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Links from GEO DataSets

Items: 20

1.

Genome-wide methylation analysis of AOM/DSS-induced colon tumors

(Submitter supplied) Genome-wide methylation analysis was performed by methylated DNA immunoprecipitation (MeDIP)-CpG island (CGI) microarray analysis to identify candidate CGIs specifically methylated in mouse colon tumors associated with colitis. We sucessfully identified 23 candidate CGIs methylated in tumors.
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array
Platform:
GPL10324
2 Samples
Download data: TXT
Series
Accession:
GSE21333
ID:
200021333
2.

H3K27me3 analysis in mouse colonic epithelial cells

(Submitter supplied) H3K27me3 statuses were analyzed in normal mouse colonic epithelial cells and in those exposed to DSS-induced colitis, and aberrant changes of H3K27me3 by DSS-induced colitis were identified.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10324
3 Samples
Download data: TXT
Series
Accession:
GSE74007
ID:
200074007
3.

Identification of microRNA landscape of inflammation-induced colorectal carcinogenesis

(Submitter supplied) Inflammatory conditions can contribute to tumor formation. However, any clear marker predicting progression to cancer are still lacking. The aim of our study was to analyze microRNA modulations accompanying inflammation-induced tumor development to determine whether these microRNA may jointly affect the expression of genes involved in cancer. For this purpose, we used the well-established azoxymethane (AOM)/dextran sulfate sodium (DSS)-induced mouse model of colitis-associated cancer. more...
Organism:
Homo sapiens; Rattus norvegicus; synthetic construct; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL15644
50 Samples
Download data: TXT
Series
Accession:
GSE38443
ID:
200038443
4.

Transcriptome and Methylome Changes During the Progression of Colitis-accelerated Colon Cancer in Mouse and the Blockage by Curcumin

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL19057
18 Samples
Download data: TXT
Series
Accession:
GSE102648
ID:
200102648
5.

Methylome Changes During the Progression of Colitis-accelerated Colon Cancer in Mouse and the Blockage by Curcumin

(Submitter supplied) Inflammation is highly associated with colon carcinogenesis. Epigenetic mechanisms play an important role in the initiation and progression of colon cancer. Curcumin is a dietary cancer preventive phytochemical with promising effect in suppressing colitis-associated colon cancer (CAC) in azoxymethane (AOM) and dextran sulfate sodium (DSS) mouse model. In the present study, we confirmed the effect of curcumin in suppressing colon cancer. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL19057
6 Samples
Download data: TXT
Series
Accession:
GSE102645
ID:
200102645
6.

Transcriptome Changes During the Progression of Colitis-accelerated Colon Cancer in Mouse and the Blockage by Curcumin

(Submitter supplied) Inflammation is highly associated with colon carcinogenesis. Epigenetic mechanisms play an important role in the initiation and progression of colon cancer. Curcumin is a dietary cancer preventive phytochemical with promising effect in suppressing colitis-associated colon cancer (CAC) in azoxymethane (AOM) and dextran sulfate sodium (DSS) mouse model. In the present study, we confirmed the effect of curcumin in suppressing colon cancer. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19057
12 Samples
Download data: TXT
Series
Accession:
GSE102342
ID:
200102342
7.

Altered epigenetic programming links intestinal inflammation to colon cancer

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL13112
19 Samples
Download data: BW
Series
Accession:
GSE57569
ID:
200057569
8.

Altered epigenetic programming links intestinal inflammation to colon cancer (RNA-seq)

(Submitter supplied) This study uses whole-transcriptome sequencing to characterize the transcriptomes of the AOM/DSS mouse model. In this model, mice are treated with dextran sodium sulfate (DSS) to induce colitis. When this treatment is preceded by injections of the weak carcinogen azoxymethane (AOM) the mice develop intestinal tumors. Our results identify sets of differentially expressed genes which are correlated with methylation changes of the corresponding genes.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
10 Samples
Download data: TXT
Series
Accession:
GSE57533
ID:
200057533
9.

Altered epigenetic programming links intestinal inflammation to colon cancer (Bisulfite-seq)

(Submitter supplied) This study uses whole-genome bisulfite sequencing to characterize the methylomes of the AOM/DSS mouse model at single-base resolution. In this model, mice are treated with dextran sodium sulfate (DSS) to induce colitis. When this treatment is preceded by injections of the weak carcinogen azoxymethane (AOM) the mice develop intestinal tumors. Our results identify hypermethylated DMVs as a prominent feature of the colitis methylome that is conserved in intestinal adenocarcinomas. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
9 Samples
Download data: BW
Series
Accession:
GSE57527
ID:
200057527
10.

Comparison of murine colonic mucosal gene expression between postanatal day 90 (P90) to postnatal day 30 (P30)

(Submitter supplied) Comparison of murine colonic mucosal gene expression between postanatal day 90 (P90) to postnatal day 30 (P30) by whole genomic expression microarray. Gene expression profiling of colonic mucosal DNA between P90 and P30 mice. Agilent Technologies two-color labelling kit and genomic hybridization protocol was utilized.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
4 Samples
Download data: TXT
Series
Accession:
GSE19506
ID:
200019506
11.

