Literature DB >> 15228164

Genetics of the variable expression of CYP3A in humans.

Leszek Wojnowski1.   

Abstract

CYP3A isozymes participate in the metabolism of 45-60% of currently used drugs and of a variety of other compounds such as steroid hormones, toxins, and carcinogens. The CYP3A expression status is a major determinant of drug efficacy and safety, and it may also affect an individual's predisposition to certain cancers. The inter- and intraindividual expression of CYP3A is variable because of a complex interplay between genetic and environmental factors. Markers predictive of the individual CYP3A activity could improve therapies with CYP3A substrates by personalised dose adjustments, but their development has been slower than for other drug-metabolizing enzymes. Here we summarize the recent progress in genomics and regulation of CYP3A. The recently described markers of the CYP3A5 and CYP3A7 polymorphisms should facilitate the development of isozyme-specific activity markers for the individual CYP3A isozymes, including CYP3A4.

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Year:  2004        PMID: 15228164     DOI: 10.1097/00007691-200404000-00019

Source DB:  PubMed          Journal:  Ther Drug Monit        ISSN: 0163-4356            Impact factor:   3.681


  28 in total

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5.  Explaining variability in ciclosporin exposure in adult kidney transplant recipients.

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7.  Drug monitoring of imatinib levels in patients undergoing therapy for chronic myeloid leukaemia: comparing plasma levels of responders and non-responders.

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Review 8.  Effect of cytokine and pharmacogenomic genetic polymorphisms in transplantation.

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Review 9.  CYP3A5 polymorphism, amlodipine and hypertension.

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10.  Molecular population genetics of human CYP3A locus: signatures of positive selection and implications for evolutionary environmental medicine.

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Journal:  Environ Health Perspect       Date:  2009-06-18       Impact factor: 9.031

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