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Observational studies linking vitamin D deficiency with increased prostate cancer mortality and the pleiotropic anticancer effects of vitamin D in malignant prostate cell lines have initiated trials examining potential therapeutic benefits of vitamin D metabolites. There have been some successes but efforts have been hindered by risk of inducing hypercalcemia. A limited number of studies have investigated associations between variants in vitamin D pathway genes with aggressive forms of prostate cancer. Increased understanding of relevant germline genetic variation with disease outcome could aid in development of vitamin D-based therapies.
We undertook a comprehensive analysis of 48 tagging single nucleotide polymorphisms (tagSNPs) in genes encoding for vitamin D receptor (VDR), vitamin D activating enzyme 1-α-hydroxylase (CYP27B1), and deactivating enzyme 24-hydroxylase (CYP24A1) in a cohort of 1,294 Caucasian cases with an average of 8 years of follow-up. Disease recurrence/ progression and prostate cancer-specific mortality risks were estimated using adjusted Cox proportional hazards regression.
There were 139 cases with recurrence/progression events and 57 cases who died of prostate cancer. Significantly altered risks of recurrence/progression were observed in relation to genotype for two VDR tagSNPs (rs6823 and rs2071358) and two CYP24A1 tagSNPs (rs927650 and rs2762939). Three VDR tagSNPs (rs3782905, rs7299460 and rs11168314), one CYP27B1 tagSNP (rs3782130) and five CYP24A1 tagSNPs (rs3787557, rs4809960, rs2296241, rs2585428, and rs6022999) significantly altered risks of prostate cancer death.
Genetic variations in vitamin D pathway genes were found to alter both risk of recurrence/progression and prostate cancer-specific mortality.
Vitamin D has been shown to reduce cellular proliferation, increase apoptosis and inhibit invasion, migration, metastasis and angiogenesis [1–3]. The potential role of vitamin D in prostate tumor growth and aggressiveness is supported by ecological and case-control studies demonstrating an inverse relationship between prostate cancer (PCa) mortality and advanced disease with ultraviolet (UV) exposure, which is the primary source of vitamin D [4–8]. There is also an increased PCa mortality in African American and older men where skin has a reduced capacity for absorbing UV [9,10]. In early clinical trials vitamin D analogs such as calcitriol have shown some success as therapeutic agents for patients with androgen-independent PCa lesions through reduction in prostate-specific antigen (PSA) levels and increasing patient survival, however the problem of circumventing hypercalcemia has not been overcome [11,12].
Whether ingested or produced by the skin via UV exposure, vitamin D is first hydroxylated in the liver to form the metabolically inactive form of the prohormone, 25-hydroxyvitamin D [25(OH)D]. The rate limiting step is secondary conversion into the active form of the hormone, 1α,25-dihydroxy-vitamin D [1α,25(OH)2D], by 1-α-hydroxylase (1α-OHase), which is encoded by the gene CYP27B1. There is autocrine or paracrine synthesis of 1α,25(OH)2D by 1α-OHase within normal prostate cells, however expression of 1α-OHase is greatly reduced early in the neoplastic process of PCa cells [13,14]. Binding to the nuclear vitamin D receptor (VDR), which is widely expressed in prostate cells, mediates all functions of 1α,25(OH)2D. The enzyme 24-hydroxylase, encoded by the gene CYP24A1, metabolizes 1α,25(OH)2D into its excretion product calcitroic acid. Some prostate cancer cell lines have shown increased expression of the catabolic CYP24A1 in vitro .
Few genetic association studies have been conducted that specifically examined prostate cancer progression or mortality in association with vitamin D metabolism pathway genes. Some studies have attempted to address the potential association of vitamin D pathway genetic polymorphisms with prostate tumor growth and aggressiveness by examining prostate cancer risk within clinically defined subsets. For the more commonly studied polymorphisms, poly(A) microsatellite, FokI (rs10735810), BsmI (rs1544410), and TaqI (rs731236), no clear consensus has emerged from studies reporting genotype associations for men with advanced stage disease or higher Gleason scores [16–19]. Only one study has reported associations between CYP27B1 genotypes and prostate cancer risk, and no association with disease aggressiveness was noted . To better answer the question of whether germline variants within vitamin D metabolism pathway genes predict disease outcome, a study design that follows prostate cancer cases over time is a more accurate predictor of disease recurrence and survival. Three studies have looked at associations between VDR genotypes in cases who underwent radical prostatectomy and went on to exhibit recurrence, as defined by PSA failure [21–23]. For the FokI polymorphism, one study observed an increased risk of recurrence for homozygote carriers of the wildtype (G) allele, or “FF” individuals, while the other study did not corroborate the finding of an increased risk for recurrence, but did report an association with more aggressive tumors [21,22]. The third study, which looked at recurrence risk by BsmI and TaqI genotypes in Caucasians and African Americans, did not observe any association with disease outcome overall; however, they did report a significant decrease in recurrence risk for carriers of the BsmI variant (A) allele, or “B” allele, among Caucasian men with locally advanced disease .
