Expression of Hepatic Drug-Metabolizing Cytochrome P450 Enzymes and Their Intercorrelations: A Meta-Analysis
Abstract
Cytochrome P450 is a family of enzymes that catalyze reactions involved in the metabolism of drugs and other xenobiotics. These enzymes are therefore important in pharmacologic and toxicologic studies, and information on their abundances is of value in the process of scaling in vitro data to in vivo metabolic parameters. A meta-analysis was applied to data on the abundance of human hepatic cytochrome P450 enzymes in Caucasian adult livers (50 studies). Despite variations in the methods used to measure the abundance of enzymes, agreement between the studies in 26 different laboratories was generally good. Nonetheless, some heterogeneity was detected (Higgins and Thompson heterogeneity test). More importantly, large interindividual variability was observed in the collated data. Positive correlations between the expression levels of some cytochrome P450 enzymes were found in the abundance data, including the following pairs: CYP3A4/CYP3A5*1/*3 (Rs = 0.70, P < 0.0001, n = 52), CYP3A4/CYP2C8 (Rs = 0.68, P < 0.0001, n = 134), CYP3A4/CYP2C9 (Rs = 0.55, P < 0.0001, n = 71), and CYP2C8/CYP2C9 (Rs = 0.55, P < 0.0001, n = 99). These correlations can be used to demonstrate common genetic transcriptional mechanisms.
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Several studies have reported substantial differences in CYP expression and significant differences in the activity of different CYP isoforms in HLM.
“Several studies have reported the substantial differences in CYP expression and significant differences in the activity of different CYP isoforms in HLM [68,75,76].”
From Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling (2019) · cites this paper as [75]
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References 80 · Cited by 212
- Authors
- Achour, B., Barber, J., & Rostami-Hodjegan, A.
- Affiliations
- University of Manchester (GB)
- Venue
- Drug Metabolism and Disposition
- Publisher
- Elsevier BV
- Published
- 2014-08
- Volume
- 42
- Issue
- 8
- Pages
- 1349-1356
- ISSN
- 0090-9556 (ISSN-L)
- OpenAlex
- W2109634874
- Cited by
- 212
- References
- 80
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 15 · 2023: 16 · 2022: 28 · 2021: 30 · 2020: 27 · 2019: 32 · 2018: 9 · 2017: 17 · 2016: 11 · 2015: 11 · 2014: 2
- FWCI
- 2.43
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Drug Metabolism and Disposition (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (submittedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
- Keywords
- cytochrome P450, hepatic drug metabolism, CYP3A4, CYP3A5, CYP2C8, CYP2C9, enzyme expression, interindividual variability, human liver
- MeSH terms
- Cytochrome P-450 Enzyme System, Female, Humans, Individuality, Liver, Male, Microsomes, Liver, Gene Expression
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