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Links from GEO DataSets

Items: 20

1.

Aberrant promoter methylation and gene amplification in colorectal cancer

(Submitter supplied) To identify new markers for colorectal cancer we scrutinized the methylation status by methyl-CpG immunoprecipitation followed by global methylation profiling on a CpG island microarray, as altered expression could drive genomic and chromosomal instability observed in these tumors. We show for the first time hypermethylation of MMP9, DNMT3A, and LIG4 in CRC which was confirmed in two independent ethnic CRC patients groups. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL9767
16 Samples
Download data: TXT
Series
Accession:
GSE47413
ID:
200047413
2.

Genes regulated by miR-34b/c and DAC

(Submitter supplied) We found frequent epigenetic silencing of microRNA-34b/c in human colorectal cancer. Introduction of miR-34b/c into a colorectal cancer cell line induced significant changes in gene expression profile. We also found overlap between the genes downregulated by miR-34b/c and those downregulated by DAC. Keywords: dose response
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
5 Samples
Download data: TXT
Series
Accession:
GSE10455
ID:
200010455
3.

Analysis of gene expression in colorectal cancer cells with DGKG overexpression

(Submitter supplied) To clarify the role of diacylglycerol kinase gamma (DGKG) in colorectal cancer, we carried out a gene expression microarray analysis using HCT116 cells infected with adenoviral vectors which express LacZ, kinase-dead mutant of DGKG (DGKG-KD) or constitutively active form of DGKG (DGKG-CA).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13607
3 Samples
Download data: TXT
Series
Accession:
GSE92573
ID:
200092573
4.

Methylation-silenced genes in colorectal cancer cell lines

(Submitter supplied) Using an oligonucleotide array, we undertook a genome-wide search for genes upregulated following treatment with a demethylating agent in two CRC cell lines. Promoter methylation status was determined in 12 CRC cell lines and 11 CRC tissues. After the treatment, 350 genes were upregulated 1.5 fold or more. Six genes (PAGE-5, VCX, MAEL, GAGED2, UCHL1, and GAGE7), which contained putative 5'CpG islands in their promoter regions, were confirmed to be silenced in CRC cell lines. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by array
Platform:
GPL1291
4 Samples
Download data: TXT
Series
Accession:
GSE7687
ID:
200007687
5.

Genome-wide methylation analysis identifies core set of hypermethylated genes in CIMP-H colorectal cancer

(Submitter supplied) DNA methylation was analysed using the Illumina Infinium HumanMethylation 450 Beadchip in 94 matched tissue pairs of colorectal cancer patients.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
192 Samples
Download data: TXT
Series
Accession:
GSE77718
ID:
200077718
6.

Gene expression analysis of colorectal tumors and matched adjacent non-tumor colorectal tissues.

(Submitter supplied) We performed gene expression profiling of 26 colorectal tumors and matched histologically normal adjacent colonic tissue samples using the Illumina Ref-8 whole-genome expression BeadChip. We performed an integrated analysis of promoter DNA methylation and gene expression data to investigate the effects of DNA hypermethylation on gene expression.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6883
52 Samples
Download data: TXT
Series
Accession:
GSE25070
ID:
200025070
7.

Genome-scale analysis of aberrant DNA methylation in colorectal cancer

(Submitter supplied) To characterize DNA methylation-based subgroups in colorectal cancer, we performed genome-scale DNA methylation profiling of 125 colorectal tumor samples and 29 histologically normal-adjacent colonic tissue samples using the Illumina Infinium DNA methylation assay, which assesses the DNA methylation status of 27,578 CpG sites located at the promoter regions of 14,495 protein-coding genes. We identified four DNA methylation-based subgroups of CRC using model-based cluster analyses. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL8490
154 Samples
Download data: TXT
Series
Accession:
GSE25062
ID:
200025062
8.

Analysis of DNA methylation and gene expression in TET1 depleted colorectal cancer cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by genome tiling array
Platforms:
GPL16699 GPL13534
30 Samples
Download data: IDAT, TXT
Series
Accession:
GSE84400
ID:
200084400
9.

Analysis of DNA methylation in TET1 depleted colorectal cancer HCT116 cells

(Submitter supplied) We aimed to analyze the relationship between TET1 and aberrant CpG methylation in colorectal cancer (CRC). We established two stable TET1 knockdown clones and negative control clones of HCT116 cells, and carried out DNA methylation analysis with HumanMethylation450 BeadChip.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
4 Samples
Download data: IDAT, TXT
Series
Accession:
GSE84399
ID:
200084399
10.

Analysis of gene expression in TET1 depleted colorectal cancer HCT116 cells

(Submitter supplied) We aimed to analyze the relationship between TET1 and aberrant CpG methylation in colorectal cancer (CRC). We established two stable TET1 knockdown clones and negative control clones of HCT116 cells, and carried out gene expression analysis with Agilent Human Gene Expression microarray kit.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16699
8 Samples
Download data: TXT
Series
Accession:
GSE84398
ID:
200084398
11.

Analysis of DNA methylation in TET1 depleted colorectal cancer Colo320DM cells

(Submitter supplied) We aimed to analyze the relationship between TET1 and aberrant CpG methylation in colorectal cancer (CRC). We established three stable TET1 knockdown clones and negative control clones of Colo320DM cells, and carried out DNA methylation analysis with HumanMethylation450 BeadChip.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
6 Samples
Download data: IDAT, TXT
Series
Accession:
GSE84397
ID:
200084397
12.