To more carefully dissect these issues, we conducted a genetic association study of prostate cancer recurrence/progression and prostate cancer-specific mortality using a population-based cohort of men with long-term follow-up. Our study focused on three vitamin D pathway genes, VDR, CYP27B1, and CYP24A1, and used tagSNPs to better capture genetic variability within each gene. The long-term follow-up was used to access association with both recurrence/progression and mortality.
Study subjects were enrolled in one of two population-based prostate cancer case-control studies that have been described previously [24,25]. Cases were newly diagnosed with histologically confirmed prostate cancer in two study periods, either January 1, 1993 to December 31, 1996 (Study I, age range 40–64 years) or January 1, 2002 to December 31, 2005 (Study II, age range 35–74 years). Prostate cancer cases were identified from the metropolitan Seattle-Puget Sound population-based tumor registry that part of the National Cancer Institute’s Surveillance, Epidemiology, and End Results (SEER) program. Of the 1,754 eligible, interviewed cases we obtained peripheral blood leukocyte samples for genotyping from 1,458 men. From this group we excluded 16 cases because they did not have sufficient DNA for this specific study and further limited this dataset to Caucasians for a total of 1,294 cases (Study I: n=585; Study II: n=709).
The recurrence/progression analysis was limited to a subset of 458 cases in Study I; subjects were excluded if they were alive but did not fill out a follow-up questionnaire or give access to medical record review (n=109) or had an initial diagnosis of metastatic disease (n=18). In January 2004 a self-administered follow-up questionnaire collecting information on use of secondary therapies, follow-up PSA results, and evidence for prostate cancer recurrence/ progression was sent to Study I cases. The overall response level was 82% and showed no association between clinical parameters and non-response . Data from this survey was used to determine recurrence/progression status for 426 cases. An additional 32 cases who were diagnosed with local/regional disease and who were deceased at the time of the follow-up survey had recurrence/progression data available; 21 of these cases had next-of-kin provided consent for medical record review, which was used to determine recurrence/progression status, and 11 of these cases died of metastatic prostate cancer and were coded as having recurred. The survival analysis included all 1,294 cases from both studies. The SEER registry provided information on tumor characteristics, primary therapy, vital status, and underlying cause of death. Death certificates were obtained to confirm fatal prostate cancer. The agreement between the SEER registry and death certificate has been reported to be excellent . The most recent registry linkage update for mortality was June 15, 2009. This study was approved by Fred Hutchinson Cancer Research Center’s Institutional Review Board, all subjects had informed consent, and genotyping was approved by the Internal Review Board of the National Human Genome Research Institute.
SNPs that captured the genetic variability in the VDR  and CY27B1  genes were selected using resequencing data, while SNP selection for CYP24A1  used publicly available from HapMap consortium data (www.hapmap.org). Using parameters of r2 ≥ 0.8 and minor allele frequency ≥ 5% , a total of 25 tagSNPs for VDR (chromosome 12q13, length 63.4 kb, 9 exons), 3 tagSNPs for CYP27B1 (chromosome 12q13, length 4.8 kb, 9 exons), and 20 tagSNPs for CYP24A1 (chromosome 20q13; length 20.5 kb, 12 exons) were chosen.
The Applied Biosystems (ABI) SNPlex™ Genotyping System was used for genotyping, and proprietary GeneMapper® software (www.appliedbiosystems.com) was used for calling alleles. Discrimination of specific SNP alleles was determined by an ABI 3730xl DNA Analyzer and is based on presence of a unique sequence assigned to the original allele-specific oligonucleotide. The SNPlex assay could not be designed for 7 tagSNPs and 3 tagSNPs failed genotyping after the design stage; accordingly, we present results for 22 tagSNPs for VDR, 2 tagSNPs for CYP27B1, and 14 tagSNPs for CYP24A1. Quality control included genotyping of 76 blind duplicate samples, which revealed 99% agreement on genotyping calls across all SNPs assayed. In addition, each batch of DNA aliquots genotyped incorporated similar numbers of case and control samples, and laboratory personnel were blinded to case-control status of samples. The call rate was ≥97% for all but two SNPs (VDR rs2238139, 96%; CYP24A1 rs6127118, 95%). Further details of genotyping methods are described elsewhere . All SNPs included in this study were consistent (p > 0.05) with Hardy-Weinberg equilibrium (HWE) with the exception of CYP24A1 rs13038432 (p < 0.001).
