- Research article
- Open Access
UDP-glucuronosyltransferase and sulfotransferase polymorphisms, sex hormone concentrations, and tumor receptor status in breast cancer patients
Breast Cancer Research volume 6, Article number: R488 (2004)
UDP-glucuronosyltransferase (UGT) and sulfotransferase (SULT) enzymes are involved in removing sex hormones from circulation. Polymorphic variation in five UGT and SULT genes – UGT1A1 ((TA)6/(TA)7), UGT2B4 (Asp458Glu), UGT2B7 (His268Tyr), UGT2B15 (Asp85Tyr), and SULT1A1 (Arg213His) – may be associated with circulating sex hormone concentrations, or the risk of an estrogen receptor-negative (ER-) or progesterone receptor-negative (PR-) tumor.
Logistic regression analysis was used to estimate the odds ratios of an ER- or PR- tumor associated with polymorphisms in the genes listed above for 163 breast cancer patients from a population-based cohort study of women in western Washington. Adjusted geometric mean estradiol, estrone, and testosterone concentrations were calculated within each UGT and SULT genotype for a subpopulation of postmenopausal breast cancer patients not on hormone therapy 2–3 years after diagnosis (n = 89).
The variant allele of UGT1A1 was associated with reduced risk of an ER- tumor (P for trend = 0.03), and variants of UGT2B15 and SULT1A1 were associated with non-statistically significant risk reductions. There was some indication that plasma estradiol and testosterone concentrations varied by UGT2B15 and SULT1A1 genotypes; women with the UGT2B15 Asp/Tyr and Tyr/Tyr genotypes had higher concentrations of estradiol than women with the Asp/Asp genotype (P = 0.004). Compared with women with the SULT1A1 Arg/Arg and Arg/His genotypes, women with the His/His genotype had elevated concentrations of testosterone (P = 0.003).
The risk of ER- breast cancer tumors may vary by UGT or SULT genotype. Further, plasma estradiol and testosterone concentrations in breast cancer patients may differ depending on some UGT and SULT genotypes.
Exposure to increased concentrations of both estrogens and androgens has been implicated in the development of breast cancer [1–3]. There are varied mechanisms by which sex hormones might act to propagate malignancy; at the same time, there are only a few pathways by which these hormones are inactivated and removed from circulation. Glucuronidation and sulfonation are two of the pathways through which sex hormones can be metabolized to inactive compounds [4–6].
Glucuronidation is catalyzed by UDP-glucuronosyltransferase (UGT) enzymes and involves the covalent addition of glucuronic acid, resulting in more hydrophilic compounds that are excreted from the body via urine or bile [6, 7]. UGT1A1, UGT2B4, UGT2B7, and UGT2B15 are among the UGT enzymes that metabolize steroid hormones .
The UGT1A1 protein glucuronidates estriol, 17β-estradiol, ethinylestradiol, and catechol estrogens [8–11]. Variation in glucuronidation between individuals is due primarily to a variable number of TA repeats in the A(TA) n TAA (n = 5–8) promoter sequence in the TATA-box region [12, 13]. Among the variant alleles, (TA)7 (the most common variant) and (TA)8 are associated with lower transcriptional activity in vitro than the (TA)6 wild-type allele [12–14]. An increasing number of TA repeats has been associated with increased breast cancer risk in premenopausal African-American women, but not postmenopausal African-American or premenopausal or postmenopausal Caucasian women [14, 15].
The UGT2B4 enzyme glucuronidates catechol estrogens, estriol, and bile acids [16–18]. A polymorphism in the UGT2B4 gene (Asp458Glu) has been reported . The two alleles have similar tissue distributions and currently there is little biochemical evidence to suggest different substrate specificities between the two isoforms [16, 19]. However, it has not yet been determined whether this polymorphism affects UGT2B4 protein function through other mechanisms. The UGT2B7 enzyme glucuronidates a wide variety of steroids, including catechol estrogens, estriol, and hydroxylated androgens [10, 17, 18, 20–25]. A polymorphism in the UGT2B7 gene results in an amino acid change (His268Tyr) , possibly near the proposed substrate-binding site of the protein [22, 26]. The two alleles seem to have similar enzymatic activities for most substrates [10, 24, 27], with the possible exception of androsterone, estriol, and estradiol [21–23, 25]. The UGT2B15 enzyme conjugates catechol estrogens and the C19 sex steroids testosterone, dihydrotestosterone, and androstane-3α, 17β-diol [18, 28–30]. A polymorphism in the UGT2B15 gene (Asp85Tyr)  results in an allele with a Vmax for androstane-3α, 17β-diol and dihydrotestosterone in vitro that is double that of the aspartic acid allele .
Sulfotransferases (SULTs) comprise another group of enzymes involved in the removal of circulating bioactive sex hormones. The SULT1A1 enzyme can catalyze the sulfonation of estrogens to form inactive estrogen sulfates [6, 31, 32]. It has been proposed that estrone sulfate serves as an inactive reservoir in the blood from which estrone and estradiol can be regenerated [6, 33]. A polymorphism in the SULT1A1 gene (Arg213His) has been identified . Individuals homozygous for the histidine allele have lower platelet SULT activity in vitro than wild-type and heterozygous individuals [34, 35]. Further, the SULT1A1 variant allele is associated with an elevated breast cancer risk among postmenopausal women .
