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# An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk

## Abstract

It remains elusive whether some of the associations identified in genome-wide association studies of prostate cancer (PrCa) may be due to regulatory effects of genetic variants on CpG sites, which may further influence expression of PrCa target genes. To search for CpG sites associated with PrCa risk, here we establish genetic models to predict methylation (N = 1,595) and conduct association analyses with PrCa risk (79,194 cases and 61,112 controls). We identify 759 CpG sites showing an association, including 15 located at novel loci. Among those 759 CpG sites, methylation of 42 is associated with expression of 28 adjacent genes. Among 22 genes, 18 show an association with PrCa risk. Overall, 25 CpG sites show consistent association directions for the methylation-gene expression-PrCa pathway. We identify DNA methylation biomarkers associated with PrCa, and our findings suggest that specific CpG sites may influence PrCa via regulating expression of candidate PrCa target genes.

## Introduction

Prostate cancer (PrCa) is the second most frequently diagnosed malignancy among men and the fifth leading cause of cancer death worldwide1. Its survival rate is relatively high for localized stage disease, but decreases substantially for metastatic disease2. Effective strategies are critical for risk assessment, screening, and early detection of PrCa, aimed at decreasing its public health burden. Although prostate-specific antigen (PSA) has demonstrated efficacy for detecting PrCa early3,4, there lacks a clear cutoff point for PSA with high sensitivity and specificity5,6,7. The benefits of PSA screening for reducing PrCa mortality remains controversial8,9,10. Furthermore, there are adverse effects, such as overdiagnosis11. Therefore, additional effective biomarkers are needed for risk assessment and early detection of PrCa.

Aligned with findings of a crucial role for DNA methylation in PrCa development12, research has identified several methylation markers to be potentially associated with PrCa risk, such as methylation at GSTP1, CDKN2A, DNMT3B, SCGB3A1, and HIF3A12,13,14,15,16. However, most prior studies have assessed only a couple of candidates. Recent emerging studies profiling genome-wide methylation usually included a relatively small number of subjects17, resulting in inadequate power for the identification of associated methylation biomarkers. Besides these limitations, there are a number of biases commonly encountered in conventional epidemiologic studies, including selection bias, uncontrolled confounding, and reverse causation, that make it difficult to determine whether the identified associated markers are causally associated with PrCa.

One strategy to reduce some of these biases is to use genetic variants to develop an instrument to assess the association between DNA methylation and PrCa. Such an approach is based on the principle of the random assortment of alleles from parents to offspring during gamete formation, and thus a genetically determined proportion of DNA methylation levels should be less susceptible to selection bias and reverse causation in principal. Research has shown that a large portion of CpG sites have high heritability18,19. Genome-wide association studies (GWAS) have also identified a large number of genetic loci associated with DNA methylation levels20,21. Many of these genetic variants could potentially serve as strong instrumental variables for evaluating associations between DNA methylation and PrCa risk in an adequately powered study.

Besides a potential utility in improving PrCa risk assessment, the identification of promising DNA methylation markers using a design of genetic instruments may also contribute to understanding of the genetics and etiology of PrCa. Epidemiological research provides strong support for a genetic predisposition to PrCa22,23. To date, GWAS have identified ~150 genetic loci for PrCa24,25,26. However, together these variants explain <30% of the familial relative risk, and the underlying biological mechanisms for a majority of the identified loci remain unclear24. Recently, we performed a large transcriptome-wide association study (TWAS) of PrCa, in which we identified multiple associations between genetically predicted gene expression and PrCa risk27. Interestingly, many of the associated genes were identified to be candidate target genes of GWAS-identified risk SNPs27. Aligned with the recognized role of DNA methylation in regulating gene expression, we hypothesize that some GWAS-identified risk SNPs may regulate expression of their target genes through influencing DNA methylation levels. In this study, we perform a large integrative multi-omics analysis involving data of genomics, methylomics, and transcriptomics aiming to uncover novel CpG sites and genes that may contribute to PrCa development.