For each SNP we classified homozygote carriers of the common allele as the referent group and carriers of the less common variant allele as the exposure group. We used both dominant and co-dominant models, except when no individuals were homozygous for the variant genotype. Trend tests, which used a single indicator variable coded as the number of variant alleles for each SNP, were used to assess gene dosage. To examine associations between individual SNPs with prostate cancer recurrence/progression and prostate cancer-specific mortality we used Cox proportional hazards (PH) regression models adjusting for age, Gleason score [2–6, 7(3+4), or 7(4+3)-10], stage at diagnosis (local, regional, or distant), diagnostic PSA level (0–9.9 or ≥10.0 ng/mL), and primary treatment [radical prostatectomy, radiation with or without androgen deprivation therapy (ADT), ADT only, other treatment, or active surveillance]. Analysis was also done limiting dataset to men treated with radical prostatectomy.
Time to prostate cancer recurrence/progression was defined as time from diagnosis to the first reported evidence of recurrence as described previously . For those with follow-up but without an event, the censoring date was the date that the follow-up questionnaire was returned. For the 11 cases who were diagnosed with localized/regional disease but died of prostate cancer prior to follow-up survey administration, time to recurrence was imputed . Time to prostate cancer-specific mortality was defined as the time from diagnosis to death. Living cases were censored on date of most recent linkage with the cancer registry. Cases that died from other or unknown causes were censored at the time of death.
Gene-environment interactions were assessed for first-degree family history of prostate cancer, body mass index (BMI), and vitamin D supplement use/dietary intake for both disease recurrence/progression and survival in Cox PH regression models with and without interaction terms. Models were compared using the likelihood ratio test. Vitamin D intake was calculated using food frequency and supplement use questionnaires administered separately from the original interview for 1,305 of the 1,442 cases. For the interaction analyses, PH models were limited to risk estimates assuming a dominant genetic model, combining heterozygotes and homozygous variants as the exposed group.
To account for the effect of multiple testing, sets of outcomes (PCa mortality or recurrence/progression) and clinical covariates were permuted in order to approximate distribution of covariate adjusted p-values under the null hypothesis. For each permutation, dominant, codominant and trend models were fit for all SNPs and the minimum p-values kept for each SNP. P-values were ordered to approximate null distribution of the order statistics, i.e., minimum p-value, second smallest p-value, etc. The original p-values were also ordered and permutation p-values were calculated by comparing the ordered p-values to the null distribution for the appropriate order statistic. Permutation p-values can be interpreted as the probability of observing a p-value less than or equal to what was observed for the given order statistic under the null hypothesis of no association with disease outcomes for any of the 38 SNPs. A SNP was considered to be significantly associated with prostate cancer mortality or recurrence/progression if the nominal p-value and the permuted p-value were both less than 0.05.
A stepwise AIC (Akaike’s Information Criterion) regression procedure was used to develop predictive models for prostate cancer mortality and recurrence/progression. The procedure was restricted to include all clinical predictors in the final model (age, stage, Gleason score, diagnostic PSA and primary treatment). Empirical ROC (receiver operating characteristic) curves for 5- and 10-year prostate cancer mortality and recurrence/progression were used to compare the prognostic accuracy of models containing SNPs and clinical covariates versus baseline models with only clinical covariates. Improvement of prediction accuracy due to addition of optimal SNPs selected by the AIC stepwise regression approach was summarized by comparing ROC (.2), sensitivity at a specificity of 80%, and area under the ROC curve (AUC). Bootstrap confidence intervals were presented for differences in ROC (.2) and AUC. All analyses were done using R version 2.8.1 and the STATA statistical package (version 10.1, STATA Corp., College Station, TX).
