BLAST and in silico algorithm searches to determine the appropriate miRNA that could regulate a novel gene MIEN1.
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL19283
2 Samples
Download data: TXT
Series
Accession:
GSE62286
ID:
200062286
16.

Genome-wide analysis of gene expression in EMT cells induced by overexpression of PDGF-D compared with PC3 control cells

(Submitter supplied) Analysis of EMTrelated gene expression levels. The hypothesis tested in the present study was that expression of mesenchymal markers was increased and expression of epithelial markers was downregulated concomitant with increased expression of stem -like cell markers in EMT cells compared with control cells. Results demostrated that overexpression of PDGF-D induced genome-wide gene expression changes which were consistent with EMT phenotype and stem cell signatures.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6884
6 Samples
Download data: TXT
Series
Accession:
GSE22764
ID:
200022764
17.

The RNA-Seq transcriptome of human prostate cancer cell line depleted of CIC

(Submitter supplied) To identify which genes were regulated by CIC in human prostate cancer cell, the effect of CIC knockdown on PC3 cell transcriptome was determined
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10999
4 Samples
Download data: DIFF
18.

Genomic profiling of microRNA and messenger RNA reveals deregulated microRNA expression in prostate cancer.

(Submitter supplied) MicroRNAs are small non-coding RNAs that regulate mRNA function. Recent studies have shown that microRNA expression is altered in tumors. We studied the expression of both microRNAs and mRNAs in 60 primary prostate tumors and 16 non-tumor prostate tissues to evaluate the involvement of microRNAs in prostate cancer. Global microRNA expression was determined in RNA isolated from fresh-frozen human tissues with a custom oligonucleotide microarray chip. more...
Organism:
Mus musculus; Homo sapiens
Type:
Non-coding RNA profiling by array
Platform:
GPL5180
76 Samples
Download data: GPR
Series
Accession:
GSE8126
ID:
200008126
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