U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

Cell death and regenerative proliferation pathways in hepatocellular carcinoma: The effect of furan on B6C3F1 mouse global gene expression in liver

(Submitter supplied) Furan is a mouse and rat hepatocarcinogen. We sought to determine the dose-dependent changes in gene expression upon exposure of B6C3F1 mice to furan in order to better understand furan’s mode of action. Adult female B6C3F1 mice were exposed to 1, 2, 4 or 8 mg/kg bw furan or vehicle control (corn oil) for three weeks and sacrificed four hours after the final exposure.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
23 Samples
Download data: TXT
Series
Accession:
GSE48644
ID:
200048644
2.

The effect of BrdU on gene expression profiles of B6C3F1 mice treated with furan

(Submitter supplied) Furan is a mouse and rat hepatocarcinogen. We sought to determine the dose-dependent changes in gene expression upon exposure of B6C3F1 mice to furan in order to better understand furan’s mode of action.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
14 Samples
Download data: TXT
Series
Accession:
GSE54078
ID:
200054078
3.

Toxicogenomic Assessment of Liver Responses following subchronic exposure to furan in Fischer F344 rats

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL15084 GPL14860
65 Samples
Download data: TXT
Series
Accession:
GSE62808
ID:
200062808
4.

Toxicogenomic Assessment of Liver Responses following subchronic exposure to furan in Fischer F344 rats [miRNA]

(Submitter supplied) Furan is a widely used industrial chemical and a common contaminant in heated foods. Chronic furan exposure has been shown to cause cholangiocarcinoma and hepatocellular tumors at doses of 2 mg/kg bw/day with gender differences in frequency and severity. The hepatic transcriptional alterations induced by low doses of furan (doses below those inducing liver tumors) and the potential mechanisms underlying gender differences are largely unexplored. more...
Organism:
Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL14860
16 Samples
Download data: TXT
Series
Accession:
GSE62807
ID:
200062807
5.

Toxicogenomic Assessment of Liver Responses following subchronic exposure to furan in Fischer F344 rats [cRNA]

(Submitter supplied) Furan is a widely used industrial chemical and a common contaminant in heated foods. Chronic furan exposure has been shown to cause cholangiocarcinoma and hepatocellular tumors at doses of 2 mg/kg bw/day with gender differences in frequency and severity. The hepatic transcriptional alterations induced by low doses of furan (doses below those inducing liver tumors) and the potential mechanisms underlying gender differences are largely unexplored. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL15084
49 Samples
Download data: TXT
Series
Accession:
GSE62806
ID:
200062806
6.

Acute Effects Caused by the Rodent Non-Genotoxic Carcinogen Diethylhexylphthalate

(Submitter supplied) Acute effects caused by the non-genotoxic carcinogen and peroxisome proliferator (PP) diethylhexylphthalate (DEHP) in the mouse liver
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
24 Samples
Download data: CEL
Series
Accession:
GSE55733
ID:
200055733
7.

Early MicroRNA Indicators of PPARα Pathway Activation in the Liver

(Submitter supplied) In this study, we measured liver miRNA in male B6C3F1 mice exposed to a known chemical activator of the peroxisome proliferator-activated receptor alpha (PPARα) pathway, di(2-ethylhexyl) phthalate (DEHP), for 7 and 28 days at concentrations of 0, 750, 1500, 3000, or 6000 ppm in feed. At the highest dose tested, DEHP altered 61 miRNAs after 7 days and 171 miRNAs after 28 days of exposure, with 48 overlapping miRNAs between timepoints. more...
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL19057
48 Samples
Download data: TXT
Series
Accession:
GSE144988
ID:
200144988
8.

