Cytochrome P450 and xenobiotic receptor humanized mice

Frank J. Gonzalez, Aiming Yu

Research output: Contribution to journalArticle

122 Scopus citations

Abstract

Most xenobiotics that enter the body are subjected to metabolism that functions primarily to facilitate their elimination. Metabolism of certain xenobiotics can also result in the production of electrophilic derivatives that can cause cell toxicity and transformation. Many xenobiotics can also activate receptors that in turn induce the expression of genes encoding xenobiotic-metabolizing enzymes and xenobiotic transporters. However, there are marked species differences in the way mammals respond to xenobiotics, which are due in large part to molecular differences in receptors and xenobiotic- metabolizing enzymes. This presents a problem in extrapolating data obtained with rodent model systems to humans. There are also polymorphisms in xenobiotic-metabolizing enzymes that can impact drug therapy and cancer susceptibility. In an effort to generate more reliable in vivo systems to study and predict human response to xenobiotics, humanized mice are under development.

Original languageEnglish (US)
Pages (from-to)41-64
Number of pages24
JournalAnnual Review of Pharmacology and Toxicology
Volume46
DOIs
StatePublished - 2006
Externally publishedYes

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Keywords

  • Cancer
  • CYP
  • Drug metabolism
  • Gene activation
  • Ligands
  • Nuclear receptor
  • Pharmacogenetics
  • Pharmacokinetics
  • Toxicity
  • Transgenic mouse model

ASJC Scopus subject areas

  • Pharmacology
  • Toxicology

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