CYP1A2 mRNA Expression Rather than Genetic Variants Indicate Hepatic CYP1A2 Activity

CYP1A2, one of the most abundant hepatic cytochrome P450 enzymes, is involved in metabolism of several drugs and carcinogenic compounds. Data on the significance of <i>CYP1A2</i> genetic polymorphisms in enzyme activity are highly inconsistent; therefore, the impact of <i>CYP1A2<...

Full description

Saved in:
Bibliographic Details
Main Authors: Ferenc Fekete (Author), Katalin Mangó (Author), Annamária Minus (Author), Katalin Tóth (Author), Katalin Monostory (Author)
Format: Book
Published: MDPI AG, 2022-02-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:CYP1A2, one of the most abundant hepatic cytochrome P450 enzymes, is involved in metabolism of several drugs and carcinogenic compounds. Data on the significance of <i>CYP1A2</i> genetic polymorphisms in enzyme activity are highly inconsistent; therefore, the impact of <i>CYP1A2</i> genetic variants (−3860G>A, −2467delT, −739T>G, −163C>A, 2159G>A) on mRNA expression and phenacetin <i>O</i>-dealkylation selective for CYP1A2 was investigated in human liver tissues and in psychiatric patients belonging to Caucasian populations. <i>CYP1A2*1F</i>, considered to be associated with high CYP1A2 inducibility, is generally identified by the presence of −163C>A polymorphism; however, we demonstrated that −163C>A existed in several haplotypes (<i>CYP1A2*1F</i>, <i>CYP1A2*1L</i>, <i>CYP1A2*1M</i>, <i>CYP1A2*1V</i>, <i>CYP1A2*1W</i>), and consequently, <i>CYP1A2*1F</i> was a much rarer allelic variant (0.4%) than reported in Caucasian populations. Of note, −163C>A polymorphism was found to result in an increase of neither mRNA nor the activity of CYP1A2. Moreover, hepatic CYP1A2 activity was associated with hepatic or leukocyte mRNA expression rather than genetic polymorphisms of <i>CYP1A2</i>. Consideration of non-genetic phenoconverting factors (co-medication with CYP1A2-specific inhibitors/inducers, tobacco smoking and non-specific factors, including amoxicillin+clavulanic acid therapy or chronic alcohol consumption) did not much improve genotype-phenotype estimation. In conclusion, <i>CYP1A2</i>-genotyping is inappropriate for the prediction of CYP1A2 function; however, CYP1A2 mRNA expression in leukocytes can inform about patients' CYP1A2-metabolizing capacity.
Item Description:10.3390/pharmaceutics14030532
1999-4923