Comparison of murine colonic mucosal DNA from postnatal day 90 (P90) to postnatal day 30 (P30) by MSAM

(Submitter supplied) DNA methylation profiling of colonic mucosal DNA between P90 and P30 mice. 0.5ug of DNA was serially digested with SmaI and XmaI followed by an adaptor ligation and adaptor mediated PCR amplification
Organism:
Mus musculus
Type:
Methylation profiling by genome tiling array
Platform:
GPL9158
2 Samples
Download data: TXT
Series
Accession:
GSE18031
ID:
200018031
12.

DNA methylation patterns separate senescence from malignant transformation potential in human cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Methylation profiling by array
Platforms:
GPL10332 GPL13534
39 Samples
Download data: IDAT, TXT
Series
Accession:
GSE91071
ID:
200091071
13.

DNA methylation patterns separate senescence from malignant transformation potential in human cells [gene expression]

(Submitter supplied) Replicative senescent cells reportedly share similar DNA methylation changes with cancer cells, which are purported to facilitate tumorigenesis in cells bypassing senescence. However, we now report biologically critical and distinct patterns of DNA methylation evolution between replicative and oncogene-induced senescence and transformation in a classic human cell transformation model. While overall DNA methylation losses and gains occur in both replicative senescent and transformed cells, the patterns evolve more programmatically for the former and stochastically for the latter. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10332
8 Samples
Download data: TXT
Series
Accession:
GSE91070
ID:
200091070
14.

DNA methylation patterns separate senescence from malignant transformation potential in human cells [methylation]

(Submitter supplied) Replicative senescent cells reportedly share similar DNA methylation changes with cancer cells, which are purported to facilitate tumorigenesis in cells bypassing senescence. However, we now report biologically critical and distinct patterns of DNA methylation evolution between replicative and oncogene-induced senescence and transformation in a classic human cell transformation model. While overall DNA methylation losses and gains occur in both replicative senescent and transformed cells, the patterns evolve more programmatically for the former and stochastically for the latter. more...
Organism:
Homo sapiens
Type:
Methylation profiling by array
Platform:
GPL13534
31 Samples
Download data: IDAT, TXT
Series
Accession:
GSE91069
ID:
200091069
15.

In vivo loss of TET2 and TET2 results in aberrant differentiation and homeostasis in the small intestine

(Submitter supplied) Although much research has been done on the diversity of the gut microbiome, little is known about how it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested to operate at the interface between the microbiota and the intestinal epithelium. We performed whole-genome bisulfite sequencing on conventionally raised and germ-free mice, and discovered that exposure to commensal microbiota induced localized DNA methylation changes at regulatory elements, which are TET2/3-dependent. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL21273
6 Samples
Download data: BEDGRAPH
Series
Accession:
GSE206169
ID:
200206169
16.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation [ATAC-Seq]

(Submitter supplied) Although much research has been done on the diversity of gut microbiome, little is known about the way it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested as operating at the interface between the microbiota and the intestinal epithelium cells (IECs). Using genome-wide analyses, we discovered that exposure to microbiota induced both global DNA hypomethylation and localized changes at regulatory elements, which culminates in activation of a set of “early sentinel” response genes that play a role in maintaining gut homeostasis. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: TXT
Series
Accession:
GSE141458
ID:
200141458
17.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL21273 GPL13112
32 Samples
Download data: BEDGRAPH, TXT
Series
Accession:
GSE137037
ID:
200137037
18.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation [RNA-seq]

(Submitter supplied) Although much research has been done on the diversity of gut microbiome, little is known about the way it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested as operating at the interface between the microbiota and the intestinal epithelium cells (IECs). Using genome-wide analyses, we discovered that exposure to microbiota induced both global DNA hypomethylation and localized changes at regulatory elements, which culminates in activation of a set of “early sentinel” response genes that play a role in maintaining gut homeostasis. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
12 Samples
Download data: TXT
Series
Accession:
GSE136840
ID:
200136840
19.

The intestinal microbiota programs DNA methylation to control tissue homeostasis and inflammation [BiSulfite-seq]

(Submitter supplied) Although much research has been done on the diversity of gut microbiome, little is known about the way it influences intestinal homeostasis under normal and pathogenic conditions. Epigenetic mechanisms have recently been suggested as operating at the interface between the microbiota and the intestinal epithelium cells (IECs). Using genome-wide analyses, we discovered that exposure to microbiota induced both global DNA hypomethylation and localized changes at regulatory elements, which culminates in activation of a set of “early sentinel” response genes that play a role in maintaining gut homeostasis. more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
8 Samples
Download data: BEDGRAPH
Series
Accession:
GSE125978
ID:
200125978
20.

DNA methylation statuses of 293FT cells with TET depletion and NOC18 treatment

(Submitter supplied) DNA methylation statuses of 293FT cells with TET depletion and NOC18 treatment
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL21145
32 Samples
Download data: TXT
Series
Accession:
GSE117528
ID:
200117528
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