MicroRNA regulation of the major drug-metabolizing enzymes and related transcription factors

Drug Metab Rev. 2015 Aug;47(3):320-34. doi: 10.3109/03602532.2015.1076438. Epub 2015 Aug 20.

Abstract

Identifying novel mechanisms contributing to patient variability of drug response is a major goal of personalized medicine. Epigenetic regulation of gene expression by microRNA (miRNA) impacts a broad range of cellular processes, but knowledge of its regulation of drug-metabolizing enzymes (DMEs) is more limited. This review provides an introduction to miRNA and their functionality and summarizes known miRNA regulation of DME families, including the cytochrome P450s, UDP-glucuronoslytransferases, glutathione-S-transferases, sulfotransferases and aldo-keto reductases, and the transcription factors known to be involved in DME regulation.

Keywords: epigenetic regulation; metabolizing enzymes; miRNA; phase I metabolism; phase II metabolism; transcription factors.

Publication types

  • Review

MeSH terms

  • Aldo-Keto Reductases / genetics
  • Aldo-Keto Reductases / metabolism
  • Animals
  • Biotransformation / genetics*
  • Cytochrome P-450 Enzyme System / genetics
  • Cytochrome P-450 Enzyme System / metabolism
  • Epigenesis, Genetic
  • Gene Expression Regulation, Enzymologic*
  • Glucuronosyltransferase / genetics
  • Glucuronosyltransferase / metabolism
  • Glutathione Transferase / genetics
  • Glutathione Transferase / metabolism
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Sulfotransferases / genetics
  • Sulfotransferases / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism

Substances

  • MicroRNAs
  • Transcription Factors
  • Cytochrome P-450 Enzyme System
  • Aldo-Keto Reductases
  • Glucuronosyltransferase
  • Glutathione Transferase
  • Sulfotransferases