Document Detail

Pharmacogenetics of P450 oxidoreductase: implications in drug metabolism and therapy.
MedLine Citation:
PMID:  23047293     Owner:  NLM     Status:  In-Data-Review    
The redox reaction of cytochrome P450 enzymes (CYP) is an important physiological and biochemical reaction in the human body, as it is involved in the oxidative metabolism of both endogenous and exogenous substrates. Cytochrome P450 oxidoreductase (POR) is the only obligate electron donor for all of the hepatic microsomal CYP enzymes. It plays a crucial role in drug metabolism and treatment by not only acting as an electron donor involved in drug metabolism mediated by CYP enzymes but also by directly inducing the transformation of some antitumor precursors. Studies have found that the gene encoding human POR is highly polymorphic, which is of considerable clinical significance as it affects the metabolism and curative effects of clinically used drugs. This review aims to discuss the effect of POR and its genetic polymorphisms on drug metabolism and therapy, as well as the potential mechanisms of POR pharmacogenetics.
Lei Hu; Wei Zhuo; Yi-Jing He; Hong-Hao Zhou; Lan Fan
Related Documents :
8538363 - Neurochemical correlates of antiepileptic drugs in the genetically epilepsy-prone rat (...
24755703 - Combination of mechanical atherectomy and drug-eluting balloons for femoropopliteal in-...
18465563 - 26th national medicinal chemistry symposium - developments in chemokines, carbohydrates...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Pharmacogenetics and genomics     Volume:  22     ISSN:  1744-6880     ISO Abbreviation:  Pharmacogenet. Genomics     Publication Date:  2012 Nov 
Date Detail:
Created Date:  2012-10-10     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101231005     Medline TA:  Pharmacogenet Genomics     Country:  United States    
Other Details:
Languages:  eng     Pagination:  812-9     Citation Subset:  IM    
aHunan Key laboratory of Pharmacogenetics, Pharmacogenetics Research Institute, Institute of Clinical Pharmacology, Central South University, Changsha, Hunan, People's Republic of China bInstitute for Pharmacogenomics & Individualized Therapy, University of North Carolina, Chapel Hill, North Carolina, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Analysis of treatment-resistant schizophrenia and 384 markers from candidate genes.
Next Document:  Novel far-visible and near-infrared pH probes based on styrylcyanine for imaging intracellular pH in...