## Results

### DNA methylation prediction models

Using FHS data, we were able to build DNA methylation prediction models for 223,959 CpG sites, of which 81,432 showed a prediction performance (R2) of at least 0.01 (≥10% correlation between predicted and measured DNA methylation levels). For 77,243 of those CpG sites, there were no SNPs within the binding site. Interestingly, there tended to be positive weak correlations between methylation prediction model performance and number of input variants within the 2-MB window of each CpG site (Pearson correlation coefficient 0.03, P = 1.60 × 10−13; Spearman correlation coefficient 0.02, P = 1.43 × 10−6). We further applied these 77,243 models to the genetic data in WHI and evaluated their performance by comparing predicted methylation levels with measured levels. Overall, DNA methylation that could be predicted well in FHS also tended to be predicted well in WHI (a correlation coefficient of 0.96 for R2 in two datasets; Supplementary Fig. 1). These 77,243 CpG sites were selected for analyses for their associations between predicted DNA methylation and PrCa risk.

### Associations of genetically predicted methylation with PrCa

Of the 77,243 CpG sites tested, genetically predicted DNA methylation of 759 located at 82 genomic loci were associated with PrCa risk after Bonferroni correction (P ≤ 6.47 × 10−7) (Table 1; Supplementary Table 1 and Supplementary Data 1; Manhattan plot in Fig. 1). This included 15 located at 10 genomic loci that were more than 500 kb away from any PrCa risk variant identified in GWAS or fine-mapping studies (Table 1). An association between a higher DNA methylation level and increased PrCa risk was detected for cg18800143, cg07645299, cg12627844, cg16397176, cg11562153, cg13866093, cg00444740, cg20100049, cg22370235, cg04739953, cg01715842, and cg23397578. Conversely, an inverse association between methylation level and PrCa risk was identified for cg24388424, cg06836406, and cg13230424. Of these 15 CpG sites at novel loci, after conditioning on the near PrCa risk variant, the associations of genetically predicted DNA methylation levels for four CpG sites (cg18800143, cg16397176, cg06836406, and cg13230424) remained at P ≤ 6.47 × 10−7 (Table 1).

For the remaining 744 CpG sites located at known PrCa risk loci (Supplementary Table 1 and Supplementary Data 1), after conditioning on the adjacent PrCa risk SNP, an association at P ≤ 6.47 × 10−7 persisted for 63 CpG sites (Supplementary Table 1). This suggests that the associations of these 63 CpG sites with PrCa risk are potentially independent of the PrCa risk SNPs identified in GWAS or fine-mapping studies (Supplementary Table 1). For the other 681 CpG sites, their associations with PrCa risk became weaker, if not completely attenuated, after conditioning on the PrCa risk SNP (Supplementary Data 1). These are potentially due to (1) the previously identified associations of risk SNPs with PrCa at these loci may be mediated through the DNA methylation of these CpG sites identified in the current study, or (2) confounding effects (Supplementary Data 1). We estimated that the 15 CpG sites at novel loci and the 63 CpG sites independent of PrCa risk SNPs could explain 0.69% of familiar risk of PrCa (methods in Supplementary Information).

Based on annotation using ANNOVAR, there were substantial inflations of the “exonic” and “ncRNA exonic” regions for the identified PrCa-associated CpG sites when compared with the overall tested 77,243 CpG sites (chi-square tests: 15.28% versus 7.44%, P = 6.36 × 10−16; 5.53% versus 2.42%, P = 6.37 × 10−8) (Supplementary Table 2). Also, a substantial decreased proportion of the “intergenic” region was observed (chi-square test: 15.42% versus 25.10%, P = 1.13 × 10−9) (Supplementary Table 2).

Through an annotation of the 759 PrCa-associated CpG sites using eFORGE v1.2, there tends to be an overlap of their positions with regions containing lysine 4 mono-methylated H3 histone (H3K4me1) markers across 38 of 39 cell types included in the consolidated Roadmap Epigenomics Project, including blood tissues (Supplementary Fig. 2). This suggests that the identified CpG sites associated with PrCa risk may be enriched in enhancers and may be involved in transcriptional activation. We also observed significant enrichment for the associated CpG sites with positions of genes encoding transcription factors (P = 0.001).