Because the UGT and SULT enzymes are important in the inactivation and removal of bioactive sex hormones from target tissues, investigating the association between polymorphisms in these genes and circulating sex hormone concentrations might help to elucidate the potential functional relevance of these polymorphisms in vivo. These observations might support experimental results suggesting a functional role for polymorphisms in UGT1A1, UGT2B15, and SULT1A1, or might generate new hypotheses about the potential effect of sequence variations in UGT2B4 and UGT2B7, for which there is relatively little biochemical evidence suggesting a functional effect in vitro. With this purpose we investigated the association between these polymorphisms and circulating sex hormone concentrations in postmenopausal breast cancer patients not taking hormones 2–3 years after diagnosis. In view of increasing evidence that hormones are important in the development of hormone-dependent and hormone-independent breast cancer tumors [37–41], we also examined the association between polymorphisms in the UGT1A1, UGT2B4, UGT2B7, UGT2B15, and SULT1A1 genes and breast tumor estrogen receptor (ER) and progesterone receptor (PR) status in newly diagnosed breast cancer patients.
Materials and methods
The Health, Eating, Activity, and Lifestyle (HEAL) study is a population-based, multicenter prospective cohort study in which women with breast cancer are followed to determine whether breast cancer prognosis is associated with diet, physical activity, sex hormones, weight, or other exposures . Participants in the HEAL study were identified through Surveillance, Epidemiology, and End Results (SEER) registries in western Washington state, in New Mexico, and in Los Angeles County, California. The analyses presented here are limited to breast cancer cases in Washington state who were identified through the western Washington SEER cancer registry between 1996 and 1999. To be eligible, women had to be newly diagnosed with stage 0, I, II, or IIIa breast cancer, living in King, Pierce, or Snohomish counties, and to have clinic measurements and a blood draw within 4 to 12 months of diagnosis. Because the majority of women were either Caucasian or Asian, the analyses were restricted to these two races. Of 202 patients interviewed in western Washington, 184 women were Caucasian or Asian and had a blood draw at baseline. Of these women, the ER and PR status of the breast tumor was determined for 163 women. Women for whom ER and PR status were determined did not significantly differ from the 21 women with unknown receptor status with respect to characteristics presented in Table 1, with the exception that the latter women were more likely to have in situ breast cancer (31% versus 52%). A participant's menopausal status was determined by using self-reported information on estrogen and tamoxifen use, prior ovarian surgery or hysterectomy, menstrual history, and measured values of estrone, estradiol, and follicle-stimulating hormone. At baseline, 61 women were classified as premenopausal, 98 as postmenopausal and 4 were unable to be classified. Data from a follow-up interview and blood draw that occurred 24 months after initial enrollment were used for the analysis of serum hormone concentrations. At the 24-month follow-up, 35 women were classified as premenopausal, 114 as postmenopausal, and 16 were unable to be classified. Because we were unable to collect blood samples from premenopausal women at the same point in the menstrual cycle, hormone analyses were limited to postmenopausal Caucasian and Asian women who had complete data for estrone, estradiol, height and weight, and who were not taking estrogen or progesterone replacement hormones at the time of the blood draw (n = 89). There was no correlation between hormone concentrations and time from breast cancer diagnosis to blood draw at the 24-month follow-up.
Written informed consent was obtained from each participant. The protocol was approved by the Institutional Review Board of the Fred Hutchinson Cancer Research Center.
Data from two time points were used in this study. The first time point was the time of study enrollment, 4–12 months after breast cancer diagnosis. The second time point was about 24 months after study enrollment. Patients were mailed study questionnaires to complete and bring with them to their clinic evaluations at the Fred Hutchinson Cancer Research Center Prevention Studies Clinic. Information was collected on the following: dietary intake; health habits; reproductive and menstrual history; history of use of oral contraceptives and hormone replacement therapy; medical history, including history of endocrine problems and other medical problems; history of benign breast disease; family history of breast cancer, other cancers, and diabetes mellitus; history of tobacco, caffeine, and alcohol use; lifetime weight patterns; detailed current and pre-diagnostic physical activity habits; mammographic screening; and selected demographic data. Standard height and weight measurements were obtained by trained staff during home or clinic visits. Percentage body fat was measured by bioelectric impedance (RJL Multifrequency Bioelectric Impedance Analyzer, Clinton Township, MI). Bioelectrical impedance measurements were made with standard electrode placements after a minimum 4-hour fast.
A 30 ml fasting blood draw was collected at the 24-month follow-up visit to determine circulating concentrations of sex hormones. Blood was processed within 1 hour of collection; serum, plasma, and buffy coat aliquots were stored at -70 to -80°C. Dates of sample collection and processing, time of day of blood collection, and time since last meal were recorded.
Estrone and estradiol assays were performed at Quest Diagnostics Nichols Institute (San Juan Capistrano, CA) between July and August 2001. The testosterone assay was performed in Dr Frank Stanczyk's laboratory at the University of Southern California between April and June 2002. Samples were assigned randomly to assay batches and ordered randomly within each batch. Laboratory personnel performing the assays were blinded to subject identity.
