Kathrin Klein1,2* Ulrich M. Zanger1,2
- 1Dr. Margarete Fischer Bosch Institute of Clinical Pharmacology, Stuttgart, Germany
- 2University of Tübingen, Tübingen, Germany
CYP3A4 is the most important drug metabolizing enzyme in adult humans because of its prominent expression in liver and gut and because of its broad substrate specificity, which includes drugs from most therapeutic categories and many endogenous substances. Expression and function of CYP3A4 vary extensively both intra- and interindividually thus contributing to unpredictable drug response and toxicity. A multitude of environmental, genetic, and physiological factors are known to influence CYP3A4 expression and activity. Among the best predictable sources of variation are drug–drug interactions, which are either caused by pregnane X-receptor (PXR), constitutive androstane receptor (CAR) mediated gene induction, or by inhibition through coadministered drugs or other chemicals, including also plant and food ingredients. Among physiological and pathophysiological factors are hormonal status, age, and gender, the latter of which was shown to result in higher levels in females compared to males, as well as inflammatory processes that downregulate CYP3A4 transcription. Despite the influence of these non-genetic factors, the genetic influence on CYP3A4 activity was estimated in previous twin studies and using information on repeated drug administration to account for 66% up to 88% of the interindividual variation. Although many single nucleotide polymorphisms (SNPs) within the CYP3A locus have been identified, genetic association studies have so far failed to explain a major part of the phenotypic variability. The term “missing heritability” has been used to denominate the gap between expected and known genetic contribution, e.g., for complex diseases, and is also used here in analogy. In this review we summarize CYP3A4 pharmacogenetics/genomics from the early inheritance estimations up to the most recent genetic and clinical studies, including new findings about SNPs in CYP3A4 (*22) and other genes (P450 oxidoreductase (POR), peroxisome proliferator-activated receptor alpha (PPARA)) with possible contribution to CYP3A4 variable expression.
CYP3A4 Drug Substrates and Phenotyping
CYP3A4 is in the majority of individuals abundantly expressed in liver but population variability is extremely high (>100-fold). Average microsomal content has been estimated between ∼60 pmol/mg of microsomal protein (Ohtsuki et al., 2012), 110 pmol/mg (Klein et al., 2012), and ∼150 pmol/mg (Westlind-Johnsson et al., 2003). Hepatic expression of the other CYP3A enzymes CYP3A5, CYP3A7, and CYP3A43 is much lower in adult Caucasians, although CYP3A5 may contribute up to about 50% of the CYP3A pool in individuals with at least one CYP3A5*1 allele and with low CYP3A4 expression (Hustert et al., 2001a; Kuehl et al., 2001; Koch et al., 2002; King et al., 2003; Klees et al., 2005; McCune et al., 2005). The role of the minor CYP3A forms has been reviewed by others (Burk and Wojnowski, 2004; Daly, 2006). CYP3A4 is thus one of the most abundantly expressed cytochromes in human liver contributing on average about 15–30% to the microsomal P450 pool. Therefore and owing to their extraordinarily broad substrate selectivity CYP3A enzymes play a major role in the metabolism of ∼30–40% of all clinically used drugs (Evans and Relling, 1999; Zanger et al., 2008). These include preferentially lipophilic and bulky compounds from almost all therapeutic categories, including tacrolimus, cyclosporin A, erythromycin, ifosfamide, tamoxifen, benzodiazepines, several statins, antidepressants, opioids, and many more, as summarized in several previous reviews (Bu, 2006; Liu et al., 2007; Zanger et al., 2008). As CYP3A4 is also an efficient steroid hydroxylase, it has in addition an important role in the catabolism of several endogenous steroids like testosterone, progesterone, cortisol, and bile acids (Patki et al., 2003; Bodin et al., 2005).
