4.2 Review

Polymorphisms in cytochrome P450 oxidoreductase and its effect on drug metabolism and efficacy

Journal

PHARMACOGENETICS AND GENOMICS
Volume 27, Issue 9, Pages 337-346

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/FPC.0000000000000297

Keywords

cytochrome P450 oxidoreductase; cytochrome P450; drug metabolism; drug therapy; genetic polymorphisms

Funding

  1. China Scholarship Council
  2. National Natural Science Foundation of China [30901834]
  3. Hunan Provincial Natural Science Foundation of China [12K005]
  4. China Postdoctoral Science Foundation [2016M602434]
  5. [NCET-11-0509]

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Cytochrome P450 oxidoreductase (POR) has played a potential role in the metabolism of drugs and steroids by supplying electrons to microsomal cytochrome P450 (CYP) enzymes. More than 200 different POR mutations and polymorphisms causing more than 130 amino acid changes in the POR protein have been reported since 2004. A503V is a common amino acid sequence variant encoded by POR*28, whereas A287P and R457H are the most common disease-causing mutations in Europeans and Asians, respectively. Polymorphisms in the POR gene can affect POR activity, CYP-mediated drug metabolism activities, and the efficacy of several clinically used drugs. The effects of POR variants on CYP activities are substrate dependent. In this review, recent research on the effects of POR genetic polymorphisms on drug metabolism and therapy has been summarized and discussed, which can contribute to the rational use of drugs in clinic and the development of personalized medicine. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.

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