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Links from GEO DataSets

Items: 20

1.

Gene expression data from precision cut human liver slices treated to diclofenac

(Submitter supplied) Drug-induced liver injury (DILI) is an important clinical problem. Here we used a genomics approach to establish the critical drug-induced toxicity pathways that act in synergy with the pro-inflammatory cytokine tumor necrosis factor (TNF) to cause cell death of liver HepG2 cells. Transcriptomics of the cell injury stress response pathways initiated by two hepatoxicants, diclofenac and carbamazepine, revealed the endoplasmic reticulum (ER) stress/translational initiation signaling and Nrf2 antioxidant signaling as two major affected pathways, which was similar to that observed for the majority of ~80 DILI compounds in primary human hepatocytes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
10 Samples
Download data: CEL
Series
Accession:
GSE54255
ID:
200054255
2.

Drug-induced liver injury

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL14996 GPL13158
116 Samples
Download data: CEL
Series
Accession:
GSE54257
ID:
200054257
3.

Expression data from primary mouse hepatocytes treated with Diclofenac

(Submitter supplied) Drug-induced liver injury (DILI) is an important clinical problem. Here we used a genomics approach to establish the critical drug-induced toxicity pathways that act in synergy with the pro-inflammatory cytokine tumor necrosis factor  (TNF) to cause cell death of liver HepG2 cells. Transcriptomics of the cell injury stress response pathways initiated by two hepatoxicants, diclofenac and carbamazepine, revealed the endoplasmic reticulum (ER) stress/translational initiation signaling and Nrf2 antioxidant signaling as two major affected pathways, which was similar to that observed for the majority of ~80 DILI compounds in primary human hepatocytes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL14996
10 Samples
Download data: CEL
Series
Accession:
GSE54256
ID:
200054256
4.

Expression data from human hepatocellular carcinoma cell line HepG2

(Submitter supplied) Drug-induced liver injury (DILI) is an important clinical problem. Here we used a genomics approach to establish the critical drug-induced toxicity pathways that act in synergy with the pro-inflammatory cytokine tumor necrosis factor (TNF) to cause cell death of liver HepG2 cells. Transcriptomics of the cell injury stress response pathways initiated by two hepatoxicants, diclofenac and carbamazepine, revealed the endoplasmic reticulum (ER) stress/translational initiation signaling and Nrf2 antioxidant signaling as two major affected pathways, which was similar to that observed for the majority of ~80 DILI compounds in primary human hepatocytes. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
96 Samples
Download data: CEL
Series
Accession:
GSE54254
ID:
200054254
5.

Omics-based identification of the combined effects of idiosyncratic drugs and inflammatory cytokines on the development of drug-induced liver injury

(Submitter supplied) To unravel the underlying mechanisms of inflammation-related idiosyncratic drug toxicity
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6480
252 Samples
Download data: TXT
Series
Accession:
GSE102006
ID:
200102006
6.

Expression Profiles of Primary Mouse Hepatocytes treated with Cyclosporin A and solvent control

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array; Expression profiling by array
Platforms:
GPL15967 GPL17912
46 Samples
Download data: CEL, TXT
Series
Accession:
GSE55883
ID:
200055883
7.

Expression Profiles of Primary Mouse Hepatocytes treated with Cyclosporin A and solvent control [RNA]

(Submitter supplied) The transcriptomics changes induced in Primary Mouse Hepatocytes by Cyclosporin A after treatment for 24h and 48h
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL15967
24 Samples
Download data: CEL, TXT
Series
Accession:
GSE55881
ID:
200055881
8.

Expression Profiles of Primary Mouse Hepatocytes treated with Cyclosporin A and solvent control [miRNA]

(Submitter supplied) The microRNA changes induced in Primary Mouse Hepatocytes of C57Bl6-mice by Cyclosporin A after treatment for 24h and 48h
Organism:
Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL17912
22 Samples
Download data: TXT
Series
Accession:
GSE55880
ID:
200055880
9.

RNA sequencing of MDA-MB231 and U2OS cancer cell lines exposed to the alkylating agent methyl methanesufonate (MMS) and classical chemotherapeutics 

(Submitter supplied) Understanding the mechanisms by which cells respond to chemotherapeutics is key to identifying means to improve therapy effiicacy while reducing systemic toxicity of these widely used classes of drugs. While determining the role of NRF2-GSH and ER stress in cells exposed to alkylating compounds such as methyl-methanesulfonate (MMS), we asked if these pathways could also be a general cell damage response relevant to other clinically used chemotherapeutics or if it is an alkylation specific response. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
11 Samples
Download data: TXT
10.

The genomic responses of mouse liver to diclofenac treatment reveals an immune mediated mechanism of liver injury

(Submitter supplied) Diclofenac (DCL) is a non-steroidal anti-inflammatory drug. Its use can be associated with serious adverse drug reactions most notable myocardial infarction and drug-induced liver injury (DILI). The molecular causes leading to DILI remains unclear and it seems to be multifactorial. The aims of this study is to identify the molecular mechanisms involving immune mediated inflammatory reactions and its link to DILI through whole genome gene expression profiling. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
22 Samples
Download data: CEL, CHP
Series
Accession:
GSE75277
ID:
200075277
11.