The high sequence similarity of >85% between the CYP3A isozymes CYP3A4 and CYP3A5 leads to highly similar substrate selectivity between these isoforms (Williams et al., 2002). CYP3A4 and CYP3A5 activities are therefore not specifically discriminable although some probe drugs showed higher selectivity for CYP3A4-including, for example, erythromycin N-demethylation (Wrighton et al., 1990) and atorvastatin ortho-hydroxylation (Feidt et al., 2010). Several in vivo test substrates are available and have been compared to each other, e.g., midazolam, erythromycin, quinine, and nifedipine (Liu et al., 2007). Endogenous marker activities have also been proposed as functional CYP3A-markers, including the 6β-hydroxylation of cortisol and the 4β-hydroxylation of cholesterol, but some limitations due to considerable intraindividual variability exist (Chen et al., 2006; Fuhr et al., 2007). Remarkably, however, data obtained with different CYP3A substrates or endogenous markers are not generally well correlated to each other and have therefore to be selected carefully with respect to the expected change in activity and design of the study (Galteau and Shamsa, 2003; Chen et al., 2006; Fuhr et al., 2007). Functional CYP3A phenotyping therefore continues to be a non-trivial problem.
Degree of Heritability
CYP3A4 drug oxidation phenotypes are highly variable but unimodally distributed. Nevertheless there is indication of substantial heritability. For example, antipyrine 4-hydroxylation rate, which is mainly catalyzed by CYP3A4 (Engel et al., 1996), was reported to be largely inherited (85%) as shown in early twin studies (Penno et al., 1981). Moreover, a high degree of heritability for CYP3A4 drug oxidation capacity toward several of its substrates (erythromycin: 89% and midazolam: 96%) was estimated by a repeated drug administration approach (Ozdemir et al., 2000). A recent study used a classical twin model approach in combination with a St. John’s Wort induction regimen and quinine sulfate metabolism as CYP3A4 activity measure to elucidate genetic versus non-genetic contribution to variable CYP3A4 induction. Although the uninduced levels were not recorded, the induced CYP3A4 activity heritability was estimated to be at least 66% and environmental factors like BMI, alcohol use, and smoking habit/quantity contributed at least 20% to the variability (Rahmioglu et al., 2011).
In contrast to the genetically polymorphic CYP2D6, which is mostly determined genetically with only minor contribution by environmental factors, most of the previously studied CYP3A4 polymorphisms are either rare or lack phenotypic effect and are thus unable to explain a sizeable fraction of heritable variation. The first documented CYP3A4 polymorphism is the frequently studied proximal promoter variant CYP3A4*1B (−392A > G, rs2740574) which occurs in white populations at ∼2–9% but at higher frequencies in Africans. This single nucleotide polymorphism (SNP) was initially found to be associated with higher tumor grade and stage in prostate cancer and showed higher nifedipine oxidase activity in human livers (Rebbeck et al., 1998). Association of CYP3A4*1B with markers of advanced disease was confirmed by some but not all further studies (Keshava et al., 2004; Perera et al., 2009). Although one in vitro study on the promoter variant found higher transcriptional activity in cell culture experiments using luciferase constructs, as well as changed protein binding by electrophoretic mobility shift assay (Amirimani et al., 2003), the functional effect of this variant remains questionable given the controversial data reported in several other in vitro and human liver studies (Wandel et al., 2000; Spurdle et al., 2002; Rodríguez-Antona et al., 2005; Klein et al., 2012). Also, a study with healthy volunteers phenotyped using the dextromethorphan/methoxymorphinan ratio failed to find an association of CYP3A4*1B or *2 with CYP3A4 activity (García-Martín et al., 2002). Recently, resequencing and haplotype tagging studies have been carried out at the CYP3A locus in ethnically diverse populations (Thompson et al., 2006; Schirmer et al., 2007; Perera et al., 2009; Perera, 2010). These studies addressed the problem of “missing heritability” of CYP3A4 phenotype variability by considering haplotype structure at the CYP3A locus, which was found to be of some relevance. A markedly increased occurrence of rare variants and the presence of a homogeneous group of long-range haplotypes at high frequency were observed in non-African populations (Thompson et al., 2004). Because of their involvement in the metabolism not only of naturally occurring foreign compounds, such as flavonoids, diterpenoids, and other herbal constituents (Zhou et al., 2007) but also of endogenous chemicals such as uroporphyrin (Franklin et al., 2000) it has been suggested that molecular adaptation to the changing environment may have occurred for genes at the CYP3A locus. Thus, it has been postulated that a region from about 40 kb upstream of the CYP3A4 gene promoter to intron 6 was under positive selection in humans (Thompson et al., 2004; Chen et al., 2009). In addition, despite the controversy about the CYP3A4*1B allele, a “high haplotype homozygosity” in European Caucasians in contrast to African Americans was observed, which may indicate a negative selection pressure that eliminated the *1B allele in non-African populations (Schirmer et al., 2006). It should also be mentioned that interaction between SNP/haplotype and gender have been reported to impact on gene expression, further complicating the situation (Schirmer et al., 2007).