Estrone and estradiol assay methods consisted of organic solvent extraction, followed by Celite column partition chromatography before quantification by radioimmunoassay. The reported sensitivities of these assays are less than 10 pg/ml and less than 2 pg/ml, respectively. Testosterone was also measured by extraction, Celite column chromatography, and radioimmunoassay; this method has a sensitivity of 1 ng/dl. Twenty replicated samples and eight pooled quality-control samples (two samples per batch) were included in the estrone and estradiol blood assays. For estrone and estradiol, the intra-assay coefficients of variation (CVs) were 13.3% and 28.8%, respectively, and the total CV results were 13.3% and 29.1%, respectively. For testosterone, 20 replicated samples and 14 pooled quality-control samples (two samples per batch) were included in the blood assays. The intra-assay CV and total CV were both 9.6%. Four subjects had estrone measurements below the 10 pg/ml limit of detection. To calculate a representative estrone value for measurements below this detection limit, we fitted a truncated log-normal distribution to the observed estrone data. The truncation was considered at the lower end of the distribution and the cumulative proportion at the truncation point (namely, estrone = 10 pg/ml) was used as the likelihood contribution from each of the subjects with estrone below the detection limit. The maximum likelihood estimate of the mean of the lognormal distribution was 3.079 and that of the standard deviation was 0.453. Using these maximum likelihood estimates in the lognormal distribution, we calculated the mean estrone value less than 10 pg/ml to be 8.702 pg/ml. The four estrone measurements below the limit of detection were assigned this value.
Hormone receptor characterization
Paraffin-embedded breast tumor tissue samples from 163 women were tested for this study. ER and PR proteins were assessed by immunohistochemistry in a single laboratory without knowledge of other laboratory results, patient characteristics, or outcome. Tissue blocks were selected by reviewing all histologic slides for each case. Blocks for testing were selected for the presence of representative tumor and, when available, the presence of adjacent benign epithelium (used as an internal positive control). Immunohistochemistry was performed with modified standard immunohistochemical techniques. In brief, 5 μm sections of tumor were cut onto glass slides and blocked for endogenous peroxidase. Slides were treated with microwaves in the presence of citrate buffer [43–45]. After washes, primary antibodies (monoclonal anti-PR clone 1A6 [NovoCastra Lab] [46, 47] and monoclonal anti-ER clone ER1D5 [AMAC, Inc.]) [48–50] were applied to the sections and incubated for 1 hour. Slides were washed and appropriate biotinylated secondary antibody, diluted in accordance with the manufacturer's instructions (Vector Laboratories, Burlingame, CA), was applied for 30 minutes. Slides were incubated for 30 minutes with avidin–biotin complex, followed by diaminobenzidine with 8% NiCl2 for 10 minutes; nuclei were counterstained with methyl green [51, 52]. Tumor cells were scored positive if nuclear immunostaining was present and more than 5% of tumor cells had positive staining.
A 50 ml fasting blood draw was collected at the time of the baseline interview. Blood was processed into serum, plasma, and buffy coat fractions and aliquots were stored at -70 to -80°C. DNA for genotyping was extracted from the buffy coat fraction at the Core Specimen Processing Laboratory (Fred Hutchinson Cancer Research Center) with standard techniques.
SULT1A1 genotyping of the Arg213His polymorphism was performed with a restriction-fragment-length polymorphism assay. A SULT1A1-specific fragment containing the polymorphism was amplified in a 20 μl reaction containing 1 × GeneAmp buffer II (Applied Biosystems, Foster City, CA), 3 mM MgCl2, 200 μM deoxynucleotide triphosphates, each primer at 200 nM (forward primer 5'-AGTTGGCTCTGCAGGGTTTCT-3', reverse primer 5'-ACCACGAAGTCCACGGTCTC-3'), 100 ng of genomic DNA, and 0.5 U of AmpliTaq DNA polymerase (Applied Biosystems). Cycling was as follows: initial denaturation at 94°C for 5 minutes, followed by 35 cycles of 94°C for 30 seconds, 59°C for 45 seconds, and 72°C for 45 seconds, and final extension at 72°C for 5 minutes. The amplified fragment was digested with HhaI and separated on a 2% NuSieve agarose gel (Cambrex, Rockland, ME). The fragment sizes were 160 and 40 base pairs for the wild-type allele, and 200 base pairs for the variant allele. For quality control purposes, genotyping was repeated for 10% of the samples for each genotype. There were no discrepancies between the two results. UGT2B4 Asp458Glu, UGT2B7 His268Tyr, UGT2B15 Asp85Tyr, and UGT1A1 [TA] n genotyping was performed as described previously [53, 54].
We addressed two separate research questions, using two different statistical models. We first examined whether genotype was related to the risk of developing an ER-negative (ER-) or PR-negative (PR-) breast cancer tumor. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated by using unconditional logistic regression analysis to evaluate the association between genotype and tumor receptor status. We adjusted our logistic regression analyses for variables for which we had a priori knowledge of potential contribution to breast cancer risk or to the development of hormone-dependent or hormone-independent breast tumors. Because of the small size of the study, the data were not sufficiently robust to employ specific methods to evaluate confounding. In addition to race (Caucasian/Asian), the following breast cancer risk factors were included as covariates in the analysis: age at the time of interview (continuous), age at menarche (continuous), number of ovaries remaining, number of pregnancies lasting at least 6 months (0, 1, 2, or 3 or more), menopausal status at time of baseline interview (premenopausal/postmenopausal), smoker at time of interview (yes/no), parity/age at first birth (nulliparous, age at first birth 26 or less, age at first birth more than 26), change in weight from age 18 to the age that the subject had most recently passed (35, 50, or 60 years old). Eight of the 163 women were excluded from the logistic regression analyses because of missing covariate data, leaving 155 women in the final model. Genotype indicator variables were created by using the wild-type genotype as the reference category in the regression models. Genotypes were also evaluated with dichotomous variables ('any wild-type allele' [wild-type and heterozygous individuals] versus homozygous variant individuals, and 'any variant allele' [heterozygous and homozygous variant individuals] versus wild-type individuals) when patterns suggested a dominant or recessive genotype effect, respectively. We evaluated menopausal status as a potential effect modifier but were unable to evaluate effect modification by race owing to small numbers. However, we modeled effects excluding Asian women to evaluate whether results were different when limited to Caucasian women. All logistic regression analyses were performed with SAS statistical software, version 8.2 (SAS Institute, Cary, NC).