Application of toxicogenomics for the risk assessment of the food contaminant acetamide

(Submitter supplied) Acetamide (CAS 60-35-5) is detected in common foods including milk, eggs, beef, and roasted coffee beans. Chronic rodent bioassays using high doses (≥1000 mg/kg/day) suggest acetamide is a group 2B possible human carcinogen due to the induction of liver tumors. Weight-of-evidence indicates acetamide is not genotoxic, and therefore a threshold response is expected. We used a toxicogenomics approach in Wistar rats gavaged daily for 7 and 28 days to determine the benchmark dose (BMD), and investigate its mode of action from differential gene expression. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20084
145 Samples
Download data: TXT
Series
Accession:
GSE132815
ID:
200132815
9.

Gene expression profiling to recognize specific features of (non-) genotoxic carcinogens

(Submitter supplied) The current test strategy for carcinogenicity is generally based on in vitro and in vivo genotoxicity assays. Non-genotoxic carcinogens (NGTXC) are negative for genotoxicity and go undetected. Therefore, alternative tests to detect these chemicals are urgently needed. NGTXC act through different modes of action, which complicates the development of such assays. We have demon­strated recently in primary mouse hepatocytes that some, but certainly not all, NGTXC can be categorized according to their mode of action based on feature detection at a gene expression level (Schaap et al. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL17198
88 Samples
Download data: CEL
Series
Accession:
GSE47345
ID:
200047345
10.

Gene expression profiling to recognize specific features of non-genotoxic carcinogens

(Submitter supplied) The current test strategy for carcinogenicity is generally based on in vitro and in vivo genotoxicity assays. Non-genotoxic carcinogens (NGTXC) are negative for genotoxicity and go undetected. Therefore, alternative tests to detect these chemicals are urgently needed. NGTXC act through different modes of action, which complicates the development of such assays. We have demonstrated recently in primary mouse hepatocytes that some, but certainly not all, NGTXC can be categorized according to their mode of action based on feature detection at a gene expression level (Schaap et al. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL15125
111 Samples
Download data: CEL, TXT
Series
Accession:
GSE44088
ID:
200044088
11.

MicroRNA and mRNA biomarkers for short-term in vivo genotoxic and non-genotoxic carcinogen classification

(Submitter supplied) Many innovative techniques and scientific improvements are available to tackle societal concerns, like public health safety and confining the risk of cancerous exposure to chemicals, but have not been thoroughly tested and implicated yet. We investigated if microRNA and mRNA transcription profiles can be implemented in a short-term carcinogen classifier assay. Our study is additionally focusing on the drawbacks of present-day carcinogen screening strategies and also aims to contribute to a more ethical approach towards animal use and welfare within risk assessment. more...
Organism:
Homo sapiens; Mus musculus; Rattus norvegicus
Type:
Non-coding RNA profiling by array
Platform:
GPL16560
68 Samples
Download data: TXT
Series
Accession:
GSE43847
ID:
200043847
12.

Early microRNA responses in rodent liver mediated by furan exposure establish dose thresholds for later adverse outcomes

(Submitter supplied) In this study, we evaluated the utility of microRNA (miRNA) profiling in female B6C3F1 mouse liver to indicate mechanisms of liver perturbation due to short-term exposure of the known rodent liver hepatotoxicant and carcinogen, furan. Analyses indicated a robust dose response for 34 miRNAs to furan and involvement of p53-linked pathways in furan-mediated hepatotoxicity. Overall, these results indicate mechanistic involvement of miRNA in furan carcinogenicity and provide evidence of their potential utility as accessible biomarkers of exposure and disease.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL16173
24 Samples
Download data: TXT
Series
Accession:
GSE224206
ID:
200224206
13.

Transcriptional Response of Male MutaTMMouse Spleen to Dibenzo[def,p]chrysene Exposure

(Submitter supplied) Dibenzo[def,p]chrysene (DBC) is the most carcinogenic polycyclic aromatic hydrocarbon (PAH) examined to date. We investigated the immunotoxicity of DBC, manifested as spleen atrophy following acute exposure of adult Muta™Mouse males by oral gavage. Mice were exposed to 0, 2.0, 6.2, or 20.0 mg DBC /kg-bw per day, for three days. Genotoxic endpoints (DBC-DNA adducts and lacZ mutant frequency in spleen and bone marrow, and red blood cell micronucleus frequency) and global gene expression changes were measured. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL10787
37 Samples
Download data: TXT
Series
Accession:
GSE72334
ID:
200072334
14.