Analysis of gene expression in TET1 depleted colorectal cancer Colo320DM cells

(Submitter supplied) We aimed to analyze the relationship between TET1 and aberrant CpG methylation in colorectal cancer (CRC). We established three stable TET1 knockdown clones and negative control clones of Colo320DM cells, and carried out gene expression analysis with Agilent Human Gene Expression microarray kit.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL16699
12 Samples
Download data: TXT
Series
Accession:
GSE84396
ID:
200084396
13.

Anti-cancer drug sensitive DNA methylation marker research

(Submitter supplied) Genome wide DNA methylation profiling of normal and colon cancer and assosiation study between anti-cancer drug respond group and non-respond group. The Illumina Infinium 27k Human DNA methylation Beadchip v1.2 was used to obtain DNA methylation profiles across approximately 27,000 CpGs in 118 paired anti-cancer drug response tested colon cancer and adjacent normal tissues
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL8490
248 Samples
Download data: TXT
Series
Accession:
GSE27130
ID:
200027130
14.

Expression data from human colonic biopsy samples (adenoma-carcinoma)

(Submitter supplied) Whole genomic microarray analysis was performed in order to identify gene expression profile alterations focusing on the dysplastic adenoma-carcinoma transition. Our aims were to determinate characteristic transcript sets for developing diagnostic mRNA expression patterns for objective classification of benign and malignant colorectal diseases and to test the classificatory power of these markers on an independent sample set.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
94 Samples
Download data: CEL
Series
Accession:
GSE37364
ID:
200037364
15.

Identity of the human cancer cell DNA hypermethylome revealed by gene expression profiling

(Submitter supplied) Altered gene expression is a hallmark of human cancers and arises in part through abnormal epigenetic regulation of gene transcription. The best characterized epigenetic alteration involves tumor suppressor gene inactivation via transcriptional repression associated with aberrant DNA hypermethylation of promoter region CpG islands1. Despite characterization of a growing number of such genes, the majority have yet to be identified. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL1708
10 Samples
Download data: TXT
Series
Accession:
GSE4763
ID:
200004763
16.

Methylome, hydroxymethylome, and integrative transcriptome profiling in human CRC tissue and paired normal tissues

(Submitter supplied) DNA methylation (5-mC) and hydroxymethylation (5-hmC) are regarded as important epigenetic hallmarks in the carcinogenesis of colorectal cancer by transcriptional regulation. 5hmC is an intermediate during active demethylation and maintains the equilibrium of DNA methylation. Previous studies on DNA methylation don’t differentiate 5-hmC from 5-mC. Here, in order to elucidate the epigenetic mechanisms of carcinogenesis of colorectal cancer, we integrate genome wide levels of 5-mC, 5-hmC and Transcriptional expression. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL11154
36 Samples
Download data: TXT, WIG, XML
17.

S100P, a calcium-binding protein, is associated with polypoid tumour growth in colorectal carcinogenesis

(Submitter supplied) Colorectal cancer (CRC) is a genetically heterogeneous disease with several distinct morphological growth patterns. This study was aimed to investigate genes differentially expressed between ulcerative and polypoid colorectal CRC. cDNA microarray was first employed to compare the gene expression profiling of ulcerative and polypoid CRC with paired normal mucosa. Potential candidates identified by data filtering were further validated using quantitative real-time polymerase chain reaction, western blot and immunohistochemistry. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL17157
16 Samples
Download data: GPR
Series
Accession:
GSE46905
ID:
200046905
18.

Genome-wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between CpG methylation and histological subtypes.

(Submitter supplied) Aberrant methylation of DNA is supposed to be a major and early driver of colonic adenoma development and may also lead to colorectal cancer (CRC) formation. While gene methylation assays are used already for CRC screening, differential epigenetic alterations of recurring and non-recurring colorectal adenomas have yet not been systematically investigated. Here, we collected a sample set (n=72) of formalin-fixed paraffin-embedded (FFPE) primary colorectal adenomas without recurrence (n=30), primary adenomas with recurrence at the same location (n=19), so-called “matched pair samples” (n=10; comprising the primary adenoma and the recurrent adenoma) and normal mucosa specimens (n=3). more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
72 Samples
Download data: IDAT, TXT
Series
Accession:
GSE129364
ID:
200129364
19.

Comparative genome-wide DNA methylation analysis of colorectal tumor and matched normal tissues

(Submitter supplied) In our study we applied a genome-wide DNA methylation analysis approach, MethylCap-seq, to map the differentially methylated regions in 24 tumor and matched normal colon samples. In total, 2687 frequently hypermethylated and 468 frequently hypomethylated regions were identified, which include potential biomarkers for CRC diagnosis. Hypermethylation in the tumor samples was enriched at CpG islands and gene promoters, while hypomethylation was distributed throughout the genome. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL10999
68 Samples
Download data: BED, TXT, WIG
20.

DNMT3B targets in RKO cells by ChIP-on-chip

(Submitter supplied) Chromatin immunoprecipitation with DNMT3B specific antibody followed by CGI microarray identified genes with or without CGIs, repeat elements and genomic contigs in RKO cells. ChIP-Chop analysis showed that majority of the target genes including P16, DCC, DISC1, SLIT1, CAVEOLIN1, TBX5, TBX18, HOXB13 and some histone variants, that harbor CGI in their promoters, were methylated in multiple colon cancer cell lines but not in normal colon epithelial cells. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by array
Platform:
GPL9542
2 Samples
Download data: GPR
Series
Accession:
GSE18929
ID:
200018929
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