Our second research question examined whether genotype was related to sex hormone concentrations. Linear regression analysis with robust variance estimates was used to evaluate the association between UGT and SULT genotypes and circulating sex hormone concentrations (estrone, estradiol, testosterone) in postmenopausal women not taking estrogen or progesterone replacement hormones at the time of the blood draw. Hormone concentrations were natural-logarithm transformed to approximate normal distributions. We adjusted the linear regression analyses for variables for which we had a priori knowledge of potential contribution to sex hormone concentrations. Geometric mean hormone concentrations within each genotype were calculated after adjustment for age at the time of interview (continuous), percentage body fat (continuous), tamoxifen use at the time of blood draw (yes/no), alcohol use (yes/no), smoking (yes/no), number of ovaries remaining, race (Asian/Caucasian), and batch number (estrone and estradiol only). We evaluated tamoxifen use as a potential effect modifier. As with the logistic regression analyses, we evaluated whether restriction to Caucasian women altered the results. Of the 82 Caucasian and 7 Asian postmenopausal women with complete data for estrone, estradiol, height, and weight who were not taking estrogen or progesterone replacement hormones at the time of the blood draw, two were lacking body fat data and one was lacking data for plasma testosterone. These women were dropped from the multivariate linear regression analysis, resulting in 87 women with estradiol and estrone data, and 86 women with testosterone data. All linear regression analyses were performed with Stata statistical software, version 7 (Stata Corporation, College Station, TX).
A total of 163 women (150 Caucasian and 13 Asian) from Washington state were enrolled in the HEAL study and had complete baseline interview and hormone receptor data. Most women were diagnosed with Stage I breast cancer (51%) (Table 1), were postmenopausal at the time of study enrollment (60%), and had no known family history of breast cancer (51%). Most of these women had an ER-positive (ER+) or PR-positive (PR+) breast tumor and 66% had a combined ER+/PR+ tumor.
In Caucasians (n = 150), the observed variant allele frequencies of each gene were as follows: UGT1A1, (TA)7 = 0.31; UGT2B4, Glu458 = 0.24; UGT2B7, Tyr268 = 0.55; UGT2B15, Tyr85 = 0.56; SULT1A1, His213 = 0.38. These allele frequencies were similar to those in Caucasians in previous reports [13, 34, 53–56]. We did not calculate separate allele frequencies in Asians because of the small number of individuals (n = 13). In Caucasians, genotype frequencies for each gene did not deviate from Hardy–Weinberg equilibrium.
As shown in Table 2, the risk of an ER- breast tumor seemed smaller for individuals with the UGT1A1 variant allele (compared with (TA)6/(TA)6: OR (TA)6/(TA)7 = 0.6, 95% CI 0.2–1.3; OR (TA)7/(TA)7 = 0.0, 95% CI 0.0–0.5; P for trend = 0.03). Further, a reduced risk of an ER- tumor might be associated with the SULT1A1 variant allele (OR = 0.6, 95% CI 0.3–1.2) and the UGT2B15 homozygous variant genotype (OR = 0.4, 95% CI 0.1–1.2). The effects were similar when the sample was limited to Caucasian women (data not shown). Trends for UGT1A1, UGT2B7, UGT2B15, and SULT1A1 were generally similar among premenopausal and postmenopausal women (data not shown).
Among the subpopulation of women eligible for hormone analysis (n = 89; Table 1), most (62%) were taking tamoxifen, but very few were current smokers (n = 4). Among this subgroup, women with the UGT1A1 (TA)7/(TA)7 genotype had 58% higher geometric mean estradiol concentrations (P = 0.01) than women with the (TA)6/(TA)6 wild-type genotype (Table 3) and 71% higher geometric mean estradiol concentrations (P = 0.002) than the combined group of women with either the (TA)6/(TA)6 or the (TA)6/(TA)7 genotype (9.8 pg/ml, 95% CI 8.7–11.1 versus 16.8 pg/ml, 95% CI 12.6–22.5). Women with the UGT2B15 Asp/Tyr and Tyr/Tyr genotypes had 59% (P = 0.003) and 44% (P = 0.05) higher geometric mean estradiol concentrations than women with the Asp/Asp genotype, respectively (Table 3). When genotypes were combined, women with any Tyr85 allele had 53% higher geometric mean estradiol concentrations than Asp/Asp wild-type women with no Tyr85 allele (P = 0.004; 7.2 pg/ml, 95% CI 5.6–9.4 versus 11.1 pg/ml, 95% CI 9.8–12.5). Finally, women with the SULT1A1 His/His genotype had 32% higher geometric mean testosterone concentrations than women with the wild-type Arg/Arg genotype (P = 0.03; Table 3), and 39% higher geometric mean testosterone concentrations than the combined group of women with the Arg/Arg or Arg/His genotype (P = 0.003; 26.4 ng/dl, 95% CI 24.3–28.7 versus 36.8 ng/dl, 95% CI 30.5–44.3). No statistically significant associations were observed between estradiol, estrone or testosterone concentrations and UGT2B4 or UGT2B7 genotypes. Results were similar when the analyses were restricted to Caucasians (data not shown). We did not observe that the relationship between any of the polymorphisms and circulating sex hormone concentrations differed between tamoxifen users and non-users (data not shown), but the small number of individuals within each subgroup limited our ability to observe a difference.