An intronic variant rs4646450, located in the CYP3A5 gene, has recently been associated with reduced tacrolimus dosage requirement in Japanese patients (Onizuka et al., 2011), with reduced endogenous serum dehydroepiandrosterone sulfate concentrations in over 14,000 individuals (Zhai et al., 2011) and was also associated with decreased protein expression and activity of CYP3A4 in human liver, explaining about 3–5% of hepatic variability (Klein et al., 2012). These data underline the importance of haplotype structure throughout the CYP3A locus, and they raise questions about causality of the various intronic and regulatory variants. It has been suggested generally that the most penetrant risk alleles may be of negative selective pressure and therefore be rare (Sadee, 2012). This may have led to their oversight in small sized screening studies or due to gene-environment interactions which can substantially mask genetic effects (Rahmioglu et al., 2011; Klein et al., 2012; Sadee, 2012).
Recently, however, an intron 6 variant rs35599367C > T (CYP3A4*22) was identified by a systematic screen for SNPs showing allelic mRNA expression imbalance in human liver (Wang et al., 2011). The effect of the variant was not confounded by sex or other variables and it accounted for 7% of the mRNA expression variability in a cohort of 93 liver samples. Expression in cultured cells transfected with minigenes containing exon 6, intron 6, and exon 7 reproduced the functional effect of the T-allele to decrease mRNA in vitro, suggesting that it could be the causal variant. As no associated splice variants or other hints to the exact mechanism were found, the variant was supposed to affect nascent RNA elongation rate (Wang et al., 2011; Sadee, 2012). In another recent study using 150 liver samples this variant was associated with decreased protein levels, but not when corrections were made for multiple testing (Klein et al., 2012).
Furthermore, the potential impact of CYP3A4 protein variants on drug–drug interaction was emphasized in a recent in vitro study using recombinantly expressed variant CYP3A4 proteins 3A4.2, 3A4.7, 3A4.16, and 3A4.18, where inhibitory profile differences of itraconazole and cimetidine were described in relation to the CYP3A4 variants (Akiyoshi et al., 2011). Thus, although most of the protein variants are too rare to make an impact on a population scale, individual carriers of such variants may have risk not only for impaired drug metabolism but also for a different drug–drug interaction profile.
CYP3A4 Polymorphisms – Clinical Impact
Most previous clinical studies that implemented CYP3A genotyping are not considered here because they used mainly the CYP3A5*3 polymorphism as marker. The reader is referred to other reviews on this topic (Burk and Wojnowski, 2004; Daly, 2006). Table 1 shows a selection of CYP3A4-including pharmacogenetic in vivo studies. Although the effects of the novel intron 6 variant were not very pronounced in vitro, its impact became more apparent by in vivo pharmacokinetic and pharmacodynamic studies. Significant association of CYP3A4*22 with decreased AUC0−∞ ratio in atorvastatin-treated volunteers or 1.7- to 5-fold reduced statin dose of T-allele carriers compared to non-T carriers to achieve optimal lipid control was shown in volunteer and clinical studies (Wang et al., 2011; Klein et al., 2012). The association of CYP3A4*22 with simvastatin lipid-lowering response was shown in another clinical study (Elens et al., 2011a). Furthermore, renal transplant recipients who were carriers of the low-expressor T-allele had a 33% reduced mean daily-dose requirement to reach the same tacrolimus blood concentration compared to homozygotes for the wild type allele (Elens et al., 2011b) and 1.6- to 2.0-fold higher dose-adjusted trough blood levels of tacrolimus and cyclosporine A in stable renal transplant patients (Elens et al., 2012), both indicating lower CYP3A4 activity. Despite these consistent reports, the rather low frequency of the intron 6 SNP [global minor allele frequency (MAF) 2.1%, Caucasians 3–8%] limits broader contribution to overall CYP3A4 variability.
Table 1. Selected pharmacogenetic in vivo studies with CYP3A4-relevant data.
CYP3A4 Polymorphisms – End of the Rope?