MMS toxicogenomics collaboration Affymetrix data

(Submitter supplied) In order to screen candidate genes that discriminate genotoxic hepatocarcinogens from nongenotoxic ones, we compared gene expression in the liver of mice treated with 6 genotoxic hepatocarcinogens or 5 nongenotoxic hepatocarcinogens.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL339
52 Samples
Download data: CEL, CHP
Series
Accession:
GSE33248
ID:
200033248
15.

Persistence of furan-induced epigenetic aberrations in the livers of Fisher 344 rats

(Submitter supplied) Furan is a heterocyclic organic compound produced in the chemical manufacturing industry and also found in a broad range of food products, including infant formulas and baby foods. Previous reports have indicated that the adverse biological effects of furan, including its liver tumorigenicity, may be associated with epigenetic abnormalities. In the present study we investigated the persistence of epigenetic alterations in rat liver. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL14797
8 Samples
Download data: TXT
Series
Accession:
GSE63740
ID:
200063740
16.

Gene expression in C57BL/6 mice intratracheally instilled with Printex 90 carbon black nanoparticles

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
97 Samples
Download data: TXT
Series
Accession:
GSE35284
ID:
200035284
17.

Pulmonary gene expression in C57BL/6 mice intratracheally instilled with Printex 90 carbon black nanoparticles

(Submitter supplied) We investigated pulmonary mRNA profiles of female mice exposed to 0.018, 0.054 and 0.162 mg Printex 90 carbon black nanoparticles by single intra-tracheal instillation. We examined responses to these doses 1, 3 and 28 days after exposure, alongside respective controls. This study demonstrates widespread changes in inflammatory and acute phase response genes that persisted to 28 days at the highest exposure dose. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
67 Samples
Download data: TXT
Series
Accession:
GSE35193
ID:
200035193
18.

Hepatic gene expression in C57BL/6 mice intratracheally instilled with Printex 90 carbon black nanoparticles

(Submitter supplied) We investigated hepatic mRNA profiles of female mice exposed to 0.162 mg Printex 90 carbon black nanoparticles by single intra-tracheal instillation. We examined responses to this dose 1, 3 and 28 days after exposure, alongside respective controls. We show that genes part of the 3-hydroxy-3-methyl-glutaryl-CoA reductase pathway to be up-regulated by exposure to Printex 90.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4134
30 Samples
Download data: TXT
Series
Accession:
GSE35192
ID:
200035192
19.

Gene expression profiling in mouse livers after administration of both hydrogen-rich water and hydrogen gas

(Submitter supplied) Molecular hydrogen is a hopeful agent for oxidative stress-related and/or inflammatory disorders. However, the molecular mechanism for these therapeutic effects of hydrogen still remains to be fully elucidated. We examined whether molecular hydrogen alters gene expression levels in normal mouse livers by DNA microarray analysis. We identified 140 mouse genes that were upregulated (31 genes) or downregulated (109 genes) after three weeks of the inhalation of 2% hydrogen-containing air with oral intake of hydrogen-rich water. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL5642
1 Sample
Download data: GPR
Series
Accession:
GSE48826
ID:
200048826
20.

Comparative genomic analysis of Fischer F344 rat livers exposed for 90 days to 3-methylfuran or its parental compound furan.

(Submitter supplied) Transcriptomic data obtained by RNA-seq from male Fischer 344 rats treated with furan and 3-methylfuran were compared and contrasted. Microarray data from the same rats treated with furan was also used to compare microarray to RNA seq analysis.
Organism:
Rattus norvegicus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20084
172 Samples
Download data: TSV
Series
Accession:
GSE249626
ID:
200249626
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=6|qty=4|blobid=MCID_6738a658b3dde962967deb0e|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center