This study of female breast cancer patients had two aims: first, to evaluate the risk of ER- or PR- tumors associated with polymorphisms in specific UGT and SULT genes, and second, to investigate whether plasma sex hormone concentrations varied within genotypes of these same genes. To our knowledge this is the first study to investigate the association between polymorphisms in the UGT2B4, UGT2B7, and UGT2B15 genes and risk of an ER- or PR- breast tumor.
There is increasing evidence that hormones are important in the development of hormone-dependent and hormone-independent breast cancer tumors [37–41]. Women with ER- tumors have a worse prognosis and fewer treatment modalities are available. We observed a reduced risk of an ER- tumor in patients with the UGT1A1 (TA)7/(TA)7 genotype, and indications towards risk reduction with variants of UGT2B15 and SULT1A1. The association between breast tumor ER status and the number of TA repeats in the UGT1A1 promoter region has previously been examined in a case-control study of 200 African-American women with breast cancer . In that study, premenopausal women with (TA)7 and (TA)8 'low-activity' alleles seemed to be at higher risk for an ER- tumor than women with (TA)5 and (TA)6 'high-activity' alleles (OR = 2.1, 95% CI 1.0–4.2) . This elevated risk did not extend to postmenopausal women (OR = 0.8, 95% CI 0.3–1.9), which is consistent with our results among a predominantly postmenopausal population. Our finding of a somewhat reduced risk of an ER- or PR- tumor in women with the SULT1A1 Arg/His and His/His genotypes is consistent with the results of a study of 337 breast cancer patients by Nowell and colleagues . Given that the hormonal milieu seems important for the development of both hormone-dependent and hormone-independent mammary tumors, our study, in conjunction with others, provides evidence that genotypes relevant to the metabolism and excretion of sex hormones might affect that milieu.
In a substudy of postmenopausal women at least 2 years after diagnosis, we observed that plasma estradiol concentrations varied by UGT1A1 and UGT2B15 genotypes. The UGT1A1 gene is involved in the glucuronidation of several sex hormones, including 17β-estradiol [9, 11]. Our finding that breast cancer patients homozygous for the UGT1A1 variant (TA)7 allele seemed to have increased concentrations of estradiol is consistent with the observation that the variant allele has lower transcriptional activity in vitro than the wild-type (TA)6 allele [12–14]. However, a study of 274 healthy postmenopausal women in the Nurses' Health Study found that neither estrone nor estradiol concentration varied depending on UGT1A1 genotype . Our study was restricted to women with breast cancer, the majority of whom were on tamoxifen therapy, which alters estrogen levels, perhaps independently of these genetic factors. Our findings should therefore be confirmed in additional populations of breast cancer patients and healthy controls, to clarify the relationship between the UGT1A1 polymorphism and estradiol concentrations in both healthy women and those with breast cancer.
Our finding that concentrations of estradiol were higher in women with the UGT2B15 Tyr85 allele is surprising, given that the UGT2B15 protein is not known to glucuronidate estradiol [18, 29]. Further, we did not observe that circulating testosterone concentrations varied greatly by UGT2B15 genotype, despite the fact that UGT2B15 is known to glucuronidate testosterone [18, 29]. However, this might be explained by the much higher glucuronidation activity of UGT2B17 for testosterone than that of UGT2B15 [18, 58]. Also surprising was the finding that the SULT1A1 His/His genotype was associated with elevated testosterone concentrations, given that SULT1A1 does not seem to conjugate testosterone . It is possible that the observed associations between sex hormone concentrations and polymorphisms in UGT2B15 and SULT1A1 in breast cancer patients are valid. However, they should be viewed as possibly attributable to chance, because there are conflicting biochemical data reported in the literature.
With regard to the UGT2B4 and UGT2B7 polymorphisms, there was relatively little biochemical evidence to support an a priori hypothesis about an association between these polymorphisms and circulating sex hormone concentrations or tumor receptor status. We therefore considered these analyses to be 'hypothesis generating', in which any observed association might elucidate the potential functional relevance of these polymorphisms in vivo. We did not find evidence that these polymorphisms were associated with sex hormone concentrations or the risk of an ER- or PR- breast cancer tumor. Our findings therefore support in vitro data in which these sequence variations did not seem to alter enzyme function [10, 16, 24, 27].
Because genetic factors that might influence circulating sex hormone concentrations in breast cancer patients could influence response to treatment, it is important to understand these associations in breast cancer patients. The results of this study might serve as a starting point for the formation and testing of additional hypotheses regarding the potential association between polymorphisms in the UGT2B4, UGT2B7, and UGT2B15 genes and serum hormone concentrations or hormone receptor status. One strength of the study is the investigation of several genetic polymorphisms in genes relevant to sex hormone excretion or regulation and the measurement of three sex hormones.
However, this study has several limitations. The small size limited the statistical power in many of the analyses and prohibited the evaluation of combined genotype effects. Additionally, the coefficients of variation for the estrone and estradiol assays were somewhat high, possibly preventing us from detecting an association. Another limitation is that we examined polymorphisms in only five genes whose protein products participate in sex hormone regulation; additional proteins involved in regulatory mechanisms that contribute to sex hormone concentrations in vivo could not be considered as part of the study. As with any genetic association study, the results must be interpreted in the light of the possibility that observed associations might be due to linkage disequilibrium between the examined polymorphism and a functional polymorphism that is the true cause of the observed difference. Finally, because this study involved mostly overweight women with breast cancer, most of whom were taking tamoxifen at the time of the study, the observed associations between UGT and SULT genotypes and circulating hormone levels might not be generalizable to healthy women.