Databases are very helpful tools to get an overview on genetic variability. However, there are major collections which serve as basis for other online browsers (Table 2). The most important collection of data concerning cytochrome P450 gene haplotypes and in vitro as well as in vivo functional impact are summarized in the CYPallele homepage (updated last August 31, 2011)1. To date besides the reference CYP3A4*1 another 21 alleles are included, comprising at least 21 amino acid changes and 2 frame shift variants. Although this collection is a useful resource for functional data related to the alleles, it only provides limited information on genetic variability. Further valuable information on CYP3A4 SNPs and clinical pharmacogenetics is available on the homepage of The Pharmacogenomics Knowledgebase PharmGKB2. More comprehensive genetic information can be obtained from other databases, which collect SNP data of diverse projects, but in contrast to the CYPallele database or PharmGKB they lack cross reference to documented functional impact (Table 2). The dbSNP database3 (build 137) currently provides information on 550 SNPs for the human CYP3A4 gene of which 21% are located within the coding region, including 61 non-synonymous amino acid changes, 18 synonymous, and 4 frameshift mutations. Remarkably, for most of the coding SNPs no MAF or reliable population related distribution data is yet available. This may soon be overcome by new data releases of the international “1000 Genomes Project.” This large international collaborative project aims to generate a “Deep Catalog of Human Genetic Variation” including the entire spectrum of all types of DNA changes from SNPs and small indels (insertions/deletions) to large structural variations like copy number variants and large deletions and insertions, as well as frequency information and haplotype context (The 1000 Genomes Project Consortium, 2010)4. Next generation sequencing technologies are used to sequence the complete diploid genomes of 2500 unidentified individuals from about 25 different populations. With the release of the Integrated Phase 1 Variant set in May 2012 phased genotype calls on 1092 samples for SNPs, short indels, and large deletions from low-coverage sequencing became available. However, no functional or medical information is being collected. The potential of the 1000 Genomes Project for pharmacogenomics has been emphasized before (Gamazon et al., 2009). To illustrate how 1000 Genomes data may be used in pharmacogenetics for fine analysis, e.g., in search for causal variants, Figure 1 shows exemplarily the contribution of new SNP information to the genomic region of CYP3A flanking the CYP3A5*3 SNP rs776746 (±250 kb). While in the HapMap data (Figure 1A) only eight SNPs were in strong linkage to rs776746, 49 SNPs from current 1000 Genomes dataset were identified to be in strong LD, and interestingly also some moderately linked SNPs are located within CYP3A4 (Figure 1B). Unfortunately, linkage information of SNPs with potential functional impact within the CYP3A4 gene, like *1B or *22, is not available from both datasets, probably due to missing frequency data.
Table 2. Overview of databases providing valuable SNP/mutation data.
Figure 1. Increase of SNP data information by the 1000 Genomes Project within the CYP3A locus. LD-plots are generated for rs776746 using SNAP (http://www.broadinstitute.org/mpg/snap/ldplot.php); 250 kb region up- and downstream of the target SNP; genes are marked by green arrows, SNPs are shown with their R2-square values calculated versus the target SNP rs776746 (red squares) and recombination rates are given in cM/Mb (blue line); dashed lines mark the threshold for strong linkage R2 = 0.8 (horizontal) and the corresponding region of linked SNPs (vertical); (A) HapMap3 Release 2, CEU (B) 1000 Genomes Pilot 1, CEU.
For the CYP3A4 gene the current 1000 Genomes database release (Integrated Phase 1 Variant Set; May 2012) contains in total 471 SNPs assigned to the major transcript (ENST00000336411), including NCBI dbSNP database content (build 134). The 1000 Genomes Project to date (accessed September 2012) contributed 129 new SNPs to this collection. Besides 115 intronic variant positions 7 non-synonymous amino acid changes were previously unknown, of which four variants were reported on the CYPallele homepage (*4, *8, *11, *21) and only one was predicted to be deleterious by phenotype prediction tools SIFT and PolyPhen (Table 3). However, for most of the SNPs, availability of global MAF and population frequency data is still limited. Although most of the novel variants are rare, it should be noted that these can collectively make a marked contribution to the functional population variability. For individual patients, the combination of a rare deleterious variant with more frequent alleles of low function (compound heterozygosity) can be of predictive value. This was for example demonstrated for the polymorphic CYP2B6 in a large clinical study with HIV patients under efavirenz treatment. It was shown that several individuals with elevated efavirenz plasma concentrations could be predicted when rare variants were considered together with the common low-expressor *6-allele (Rotger et al., 2007). Taking this into account, the knowledge on genetic variability of ADME (Absorption Distribution Metabolism Excretion) genes including CYP3A4 in diverse populations will profit enormously from 1000 Genomes and new candidate SNPs influencing CYP3A4 expression and activity will certainly be discovered, although prediction or experimental testing of functional impact of the many novel variants pose a challenging task.