There were 139 events of recurrence/progression, with an average 8.2 years of follow-up (range 0.1–12.8 years) after diagnosis. For cases having recurrence/progression events, a greater proportion were diagnosed at younger ages, with regional stage of disease (cases with distant stage were excluded), higher Gleason scores, and diagnostic PSA values greater than 10 ng/mL (Table 1). There were 57 cases who died of prostate cancer in the average 8.5 years of follow-up (range 0.8–15.9 years). For cases who died of prostate cancer, a greater proportion were at diagnosed at younger ages, with regional or distant stages of disease, higher Gleason scores, diagnostic PSA values greater than 10 ng/mL, and a BMI greater than or equal to 30 kg/m2 (Table 1).
Two VDR tagSNPs (rs6823 and rs2071358) and one CYP24A1 tagSNP (rs2762939) showed increased risks of disease recurrence/progression for carriers of the less common alleles (Table 2). When cases were limited to men treated with radical prostatectomy, the increased risks were still significant for carriers of less common alleles for VDR rs6823 [HR 2.0 (95% CI 1.2–3.3)] and CYP24A1 rs2762939 [HR 1.3 (95% CI 1.0–2.4)], but not VDR rs2071358. One CYP24A1 tagSNP (rs927650) showed decreased risk of disease recurrence/progression for carriers of the less common allele, but this decreased risk estimate was not apparent when cases were limited to those treated with radical prostatectomy (Table 2). Only CYP24A1 rs2762939 retained significance in a logistic model unadjusted for clinical parameters. None of the tagSNPs retained significance after adjustment for multiple comparisons. There was no evidence of interaction with self-report of family history of prostate cancer, BMI, or vitamin D supplement use/dietary intake.
Two VDR tagSNPs (rs3782905 and rs11168314) and two CYP24A1 tagSNPs (rs2585428 and rs6022999) showed increased risks of prostate cancer-specific mortality for carriers of the less common alleles (Table 2). One VDR tagSNP (rs7299460), one CYP27B1 tagSNP (rs3782130) and three CYP24A1 tagSNPs (rs3787557, rs4809960, and rs2296241) showed decreased risks of prostate cancer-specific mortality (Table 2). When cases were limited to men treated with radical prostatectomy, risks of prostate cancer-specific mortality did not remain significant for carriers of the less common alleles for any of the SNPs. Only VDR rs11168314 retained significance in a logistic model unadjusted for clinical parameters. None of these tagSNPs remained significant after adjustment for multiple comparisons. There was no evidence of interaction with self-report of family history of prostate cancer or vitamin D supplement use/dietary intake. For BMI there was a suggestion of effect modification for three CYP24A1 tagSNPs, rs3787557 (p < 0.01), rs4809960 (p < 0.001), and rs2296241 (p = 0.05), but the sample size was too small to reliably report hazard ratios for each BMI strata.
The ROC curves in figure 1 illustrate the prognostic value of clinical parameters alone versus these same parameters plus a panel of the 7 “optimal” SNPs (VDR: rs731236, rs3782905, rs2408876, rs7299460 and rs6823; CYP24A1: rs927650 and rs2762939) for predicting recurrence/progression at 5 years after diagnosis. The sensitivity for 5-year recurrence/ progression at a specificity of 80% was 53.7% for the model using only the clinical predictors, however, the sensitivity increased to 75.6% when the 7 SNP panel was added (difference: 21.9, 95% CI: 0.0%, 40.9%, p = 0.044). The difference in the AUC between the two curves was 0.082 (95% CI 0.016, 0.180, p = 0.020). The ROC curves in figure 2 illustrate the prognostic value of clinical parameters alone versus these same parameters and a panel of 6 “optimal” SNPs (VDR: rs2544038, rs731236, rs3782905, rs7299460; CYP27B1: rs3782130; CYP24A1: rs6022999) for predicting prostate cancer-specific mortality at 10 years after diagnosis. At 80% specificity, the sensitivity for 10-year prostate cancer-specific mortality was 91.4% using only the clinical predictors and increased to 94.3% when the 6 SNPs were included (difference: 2.9, 95% CI: −4.0%, 15.5%, p = 0.2). The difference in AUC between the two ROC curves was 0.018 (95% CI 0.005, 0.050, p = 0.128).
