Skip to main navigation Skip to search Skip to main content

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

  • Seok Joon Kwon
  • , Dong Woo Lee
  • , Dhiral A. Shah
  • , Bosung Ku
  • , Sang Youl Jeon
  • , Kusum Solanki
  • , Jessica D. Ryan
  • , Douglas S. Clark
  • , Jonathan S. Dordick
  • , Dong Woo Lee
  • School of Engineering
  • Samsung Electro-Mechanics
  • Solidus Biosciences Inc.
  • Cleveland State University
  • University of California Press

Research output: Contribution to journalArticlepeer-review

85 Scopus citations

Abstract

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. © 2014 Macmillan Publishers Limited. All rights reserved.
Original languageEnglish
Article number3739
JournalNature Communications
Volume5
DOIs
StatePublished - May 6 2014

Cite this