For the identified 759 CpG sites showing an association in the PRACTICAL, CRUK, CAPS, BPC3, and PEGASUS consortia, we further evaluated their associations using independent UK Biobank data. In this analysis with far fewer PrCa cases, 554 CpG sites (73%) also showed an association at P < 0.05 with the same direction of effect (Supplementary Data 2). These suggested that the CpG-PrCa risk associations identified in the main analyses using data of the PRACTICAL, CRUK, CAPS, BPC3, and PEGASUS consortia were quite robust. We performed downstream analyses focusing on these 759 CpG sites.

### Potential target genes of the PrCa-associated CpG sites

Of the 759 PrCa-associated CpG sites, association analyses were performed for 689 pairs of CpG site-gene, including 613 CpG sites with 244 flanking genes. Overall, associations at a false discovery rate (FDR) < 0.05 were observed for methylation levels of 42 CpG sites with expression of 28 neighbor genes in blood tissue (Supplementary Table 3). Interestingly, we also observed several associations between DNA methylation and expression of genes encoding transcription factors at P < 0.05 (Supplementary Table 4). In the TCGA dataset of tumor-adjacent normal prostate tissue, albeit with a quite limited sample size (n = 34), we observed that 26 of the 37 associations that could be assessed showed the same direction of effect compared with that in the blood tissue (Supplementary Table 5). Among them, 11 showed statistical significance at P < 0.05 in this small dataset (Supplementary Table 5).

### Associations of potential target genes with PrCa risk

Of the 28 potential target genes of the identified CpG sites based on blood tissue analyses, blood tissue gene expression prediction models were built for 22 genes, and prostate tissue prediction models were built for 14 genes with a prediction performance (R2) of at least 0.01 (≥10% correlation). Using the S-PrediXcan method, we evaluated associations between the genetically predicted expression of these genes and PrCa risk. Of the 22 genes with blood tissue prediction models built, 18 demonstrated an association at FDR < 0.05 (Table 2). For 12 of them with prostate tissue prediction models built as well, nine showed an association at P < 0.05 (Table 2). For all of the nine genes except for VPS53, the direction of associations was consistent for the predicted expression in blood versus prostate tissue. Of two other genes with models built for prostate tissue only, HLA-DOB showed a significant association with PrCa risk (beta = 0.068, P = 2.65 × 10−4), and C11orf21 did not show a significant association (P = 0.21).

### Associations showing consistent direction of effect

There were 25 CpG sites and 14 genes with consistent directions of association for the DNA methylation–gene expression–PrCa pathway (Table 3). For example, the CpG site cg20240347 located upstream of MDM4, and its DNA methylation level was positively associated with expression of MDM4 (coefficient 0.21; P = 1.69 × 10−14). There was an inverse association between genetically predicted expression of MDM4 and PrCa risk (OR = 0.36; P = 1.55 × 10−19). There was also evidence supporting the genetically predicted DNA methylation of cg20240347 to be associated with a decreased PrCa risk (OR = 0.93; P = 2.61 × 10−19). Interestingly, MDM4 has been previously implicated as a potential target gene that is responsible for the identified association signal of index SNP rs4245739 in GWAS25, and in our recent TWAS study27. Our results highlight a possible role of the CpG site cg20240347 in the underlying biological mechanism of the link between MDM4 and PrCa. Whether the DNA methylation of these CpG sites at the corresponding loci of the genes in Table 3 may play a role in PrCa etiology through the regulation of expression of these genes warrants further investigation. Ingenuity pathway analysis (IPA)28 suggested potential enrichment of cancer-related functions for the 14 implicated genes (Supplementary Table 6). The top canonical pathways identified included cell cycle (P = 0.033) and cancer drug resistance (P = 0.039). It is worth noting that based on the predicted DNA methylation–PrCa risk, DNA methylation–gene expression, and predicted gene expression–PrCa risk results, we also observed six CpG sites and four genes (VAMP8, C4B, BAIAP2L1, and NCOA4) with inconsistent directions of association for the DNA methylation–gene expression–PrCa pathway (Supplementary Table 7). Of these genes, NCOA4, BAIAP2L1, and VAMP8 are candidate PrCa susceptibility genes identified in earlier TWAS27,29,30. Future work is needed to better understand these associations.

