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pmid:28831409
The idiosyncratic drug-induced gene expression changes in HepG2 cells.
J Jiang · K Mathijs · L Timmermans · S M Claessen · A Hecka · J Weusten · R Peters · J H van Delft · J C S Kleinjans · D G J Jennen · T M de Kok
Data in brief · 2017 doi:10.1016/j.dib.2017.07.074
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Experiment
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Data
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Analysis
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Complete file
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However, the molecular mechanisms of this inflammation-associated idiosyncratic drug hepatotoxicity remain unknown. We exposed HepG2 cells with high and low doses of three idiosyncratic (I) and three non-idiosyncratic (N) compounds, in the presence (I+ and N+) or absence (I- and N-) of a cytokine mix for 6, 12 and 24 h. To investigate the genome-wide expression patterns, microarray was performed using the Agilent 4×44K Whole Human Genome chips. The data presented in this DIB include the expression of genes participating in the ceramide metabolism, ER stress, apoptosis and cell survival pathways. The functions of these genes were illustrated in our associated article (Jiang et al., 2017) [1]. 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