We found some significant associations between risk of both tumor recurrence/progression and prostate cancer death for several SNPs in the VDR, CYP27A1 and CYP24A1 genes, however, associations at for individual SNPs did not remain significant after adjustment for multiple comparisons. Comparison of ROC curves suggests that addition of an optimal panel of SNPs to existing clinical predictors may improve predictive models for prostate cancer recurrence/ progression. Addition of the 7 SNP panel (VDR: rs731236, rs3782905, rs2408876, rs7299460 and rs6823; CYP24A1: rs927650 and rs2762939) significantly improved sensitivity at a specificity of 80% and AUC for a predictive model of 5-year prostate cancer recurrence/progression. Our previous work has not supported a consistent association between genetic variation in VDR, CYP27B1, and CYP24A1 genes and prostate cancer risk [32,33]. However, since vitamin D may play a different role in disease initiation versus disease progression, polymorphisms that predict disease outcomes are likely to be different than those that predict disease risk. Research has consistently shown a link between vitamin D and prostate cancer progression specifically; cellular studies show vitamin D can inhibit the carcinogenic progression of prostate cells, while ecologic studies provide evidence that UV exposure affects survival and prognosis [1–8].
Several VDR SNPs were identified to be associated with recurrence/progression, either by individual genotype before adjustment for multiple comparisons (rs6823 and rs2071358) or by the AIC approach for the ROC analysis (rs731236, rs3782905, rs2408876, rs7299460 and rs6823). Likewise, several VDR SNPs were shown to be associated with prostate cancer death, either at an individual level before adjustment for multiple comparisons (rs3782905, rs11168314, and rs7299460) or by the AIC approach for the ROC analysis (rs2544038, rs731236, rs3782905, and rs7299460). All of these SNPs, with the exception of rs731236, a synonymous coding SNP also known as the TaqI polymorphism (conservation score 0.175), are intronic, are not found to be evolutionarily conserved (conservation score < 0.001), and their potential biological consequences are unknown. Three of these SNPs, rs731236, rs3782905, and rs7299460 are included in both ROC models for recurrence/prediction and mortality. The TaqI polymorphism, rs731236, is not functional but is in linkage disequilibrium (LD) with a poly(A) microsatellite repeat in the 3’ untranslated region (UTR) that is thought to be important in post-transcriptional control gene expression. The SNP rs3782905 is in the DNA binding domain responsible for interaction with vitamin D response elements (VDRE) in target genes. The SNPs rs2408876, rs7299460, rs11168314, rs6828 and rs2071358 are located in either the promoter region or 5’ UTR and could be in LD with several recently reported novel SNPs that have both high conservation and apparent functional consequence affecting VDR transcription [34–37]. The SNP rs11168314 is in LD (r2 = 0.82) with Cdx-2 (rs11568820) that has been shown to alter transcription .
Polymorphisms in the genes involved in 1α,25(OH)2D metabolism were also found to be associated with both tumor recurrence/progression or prostate cancer-specific mortality. The one polymorphism in CYP27B1, rs3782130, associated with prostate cancer death, was not found to be evolutionarily conserved, but is located in the 3’ UTR. To date, there is limited evidence identifying functional polymorphisms in CYP27B1. It is interesting to note that CYP27B1 is down-regulated early in the neoplastic process of prostate cancer cells by epigenetic regulation, thus germline genetic variation affecting either gene expression or protein function may not have as large an effect within the malignant cell milieu [13,14,38]. The seven CYP24A1 SNPs that were associated with either tumor recurrence/progression (rs927650 and rs2762939) or prostate cancer-specific mortality (rs3787557, rs4809960, rs2296241, rs2585428, and rs6022999) were intronic and were not evolutionarily conserved with the exception of rs2296241 (conservation score 0.99), a synonymous polymorphism in exon 4. CYP24A1 was the only gene for which we used publicly available data as compared to resequencing data; consequently we are limited by the publically available genetic variants. The functional effects of indentified SNPs remain unclear but several novel SNPs have been recently identified in the promoter region 5' of exon 1 in CYP24A1 that have demonstrated a functional impact on VDRE binding and transactivation in vitro and altered expression of CYP24A1 gene expression in vivo . The SNPs near this region, rs4809960, rs2296241, rs2585428, and rs6022999, could potentially be in LD with the true functional SNPs.
There were no SNPs found to be associated with both recurrence/progression and prostate cancer-specific mortality at the individual genotype level although there were three VDR SNPs, rs7311236, rs3782905, and rs7299460, that were included in both ROC models. The lack of corresponding associations with both outcomes for a given genotype does not necessarily diminish the potential association with individual outcomes because the outcome measures are not synonymous. Only 20% (n=28) of the 139 cases with recurrence/progression events also died of prostate cancer. This is mostly likely because patients who had an initial diagnosis of metastatic disease were excluded from recurrence/progression analysis. It could also be due to the fact that almost half (n=66) of the events were based on evidence of biochemical recurrence alone which is not predicative of PCa-specific mortality since the natural history of biochemical recurrence is so heterogeneous .