Table 3. CYP3A4 coding SNPs provided by the 1000 Genomes Project (selected are the SNPs for the major transcript ENST00000336411 from http://browser.1000genomes.org/Homo_sapiens/Search/Results?site=ensembl&q=cyp3a4) accessedSeptember 2012.
Genes Influencing CYP3A4 Phenotype Outside the CYP3A Locus
Regulation of CYP3A4 phenotype expression is enormously complex including influences from networks of nuclear receptors and other transcription factors (Pascussi et al., 2008), hormonal and inflammatory pathways (Aitken et al., 2006), heme and protein synthesis, and degradation pathways, as well as components of monooxygenase complexes and their interaction partners (see in Figure 2). Potentially influential polymorphisms in these genes on CYP3A4 expression have been studied only in recent years by single gene or pathway-directed approaches.
Figure 2. Regulation network of CYP3A4 phenotype expression adapted from Klein et al. (2012). The scheme displays the promoter region of CYP3A4 covering constitutive liver enhancer module CLEM4, xenobiotic responsive enhancer module XREM, and the proximal promoter prP. Genes of the constitutive and inducible pathways (Jover et al., 2002; Burk and Wojnowski, 2004) drug transporters, inflammatory signaling (Martínez-Jiménez et al., 2005; Aitken et al., 2006), possible miRNA interference (Pan et al., 2009), and of the heme biosynthesis/metabolism pathway as well as potential electron donors are listed. Genes with documented influential polymorphisms on CYP3A4 expression are depicted in red. Abbreviations: ALAS1, δ-aminolevulinate-synthase; ARNT, aryl hydrocarbon receptor nuclear translocator; CAR, constitutive androstane receptor; c/EBP, CCAAT/enhancer binding protein-α; Coup-TFII, COUP transcription factor II; CyB5, cytochrome B5; CYP3A4, cytochrome P450 3A4; FXR, farnesoid X-receptor; GR, glucocorticoid receptor; HMOX, heme-oxygenase; HNF1α, hepatocyte nuclear factor 1 homeobox A; FoxA2 (HNF3β), forkhead box A2; FoxA3 (HNF3Γ), forkhead box A3; HNF4α, hepatocyte nuclear factor 4 α; IL1β, interleukin-1 β; IL1RN, interleukin-1 receptor antagonist; IL6, interleukin-6; IL6R, interleukin-6 receptor; IL6ST, interleukin-6 signal transducer; LRH1, liver receptor homolog 1; LXRα/β, liver X-receptor; MDR, multi-drug resistance protein; NF-κB, nuclear factor-κB subunits; PGRMC, progesterone receptor membrane component; POR, P450 oxidoreductase; PPARα, peroxisome proliferator-activated receptor α; RARα, retinoic acid receptor; RXRα, retinoid X-receptor; PXR, pregnane X-receptor; SHP, short heterodimer partner; SLCO, solute carrier organic anion transporters; USF-1, upstream stimulatory factor 1; VDR, vitamin D receptor.
NADPH:cytochrome P450 oxidoreductase (POR) is a microsomal flavoprotein and an obligatory electron donator in the microsomal P450 monooxygenase reaction. In contrast to the multiplicity of CYPs, mammals have only a single POR gene. In humans the gene is located on chromosome 7q11.2 and spans about 72 kb, coding for a 680 amino acid protein. Complete deletion of the por gene in mouse is embryonically lethal most likely due to deficient adrenocortical steroidogenesis (Shen et al., 2002; Otto et al., 2003). In contrast, liver-specific por knockout leads to phenotypically and reproductively normal mice that accumulate hepatic lipids and have a drastically diminished capacity for hepatic drug metabolism (Gu et al., 2003; Finn et al., 2007).