The results of this study of female breast cancer patients indicate that the risk of ER- tumors varies by UGT1A1, and possibly UGT2B15 and SULT1A1, genotype. Further, there was some indication that plasma estradiol and testosterone concentrations varied by UGT1A1, UGT2B15, or SULT1A1 genotype. Owing to the preliminary nature of these findings, they should be validated in a larger study population.
coefficient of variation
Health Eating, Activity, and Lifestyle
- SEER = Surveillance:
Epidemiology, and End Results
Key TJ: Serum oestradiol and breast cancer risk. Endocr-Relat Cancer. 1999, 6: 175-180.
Lillie EO, Bernstein L, Ursin G: The role of androgens and polymorphisms in the androgen receptor in the epidemiology of breast cancer. Breast Cancer Res. 2003, 5: 164-173. 10.1186/bcr593.
Endogenous Hormones and Breast Cancer Collaborative Group: Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies. J Natl Cancer Inst. 2002, 94: 606-616.
Radominska-Pandya A, Czernik PJ, Little JM, Battaglia E, Mackenzie PI: Structural and functional studies of UDP-glucuronosyltransferases. Drug Metab Rev. 1999, 31: 817-899. 10.1081/DMR-100101944.
Coughtrie MW: Sulfation through the looking glass – recent advances in sulfotransferase research for the curious. Pharmacogenomics J. 2002, 2: 297-308. 10.1038/sj.tpj.6500117.
Raftogianis R, Creveling C, Weinshilboum R, Weisz J: Estrogen metabolism by conjugation. J Natl Cancer Inst Monogr. 2000, 27: 113-124.
Mackenzie PI, Mojarrabi B, Meech R, Hansen A: Steroid UDP glucuronosyltransferases: characterization and regulation. J Endocrinol. 1996, 150: S79-S86.
Ebner T, Remmel RP, Burchell B: Human bilirubin UDP-glucuronosyltransferase catalyzes the glucuronidation of ethinylestradiol. Mol Pharmacol. 1993, 43: 649-654.
Senafi SB, Clarke DJ, Burchell B: Investigation of the substrate specificity of a cloned expressed human bilirubin UDP-glucuronosyltransferase: UDP-sugar specificity and involvement in steroid and xenobiotic glucuronidation. Biochem J. 1994, 303: 233-240.
Cheng Z, Rios GR, King CD, Coffman BL, Green MD, Mojarrabi B, Mackenzie PI, Tephly TR: Glucuronidation of catechol estrogens by expressed human UDP-glucuronosyltransferases (UGTs) 1A1, 1A3, and 2B7. Toxicol Sci. 1998, 45: 52-57. 10.1006/toxs.1998.2494.
King CD, Green MD, Rios GR, Coffman BL, Owens IS, Bishop WP, Tephly TR: The glucuronidation of exogenous and endogenous compounds by stably expressed rat and human UDP-glucuronosyltransferase 1.1. Arch Biochem Biophys. 1996, 332: 92-100. 10.1006/abbi.1996.0320.
Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP, Chowdhury NR: The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med. 1995, 333: 1171-1175. 10.1056/NEJM199511023331802.
Beutler E, Gelbart T, Demina A: Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?. Proc Natl Acad Sci USA. 1998, 95: 8170-8174. 10.1073/pnas.95.14.8170.
Guillemette C, Millikan RC, Newman B, Housman DE: Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans. Cancer Res. 2000, 60: 950-956.
Guillemette C, De Vivo I, Hankinson SE, Haiman CA, Spiegelman D, Housman DE, Hunter DJ: Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels. Cancer Epidemiol Biomarkers Prev. 2001, 10: 711-714.
Levesque E, Beaulieu M, Hum DW, Belanger A: Characterization and substrate specificity of UGT2B4 (E458): a UDP-glucuronosyltransferase encoded by a polymorphic gene. Pharmacogenetics. 1999, 9: 207-216.
Ritter JK, Chen F, Sheen YY, Lubet RA, Owens IS: Two human liver cDNAs encode UDP-glucuronosyltransferases with 2 log differences in activity toward parallel substrates including hyodeoxycholic acid and certain estrogen derivatives. Biochemistry (Mosc). 1992, 31: 3409-3414.
Turgeon D, Carrier JS, Levesque E, Hum DW, Belanger A: Relative enzymatic activity, protein stability, and tissue distribution of human steroid-metabolizing UGT2B subfamily members. Endocrinology. 2001, 142: 778-787. 10.1210/en.142.2.778.
Miners JO, McKinnon RA, Mackenzie PI: Genetic polymorphisms of UDP-glucuronosyltransferases and their functional significance. Toxicology. 2002, 181–182: 453-456. 10.1016/S0300-483X(02)00449-3.
Jin CJ, Mackenzie PI, Miners JO: The regio- and stereo-selectivity of C19 and C21 hydroxysteroid glucuronidation by UGT2B7 and UGT2B11. Arch Biochem Biophys. 1997, 341: 207-211. 10.1006/abbi.1997.9949.
Ritter JK, Sheen YY, Owens IS: Cloning and expression of human liver UDP-glucuronosyltransferase in COS-1 cells. 3, 4-catechol estrogens and estriol as primary substrates. J Biol Chem. 1990, 265: 7900-7906.
