Pharmacogenetics of aldo-keto reductase 1C (AKR1C) enzymes

被引:7
作者
Alshogran, Osama Y. [1 ]
机构
[1] Jordan Univ Sci & Technol, Fac Pharm, Dept Clin Pharm, Irbid 22110, Jordan
关键词
Metabolism; aldo-keto reductase 1C; pharmacogenetics; single nucleotide polymorphism; disease susceptibility; treatment outcome; POLYCYSTIC-OVARY-SYNDROME; SINGLE-NUCLEOTIDE POLYMORPHISMS; IN-VITRO METABOLISM; NON-HODGKIN-LYMPHOMA; 20-ALPHA-HYDROXYSTEROID DEHYDROGENASE AKR1C1; MENOPAUSAL HORMONE-THERAPY; CARBONYL REDUCING ENZYMES; PROSTAGLANDIN-F SYNTHASE; HUMAN LIVER CYTOSOL; PROSTATE-CANCER;
D O I
10.1080/17425255.2017.1376648
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Genetic variation in metabolizing enzymes contributes to variable drug response and disease risk. Aldo-keto reductase type 1C (AKR1C) comprises a sub-family of reductase enzymes that play critical roles in the biotransformation of various drug substrates and endogenous compounds such as steroids. Several single nucleotide polymorphisms have been reported among AKR1C encoding genes, which may affect the functional expression of the enzymes.Areas covered: This review highlights and comprehensively discusses previous pharmacogenetic reports that have examined genetic variations in AKR1C and their association with disease development, drug disposition, and therapeutic outcomes. The article also provides information about the effect of AKR1C genetic variants on enzyme function in vitro.Expert opinion: The current evidence that links the effect of AKR1C gene polymorphisms to disease progression and development is inconsistent and needs further validation, despite of the tremendous knowledge available. Information about association of AKR1C genetic variants and drug efficacy, safety, and pharmacokinetics is limited, thus, future studies that advance our understanding about these relationships and their clinical relevance are needed. It is imperative to achieve consistent findings before the potential translation and adoption of AKR1C genetic variants in clinical practice.
引用
收藏
页码:1063 / 1073
页数:11
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