The amount of POR in human liver is stoichiometrically ∼5- to 10-fold lower compared to the microsomal CYP pool, and hepatic POR levels are correlated to several P450 monooxygenase activities, suggesting that it represents a limiting factor (Huang et al., 2008a; Gomes et al., 2009). Functional polymorphisms in POR should thus be expected to influence CYP activity. In recent years rare POR missense mutations in humans were discovered that impair POR function and cause disordered steroidogenesis, ambiguous genitalia, and Antley–Bixler syndrome (Flück et al., 2004; Flück and Pandey, 2011). The CYPalleles website currently lists 41 distinct star-alleles, most of which represent very rare mutations, but common polymorphisms also exist (Huang et al., 2005, 2008a).
In particular the A503V variation (POR*28) is common with frequencies ranging from 19 to 37% in all major ethnicities. In recombinant systems the variant retained >50% of the wild type activity toward several CYPs (Huang et al., 2008b; Sandee et al., 2010) and CYP3A4 activity was influenced in a substrate-dependent way (Agrawal et al., 2010). In an in vivo study it was found that POR*28 TT genotype was associated with a 1.6-fold increase in CYP3A midazolam 1′-hydroxylase activity compared with POR*28 C carriers, a finding that could be replicated in an independent cohort (Oneda et al., 2009). Similarly, in a cohort of allograft recipients under tacrolimus therapy, POR*28 T-allele carriers had significantly higher tacrolimus dose requirements compared to non-carriers but only if they were genotypic CYP3A5 expressors (i.e., presence of at least one CYP3A5*1 allele; De Jonge et al., 2011). Thus, the effect of this common POR variant appears to depend on the CYP isozyme as well as the substrate.
Numerous additional genetic POR variants have been identified (Hart et al., 2008; Huang et al., 2008a). With regard to CYP3A4, several variants were described to affect its function in liver, in vitro or in vivo. A multivariate analysis in human liver microsomes identified three intronic POR variants that affected several CYP activities and that accounted for 60% of the microsomal atorvastatin hydroxylase variability, in concert with the donor’s sex (Gomes et al., 2009). Chen et al. analyzed six full length protein variants for their impact on CYP3A4-mediated testosterone hydroxylation and on CYP2B6-mediated bupropion hydroxylation in a recombinant system. Several POR variants showed markedly differential effects on both activities (Chen et al., 2012). In vivo, reduction in hepatic drug metabolizing CYP3A4 activities caused by POR mutations was also described in patients with disordered steroid metabolism (Flück et al., 2010). Taken together these recent advances indicate that POR variants are a complex but potentially relevant source of genetic variation for CYP3A-related drug oxidation phenotypes (Miller et al., 2011).
The xenosensors pregnane X-receptor (PXR, NR1I2) and constitutive androstane receptor (CAR, NR1I3) are important transcription factors in the regulatory network of CYP3A4 constitutive and inducible expression. Both genes are polymorphic and genetic variants have been studied for impact on CYP3A4 transcription (Lamba et al., 2005). Despite existence of numerous alternative transcripts, naturally occurring functional polymorphisms of CAR that contribute to CYP3A4 phenotypic expression are not well documented. In contrast, the functional impact of genetic PXR variants has been studied more thoroughly. For example, the protein variants V140M, D163G, and A370T, discovered in an exon sequence screening of PXR gene in DNA samples of several ethnicities, were shown to exhibit altered basal or induced transactivation activity of CYP3A4 promoter using recombinant variant expression and promoter-reporter constructs (Hustert et al., 2001b). Resequencing analysis of 46 liver tissue samples of Caucasian origin and hepatocytes identified SNPs in the PXR promoter and intron 1 associated with CYP3A4 mRNA expression, mainly due to destruction of putative transcription factor binding sites within the regulatory region of PXR by polymorphisms in strong linkage (Lamba et al., 2008). Moreover, the PXR*1B haplotype, which is tagged by the SNPs 2654T > C and IVS6-17C > T, was related to doxorubicin clearance in Asian breast cancer patients (Sandanaraj et al., 2008). Further studies analyzing patient cohorts under fosamprenavir/lopinavir or artemisinin treatment gave additional hints to some PXR variants that may affect inducibility of CYP3A4 phenotype expression (Svärd et al., 2010; Piedade et al., 2012). The occurrence of two SNPs in the 3′UTR region of PXR, rs3732359 and rs3732360, has been shown to be associated with altered midazolam 1′-hydroxylation in a liver bank and with more pronounced effect in midazolam clearance of healthy volunteers of African American descent (Oleson et al., 2010). Two recent studies included PXR polymorphisms in their pathway targeted pharmacogenetic approach on variable CYP3A4 expression in liver samples (Lamba et al., 2010; Klein et al., 2012). Although in the former study PXR rs1523130 was significantly associated with CYP3A4 mRNA expression by univariate analysis and in the multivariate model, the latter study did not document a significant contribution of PXR SNPs in univariate as well as in multivariate statistical models on mRNA, protein or activity. In summary, contribution of PXR variants to CYP3A4 expression remains controversial and may be limited and dependent on the population studied.