Jin C, Miners JO, Lillywhite KJ, Mackenzie PI: Complementary deoxyribonucleic acid cloning and expression of a human liver uridine diphosphate-glucuronosyltransferase glucuronidating carboxylic acid-containing drugs. J Pharmacol Exp Ther. 1993, 264: 475-479.
Gall WE, Zawada G, Mojarrabi B, Tephly TR, Green MD, Coffman BL, Mackenzie PI, Radominska-Pandya A: Differential glucuronidation of bile acids, androgens and estrogens by human UGT1A3 and 2B7. J Steroid Biochem Mol Biol. 1999, 70: 101-108. 10.1016/S0960-0760(99)00088-6.
Coffman BL, King CD, Rios GR, Tephly TR: The glucuronidation of opioids, other xenobiotics, and androgens by human UGT2B7Y268 and UGT2B7H268. Drug Metab Dispos. 1998, 26: 73-77.
Bendaly J, Fang J-L, Wiener D, Lazarus P: Functional characterization of the UGT1A9183Gly and UGT2B7268Tyr polymorphic variants. In Proceedings of the American Association for Cancer Research 95th Annual Meeting, Orlando, Florida. Abstract 2916-March 27–31, 2004
Mackenzie PI: Expression of chimeric cDNAs in cell culture defines a region of UDP glucuronosyltransferase involved in substrate selection. J Biol Chem. 1990, 265: 3432-3435.
Bhasker CR, McKinnon W, Stone A, Lo AC, Kubota T, Ishizaki T, Miners JO: Genetic polymorphism of UDP-glucuronosyltransferase 2B7 (UGT2B7) at amino acid 268: ethnic diversity of alleles and potential clinical significance. Pharmacogenetics. 2000, 10: 679-685. 10.1097/00008571-200011000-00002.
Levesque E, Beaulieu M, Green MD, Tephly TR, Belanger A, Hum DW: Isolation and characterization of UGT2B15(Y85): a UDP-glucuronosyltransferase encoded by a polymorphic gene. Pharmacogenetics. 1997, 7: 317-325.
Green MD, Oturu EM, Tephly TR: Stable expression of a human liver UDP-glucuronosyltransferase (UGT2B15) with activity toward steroid and xenobiotic substrates. Drug Metab Dispos. 1994, 22: 799-805.
Chen F, Ritter JK, Wang MG, McBride OW, Lubet RA, Owens IS: Characterization of a cloned human dihydrotestosterone/androstanediol UDP-glucuronosyltransferase and its comparison to other steroid isoforms. Biochemistry (Mosc). 1993, 32: 10648-10657.
Hernandez JS, Watson RW, Wood TC, Weinshilboum RM: Sulfation of estrone and 17 beta-estradiol in human liver. Catalysis by thermostable phenol sulfotransferase and by dehydroepiandrosterone sulfotransferase. Drug Metab Dispos. 1992, 20: 413-422.
Falany CN, Wheeler J, Oh TS, Falany JL: Steroid sulfation by expressed human cytosolic sulfotransferases. J Steroid Biochem Mol Biol. 1994, 48: 369-375. 10.1016/0960-0760(94)90077-9.
Slater CC, Hodis HN, Mack WJ, Shoupe D, Paulson RJ, Stanczyk FZ: Markedly elevated levels of estrone sulfate after long-term oral, but not transdermal, administration of estradiol in postmenopausal women. Menopause. 2001, 8: 200-203. 10.1097/00042192-200105000-00009.
Raftogianis RB, Wood TC, Otterness DM, Van Loon JA, Weinshilboum RM: Phenol sulfotransferase pharmacogenetics in humans: association of common SULT1A1 alleles with TS PST phenotype. Biochem Biophys Res Commun. 1997, 239: 298-304. 10.1006/bbrc.1997.7466.
Nowell S, Ambrosone CB, Ozawa S, MacLeod SL, Mrackova G, Williams S, Plaxco J, Kadlubar FF, Lang NP: Relationship of phenol sulfotransferase activity (SULT1A1) genotype to sulfotransferase phenotype in platelet cytosol. Pharmacogenetics. 2000, 10: 789-797. 10.1097/00008571-200012000-00004.
Zheng W, Xie D, Cerhan JR, Sellers TA, Wen W, Folsom AR: Sulfotransferase 1A1 polymorphism, endogenous estrogen exposure, well-done meat intake, and breast cancer risk. Cancer Epidemiol Biomarkers Prev. 2001, 10: 89-94.
Nandi S, Guzman RC, Yang J: Hormones and mammary carcinogenesis in mice, rats, and humans: a unifying hypothesis. Proc Natl Acad Sci USA. 1995, 92: 3650-3657.
Lopez-Otin C, Diamandis EP: Breast and prostate cancer: an analysis of common epidemiological, genetic, and biochemical features. Endocr Rev. 1998, 19: 365-396. 10.1210/er.19.4.365.
Miyoshi Y, Tanji Y, Taguchi T, Tamaki Y, Noguchi S: Association of serum estrone levels with estrogen receptor-positive breast cancer risk in postmenopausal Japanese women. Clin Cancer Res. 2003, 9: 2229-2233.
Colditz GA, Rosner BA, Chen WY, Holmes MD, Hankinson SE: Risk factors for breast cancer according to estrogen and progesterone receptor status. J Natl Cancer Inst. 2004, 96: 218-228. 10.1093/jnci/djh025.
Lower EE, Blau R, Gazder P, Stahl DL: The effect of estrogen usage on the subsequent hormone receptor status of primary breast cancer. Breast Cancer Res Treat. 1999, 58: 205-211. 10.1023/A:1006315607241.
