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Comparative Analysis of Transcriptional Responses to Genotoxic and Non-Genotoxic Agents in the Blood Cell Model TK6 and the Liver Model HepaRG

Zugehörigkeit
German Federal Institute for Risk Assessment (BfR), Department 5 - Food Safety, Unit 51 - Effect-based Analytics and Toxicogenomics, Berlin, Germany
Kreuzer, Katrin;
ORCID
0000-0002-2435-5645
Zugehörigkeit
German Federal Institute for Risk Assessment (BfR), Department 5 - Food Safety, Unit 51 - Effect-based Analytics and Toxicogenomics, Berlin, Germany
Sprenger, Heike;
ORCID
0000-0003-3810-027X
Zugehörigkeit
German Federal Institute for Risk Assessment (BfR), Department 5 - Food Safety, Unit 51 - Effect-based Analytics and Toxicogenomics, Berlin, Germany
Braeuning, Albert

Transcript signatures are a promising approach to identify and classify genotoxic and non-genotoxic compounds and are of interest as biomarkers or for future regulatory application. Not much data, however, is yet available about the concordance of transcriptional responses in different cell types or tissues. Here, we analyzed transcriptomic responses to selected genotoxic food contaminants in the human p53-competent lymphoblastoid cell line TK6 using RNA sequencing. Responses to treatment with five genotoxins, as well as with four non-genotoxic liver toxicants, were compared with previously published gene expression data from the human liver cell model HepaRG. A significant overlap of the transcriptomic changes upon genotoxic stress was detectable in TK6 cells, whereas the comparison with the HepaRG model revealed considerable differences, which was confirmed by bioinformatic data mining for cellular upstream regulators or pathways. Taken together, the study presents a transcriptomic signature for genotoxin exposure in the human TK6 blood cell model. The data demonstrate that responses in different cell models have considerable variations. Detection of a transcriptomic genotoxin signature in blood cells indicates that gene expression analyses of blood samples might be a valuable approach to also estimate responses to toxic exposure in target organs such as the liver.

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