High-throughput and combinatorial gene expression on a chip for metabolism-induced toxicology screening.

Nat Commun

1] Solidus Biosciences Inc., 409 Illinois Street, Suite 2073, San Francisco, California 94158, USA [2] Department of Chemical and Biomedical Engineering, Cleveland State University, Cleveland, Ohio 44115, USA.

Published: May 2014

Differential expression of various drug-metabolizing enzymes (DMEs) in the human liver may cause deviations of pharmacokinetic profiles, resulting in interindividual variability of drug toxicity and/or efficacy. Here, we present the 'Transfected Enzyme and Metabolism Chip' (TeamChip), which predicts potential metabolism-induced drug or drug-candidate toxicity. The TeamChip is prepared by delivering genes into miniaturized three-dimensional cellular microarrays on a micropillar chip using recombinant adenoviruses in a complementary microwell chip. The device enables users to manipulate the expression of individual and multiple human metabolizing-enzyme genes (such as CYP3A4, CYP2D6, CYP2C9, CYP1A2, CYP2E1 and UGT1A4) in THLE-2 cell microarrays. To identify specific enzymes involved in drug detoxification, we created 84 combinations of metabolic-gene expressions in a combinatorial fashion on a single microarray. Thus, the TeamChip platform can provide critical information necessary for evaluating metabolism-induced toxicity in a high-throughput manner.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132844PMC
http://dx.doi.org/10.1038/ncomms4739DOI Listing

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