McTiernan A, Rajan KB, Tworoger SS, Irwin M, Bernstein L, Baumgartner R, Gilliland F, Stanczyk FZ, Yasui Y, Ballard-Barabash R: Adiposity and sex hormones in postmenopausal breast cancer survivors. J Clin Oncol. 2003, 21: 1961-1966. 10.1200/JCO.2003.07.057.
Taylor CR, Shi SR, Chaiwun B, Young L, Imam SA, Cote RJ: Strategies for improving the immunohistochemical staining of various intranuclear prognostic markers in formalin-paraffin sections: androgen receptor, estrogen receptor, progesterone receptor, p53 protein, proliferating cell nuclear antigen, and Ki-67 antigen revealed by antigen retrieval techniques. Hum Pathol. 1994, 25: 263-270. 10.1016/0046-8177(94)90198-8.
McCormick D, Chong H, Hobbs C, Datta C, Hall PA: Detection of the Ki-67 antigen in fixed and wax-embedded sections with the monoclonal antibody MIB1. Histopathology. 1993, 22: 355-360.
Gerdes J, Becker MH, Key G, Cattoretti G: Immunohistological detection of tumour growth fraction (Ki-67 antigen) in formalin-fixed and routinely processed tissues. J Pathol. 1992, 168: 85-86.
Ravn V, Havsteen H, Thorpe SM: Immunohistochemical evaluation of estrogen and progesterone receptors in paraffin-embedded, formalin-fixed endometrial tissues: comparison with enzyme immunoassay and immunohistochemical analysis of frozen tissue. Mod Pathol. 1998, 11: 709-715.
Zafrani B, Aubriot MH, Mouret E, De Cremoux P, De Rycke Y, Nicolas A, Boudou E, Vincent-Salomon A, Magdelenat H, Sastre-Garau X: High sensitivity and specificity of immunohistochemistry for the detection of hormone receptors in breast carcinoma: comparison with biochemical determination in a prospective study of 793 cases. Histopathology. 2000, 37: 536-545. 10.1046/j.1365-2559.2000.01006.x.
Parl FF, Posey YF: Discrepancies of the biochemical and immunohistochemical estrogen receptor assays in breast cancer. Hum Pathol. 1988, 19: 960-966.
Andersen J, Orntoft T, Poulsen HS: Semiquantitative oestrogen receptor assay in formalin-fixed paraffin sections of human breast cancer tissue using monoclonal antibodies. Br J Cancer. 1986, 53: 691-694.
Andersen J, Poulsen HS: Immunohistochemical estrogen receptor determination in paraffin-embedded tissue. Prediction of response to hormonal treatment in advanced breast cancer. Cancer. 1989, 64: 1901-1908.
Hsu SM, Raine L, Fanger H: Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem. 1981, 29: 577-580.
Hsu SM, Soban E: Color modification of diaminobenzidine (DAB) precipitation by metallic ions and its application for double immunohistochemistry. J Histochem Cytochem. 1982, 30: 1079-1082.
Lampe JW, Bigler J, Horner NK, Potter JD: UDP-glucuronosyltransferase (UGT1A1*28 and UGT1A6*2) polymorphisms in Caucasians and Asians: relationships to serum bilirubin concentrations. Pharmacogenetics. 1999, 9: 341-349.
Lampe JW, Bigler J, Bush AC, Potter JD: Prevalence of polymorphisms in the human UDP-glucuronosyltransferase 2B family: UGT2B4(D458E), UGT2B7(H268Y), and UGT2B15(D85Y). Cancer Epidemiol Biomarkers Prev. 2000, 9: 329-333.
Carlini EJ, Raftogianis RB, Wood TC, Jin F, Zheng W, Rebbeck TR, Weinshilboum RM: Sulfation pharmacogenetics: SULT1A1 and SULT1A2 allele frequencies in Caucasian, Chinese and African-American subjects. Pharmacogenetics. 2001, 11: 57-68. 10.1097/00008571-200102000-00007.
Coughtrie MW, Gilissen RA, Shek B, Strange RC, Fryer AA, Jones PW, Bamber DE: Phenol sulphotransferase SULT1A1 polymorphism: molecular diagnosis and allele frequencies in Caucasian and African populations. Biochem J. 1999, 337: 45-49. 10.1042/0264-6021:3370045.
Nowell S, Sweeney C, Winters M, Stone A, Lang NP, Hutchins LF, Kadlubar FF, Ambrosone CB: Association between sulfotransferase 1A1 genotype and survival of breast cancer patients receiving tamoxifen therapy. J Natl Cancer Inst. 2002, 94: 1635-1640. 10.1093/jnci/94.21.1635.
Beaulieu M, Levesque E, Hum DW, Belanger A: Isolation and characterization of a novel cDNA encoding a human UDP-glucuronosyltransferase active on C19 steroids. J Biol Chem. 1996, 271: 22855-22862. 10.1074/jbc.271.37.22855.
We thank Leslie Bernstein for thoughtful review of the manuscript, and all the HEAL participants and HEAL staff for their contributions. This study was supported by SEER contract N01 PC-67009 and by the National Cancer Institute Cancer Center Support Grant NCI 5 P30 CA15704.
About this article
Cite this article
Sparks, R., Ulrich, C.M., Bigler, J. et al. UDP-glucuronosyltransferase and sulfotransferase polymorphisms, sex hormone concentrations, and tumor receptor status in breast cancer patients. Breast Cancer Res 6, R488 (2004). https://doi.org/10.1186/bcr818
- breast cancer