Based on the observation that CYP3A4 and the multi-drug resistance protein P-glycoprotein [P-gp, product of the MDR1 (ABCB1) gene] display largely overlapping substrate selectivity (Wacher et al., 1995; Patel and Mitra, 2001; Pal and Mitra, 2006), it has been hypothesized that changes in P-gp expression may influence the intracellular concentration of endogenous or exogenous substances that potentially lead to CYP3A4 induction, thus contributing to CYP3A4 expression differences (Lamba et al., 2006). Although data supporting this hypothesis have been reported in one human liver association study (Lamba et al., 2010), they were not reproduced in another study (Klein et al., 2012).
In search for additional influential genes, Lamba et al. (2010) phenotyped 128 livers by quantitative real-time PCR for expression of CYP3A genes and identified a functional CCT-repeat polymorphism in the FoxA2 (HNF3α) gene to be associated with higher expression of FoxA2 mRNA and its target genes PXR and CYP3A4. Polymorphisms in FoxA2, HNF4α, FoxA3 (HNF3Γ), PXR, MDR1, and the CYP3A4 promoter together with sex explained 24.6% of the variation in hepatic CYP3A4 mRNA expression. However the study lacked information on the relevance of these variations for CYP3A4 protein and activity.
More recently, we carried out extensive candidate gene approaches on 150 Caucasian liver samples phenotyped for CYP1A2 and CYP3A4 mRNA and protein levels, as well as enzyme activity (Klein et al., 2010, 2012). With respect to CYP3A4, we identified SNPs in the Ah-receptor nuclear translocator (ARNT), glucocorticoid receptor (GR), progesterone receptor membrane component 2 (PGRMC2), and peroxisome proliferator-activated receptor alpha (PPARA) to be consistently associated with CYP3A4 phenotype in human liver in the multivariate analysis. Validation in an atorvastatin-treated volunteer cohort confirmed decreased atorvastatin-2-hydroxylation in carriers of PPARA SNP rs4253728. Moreover, homozygous carriers of the variant had reduced PPARα protein expression in liver, and shRNA-mediated PPARA gene knock-down in primary human hepatocytes decreased mRNA expression levels of CYP3A4 by more than 50%. Multivariate analysis revealed that two linked PPARA SNPs alone explained ∼8–9% of the atorvastatin hydroxylase activity variation, whereas all genetic and non-genetic factors together accounted for ∼33% of atorvastatin 2-hydroxylase variation in this liver cohort (Klein et al., 2012). This result was somewhat unexpected, because PPARα had so far not been considered as a major regulator of CYP3A4, although inducing effects by fibrates had been noted before in human, but not mouse primary hepatocytes (Prueksaritanont et al., 2005; Rakhshandehroo et al., 2009). The interesting question of course is, whether CYP3A4 is a direct target of PPARα or whether indirect regulation, e.g., via nuclear receptor crosstalk resulting in downregulation of PXR (Aouabdi et al., 2006; Takagi et al., 2008) is the causative mechanism. Recent data from our group suggest, however, that PPARα indeed binds to several non-consensus PPARα-response elements (PPREs) in the CYP3A4 promoter to activate transcription in a ligand-dependent manner (Thomas et al., 2013). Because PPARα is a master regulator of lipid homeostasis and energy balance, these results indicate a novel connection between endogenous and xenobiotic metabolism.