Treatment of human hepatoma and primary human hepatocyte cultures (PHH) with fatty acids and/or fatty acids and TNFa

(Submitter supplied) Treatment of the human hepatoma cell lines HepG2, HUH7 and PHH with a mixture of fatty acids caused heaptic steatosis. The combined lipid and TNFa treatment mimics inflammation. Cells were harvested and processed for microarray analysis
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13158
33 Samples
Download data: CEL, CHP
Series
Accession:
GSE122660
ID:
200122660
12.

Gene expression data from Collaborative Cross mice treated with TAK-857

(Submitter supplied) Eight (8) male mice (4 matched pairs) from each of 45 Collaborative Cross lines were treated with a single oral (gavage) dose of either vehicle (methylcellulose) or TAK-875 (600 mg/kg) to facilitate the evaluation of very early liver events in the pathogenesis of IDILI and the identification of genetic risk factors that influence toxicity susceptibility at the hepatocyte level Microarray profiling in the liver identified treatment-induced changes differing by strain and correlating with serum liver chemistries that were enriched in mitochondrial dysfunction, oxidative stress, bile acid homeostasis and immune response pathways suggesting multiple mechanisms contribute to TAK-875 toxicity. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL11180
342 Samples
Download data: CEL
Series
Accession:
GSE152852
ID:
200152852
13.

Transcriptomic analysis of endoplasmic reticulum stress (ERS) regulated genes in mouse gastrocnemius muscle

(Submitter supplied) One gastrocnemius muscle was injected with the ERS-drug tunicamycin, the other with control saline solution and muscles were used to prepare RNA.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
18 Samples
Download data: CEL
Series
Accession:
GSE123082
ID:
200123082
14.

ChIP-seq analysis of changes in H3K27ac by endoplasmic reticulum stress (ERS) in mouse primary hepatocytes.

(Submitter supplied) Mouse primary hepatocytes (MPH) prepared from C57Bl6 male adult mice were treated with the ERS-drug thapsigargin and ChIP-seq was performed using an H3K27ac antibody (Active Motif ref 39685).
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21103
8 Samples
Download data: BED
Series
Accession:
GSE122613
ID:
200122613
15.

Transcriptomic and epigenomic analysis of endoplasmic reticulum stress signaling in mouse primary hepatocytes and liver

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21103 GPL16570
52 Samples
Download data: CEL
Series
Accession:
GSE122508
ID:
200122508
16.

Transcriptomic analysis of endoplasmic reticulum stress (ERS) regulated genes in mouse primary hepatocytes.

(Submitter supplied) Mouse primary hepatocytes (MPH) prepared from C57Bl6 male adult mice were treated with the ERS-drug thapsigargin and used to prepare RNA.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
6 Samples
Download data: CEL
Series
Accession:
GSE122507
ID:
200122507
17.

Transcriptomic analysis of endoplasmic reticulum stress (ERS) regulated genes in the liver of NFIL3 KO mice.

(Submitter supplied) Livers from wild-type (WT) or NFIL3 knock-out (NFIL3 KO) C57Bl6 mal adult mice treated with the ERS-drug tunicamycin were used to prepare RNA.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
20 Samples
Download data: CEL
Series
Accession:
GSE122506
ID:
200122506
18.

Comparative hepatic transcriptome analyses revealed possible pathogenic mechanisms of fasiglifam (TAK-875)-induced acute liver injury in mice

(Submitter supplied) Fasiglifam (TAK-875), a G protein-coupled receptor 40 (GPR40) agonist, was a drug candidate for type 2 diabetes. However, its development was terminated in phase 3 trials due to liver safety concerns. Although TAK-875 was reported to inhibit hepatobiliary transporters and disturb bile acid disposition, pathogenic mechanisms of TAK-875-induced liver injury are not fully understood. In this study, we sought to identify the mechanisms with a hepatic genome-wide transcriptomic analysis in a murine model. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
4 Samples
Download data: TXT
Series
Accession:
GSE112140
ID:
200112140
19.

Expression Profiles of mRNAs and microRNAs in HepG2 cells treated with Cyclosporin A and solvent control

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus; Rattus norvegicus
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platforms:
GPL16311 GPL16968
72 Samples
Download data: CEL, TXT
Series
Accession:
GSE45802
ID:
200045802
20.

Expression Profiles of microRNAs of HepG2 cells treated with Cyclosporin A and solvent control

(Submitter supplied) The microRNA changes induced in the human liver cell line HepG2 by Cyclosporin A after treatment for 12h, 24h, 48h and 72h
Organism:
Homo sapiens; Rattus norvegicus; Mus musculus
Type:
Non-coding RNA profiling by array
Platform:
GPL16968
36 Samples
Download data: TXT
Series
Accession:
GSE45800
ID:
200045800
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