Excess body weight, measured by BMI, may be associated with increased risk of prostate cancer progression, higher risk of biochemical failure after treatment of disease, and an increased risk of dying from the disease [41,42]. Increased BMI is also associated with decreased levels of bioavailable 25(OH)D . While the apparent association between adiposity and poorer prognosis is complex and multi-factorial, is has been suggested that vitamin D levels may play a role thus BMI could potentially modify the effect of these genotypes. There have been reported interactions between VDR polymorphisms and adiposity with risk of colon cancer . Our findings were not appreciably different when we controlled for BMI, however we did find a suggestion of effect modification for CYP24A1 rs3787557 (p < 0.01), rs4809960 (p < 0.001), and rs2296241 (p = 0.05) with BMI for risk of recurrence/progression.
While we were able to account for dietary intake of vitamin D, we were not able to measure serum levels of 25(OH)D or UV light exposure, the primary source of vitamin D. Studies examining serum vitamin D levels with risk of PCa overall have had inconsistent results and do not seem suggest an association between levels 25(OH)D or 1α,25(OH)2D in the blood with risk of the disease [19,29,30,45,46]. This could be because measured serum levels may not correspond to vitamin D exposure during the long latency period of prostate cancer or reflect the prostate tissue-specific levels since local synthesis of 1α,25(OH)2D is independent of the tight regulation in the endocrine system . Despite the lack of evidence for an association between Vitamin D levels in the blood and prostate cancer risk, there is evidence that vitamin D could be a potential effect modifier of disease risk within VDR genotypes [6,7,45,46,48]. It may be worthwhile for future studies to quantify vitamin D level in cases not only because of this potential interaction, but because serum levels of 1α,25(OH)2D may have a larger impact of cancer progression as a consequence of the down-regulation of CYP27A1 in the malignant prostate cells. A study that examined relationship between vitamin D status and survival rather than disease risk supports this hypothesis; a deceased risk of prostate cancer-specific mortality was observed in subjects with medium to high levels of 25(OH)D in serum collected upon admission to hospital for treatment .
This was a unique analysis with respect to vitamin D-related genes and prostate cancer prognosis in that it included long-term follow-up of all cases in a population-based study. Inclusion of tagSNPs to better capture genetic variation in each gene within this pathway allowed for a more comprehensive analysis than past studies. We were able to include relevant demographics and treatment variables to find a SNP panel that was predictive of outcome beyond clinical parameters currently used by clinicians. Although there was treatment heterogeneity among our cases, we were able to limit analyses to men receiving radical prostatectomy and replicate some of our findings. The primary weakness of our study was sample size, thus we must recognize the lack of precision in these findings and underscores the need for replication especially with respect to the ROC curves. Sample size also limited our analysis with respect to potential effect modifiers such as BMI. We did not include a stratified analysis by race because there were only 10 recurrence/progression events and nine prostate cancer deaths within African Americans in our dataset. Future studies should examine risk within African Americans since it has been postulated that the higher fraction of vitamin D deficiency observed in African American men may contribute to the increased mortality of prostate cancer observed in this population [10,50].
By studying a group of SNPs that more fully captured the genetic variability in the VDR, CYP27B1, and CYP24A1 genes, we found some evidence that genetic variation in these genes may be associated with both disease recurrence/progression and prostate cancer death and lead to an improved risk prediction. These findings should lead to future replication studies of germline genetic polymorphisms that can be used for risk prediction and to improve prostate cancer patient outcomes. These studies should include greater coverage of the promoter regions, especially for CYP24A1, in addition to examining coactivators and corepressers that modulate the response of VDR antiproliferative effects on prostate cells.
FINANCIAL SUPPORT: This work was supported by grants RO1-CA56678, RO1-CA092579, RO1-CA082554 and P50-CA097186 from the National Cancer Institute; additional support was provided by the Fred Hutchinson Cancer Research Center, the Intramural Program of the National Human Genome Research Institute, and the Prostate Cancer Foundation Young Investigator Award Grant.
The authors of this manuscript do not have any affiliations that are relevant or important with any organization that to our knowledge has a direct interest, financial or otherwise, in the subject matter discussed.