New Aspects/Outlook
Several genome-wide association studies with a total number of over 1000 human liver samples identified a large number of novel expression quantitative trait loci (eQTL) for numerous liver-expressed genes (Schadt et al., 2008; Yang et al., 2010; Innocenti et al., 2011; Schröder et al., 2013). Although the advantage of this approach is the unbiased way of investigation, results were rather disappointing with respect to CYPs, probably due to lack of statistical power. Thus, mainly polymorphisms in CYP2D6 and CYP3A5 were reproduced in these studies (Schadt et al., 2008; Schröder et al., 2013). Building up on one eQTL study, Yang et al. used the genome-wide SNP data of 466 livers to search for associations with enzyme activities determined for 9 CYPs (i.e., activity- or aQTLs). A total of 54 SNPs influencing 8 CYP activities were identified, of which 30 influenced CYP2D6 in cis (i.e., SNPs were located within ±1 Mb of the CYP2D6 gene), whereas all remaining 24 SNPs were described as trans-acting elements, and only one of these (rs12041966 located on chromosome 1) influenced testosterone hydroxylation (Yang et al., 2010). Unfortunately, functional annotation of the trans-acting SNPs was not possible in this study, and these results thus await further experimental confirmation.
A further level of potential importance, which has not yet been explored in terms of genetic variability concerns the influence of epigenetic processes on pharmacologically relevant genes and drug response (Gomez and Ingelman-Sundberg, 2009). SNPs in DNA methylation regions or miRNAs and miRNA binding sites, as well as miRNA copy number variations may influence target gene expression (Schmeier et al., 2011). Thus, CYP3A4 expression was shown to be directly regulated by miRNAs but can also be influenced indirectly by miRNA regulation of transcriptional regulators such as PXR and VDR (Pan et al., 2009). However, polymorphic variation within this regulatory pathway has not yet been analyzed. Furthermore, additionally to regulatory polymorphisms (rSNPs) affecting transcription, structural RNA polymorphisms (termed srSNPs) are suggested to influence RNA function (splicing, turnover, translation) and to display promising biomarkers (Sadee et al., 2011; Lee et al., 2012).
The ENCODE project (ENCyclopedia Of DNA Elements)5 systematically analyzes functional DNA elements in the human genome (e.g., binding data for more than 100 transcription factors, DNAse sensitive sites, methylation, chromatin interaction, and genotyping from multiple cell types) and may provide new hypotheses on functional consequences of SNPs located especially in non-coding DNA-regions (Bernstein et al., 2012; Gerstein et al., 2012; Yip et al., 2012).
In conclusion, the predictive power of currently known genetic polymorphisms with relevance for CYP3A4 in vivo phenotype is still far away from the expected 60–80% of genetic determination. The use of next generation sequencing approaches for the identification of causal variants in CYP3A4 as well as the numerous genes of its many influential pathways may lead to the identification of many more rare and common DNA variants that together account for a sizeable fraction of this variability. The examples of POR and PPARA demonstrate that CYP3A4 variability is at least in part determined by polymorphisms in genes outside the CYP3A4 locus. However, investigating and validating trans-acting factors is much more difficult due to the more indirect nature of interaction which is more likely to be masked by covariates, thus necessitating larger studies, in vitro or in vivo. In addition, mathematical algorithms are needed to combine many genetic variants, some of which contribute only small fractions to the total variability, into practically useful signatures for application on clinical studies and individualized medicine.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
Work in the authors’ laboratory was supported by the German Federal Ministry of Education and Research (Virtual Liver Network grant 0315755), the 7FP EU Initial Training Network program‚ FightingDrugFailure’ (GA-2009–238132), and by the Robert-Bosch Foundation, Stuttgart, Germany.
Footnotes
References
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Keywords: cytochrome P450, CYP3A4, pharmacogenomics, pharmacogenetics, drug metabolism, heritability
Citation: Klein K and Zanger UM (2013) Pharmacogenomics of cytochrome P450 3A4: recent progress toward the “missing heritability” problem. Front. Genet. 4:12. doi: 10.3389/fgene.2013.00012
Received: 18 October 2012; Accepted: 26 January 2013;
Published online: 25 February 2013.
Edited by:
José A. Agúndez, University of Extremadura, SpainReviewed by:
Elena García-Martín, Universidad de Extremadura, SpainEric Gamazon, University of Chicago, USA
Copyright: © 2013 Klein and Zanger. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
*Correspondence: Kathrin Klein, Dr. Margarete Fischer Bosch Institute of Clinical Pharmacology, Auerbachstr. 112, 70376 Stuttgart, Germany. e-mail: kathrin.klein@ikp-stuttgart.de