## Discussion

This is the first large-scale study to comprehensively evaluate associations of genetically predicted DNA methylation levels with PrCa risk. We identified 759 CpG sites whose predicted DNA methylation levels demonstrated an association after Bonferroni correction, including 15 located at novel loci. Of the 744 CpG sites located at known PrCa risk loci, 63 showed an association, even after conditioning on adjacent PrCa risk SNPs. In additional analyses involving gene expression, we observed some evidence suggesting that 25 CpG sites may influence PrCa risk via regulating expression of 14 candidate PrCa target genes. Our study provided substantial information to improve the understanding of genetics and etiology for PrCa, and it also generated multiple CpG sites as potential biomarkers for risk assessment of PrCa, the most common male malignancy globally.

For processing DNA methylation data for genetic model building, we performed quartile normalization for subjects followed by rank normalization for methylation levels, a standard approach widely used in the community for DNA methylation analyses31. We acknowledge, however, that such an approach could be suboptimal for CpG sites whose distributions of methylation do not resemble standard normal. Future endeavors for developing more sophisticated methods to deal with this are needed to pick up additional relevant signals. In this study, we identified 759 associated CpG sites, of which 42 were observed to be associated with expression of 28 flanking genes that were annotated by ANNOVAR, based on positions. For the other identified CpG sites, it is possible that genes that are not the most proximal ones could be target genes for local or distal regulation. However, to determine the exact target genes of these CpG sites involves additional lines of evidence besides statistical association, which is beyond the scope of this study. We observed 25 CpG sites with consistent directions of association for the DNA methylation–gene expression–PrCa pathway. Of the 14 linked genes, 10 (MDM4, NUCKS1, PM20D1, VAMP5, GPR160, PDK1, UHRF1BP1, MCAT, LY6G5C, and VPS53) demonstrated an association with PrCa risk in recent TWAS studies27,30. Furthermore, MDM4 and NUCKS1 have been previously implicated as potential target genes at GWAS-identified PrCa risk loci25,32. Our results incorporating DNA methylation provide additional insight into the potential mechanism for the link between these genes and PrCa development. Interestingly, in vitro experiments of silencing PDK1 could decrease cell proliferation and inhibit the invasion and migration capability of PrCa cells33. Further functional studies are needed to better characterize whether there are potential regulatory effects of the identified 25 CpG sites on the expression of the 14 adjacent genes for PrCa development. Importantly, our design of integrating genome, methylome, and transcriptome data provides some evidence that 25 CpG sites may regulate expression of 14 candidate target genes, which further influences PrCa risk. Through the innovative integrative analyses harnessing large-scale human subject data, our study not only identifies several associations consistent with prior findings but it also uncovers potentially important roles of novel CpG sites and putative target genes (e.g., CFAP44, TRIM26, MICB, and ZDHHC7) in prostate tumorigenesis.

For the aim of identifying effective methylation biomarkers for risk assessment of PrCa, a design focusing on blood tissue would be optimal. Such a design could be suboptimal for characterizing the biological mechanism of PrCa development, when compared with the design using genetic instruments of DNA methylation levels identified in prostate tissue, considering potential tissue specificity in DNA methylation levels. On the other hand, research has shown that the genetic regulation of DNA methylation for many CpG sites tends to have a cross-tissue consistency, as indicated by studies comparing blood and different brain region tissues, and among lung, breast, and kidney tissues20,34. Furthermore, it is challenging to obtain prostate tissues from a large number of healthy individuals. Although prostate tumor-adjacent normal tissue methylation data are available in TCGA, tumor-adjacent normal tissue samples from PrCa patients may contain cancer cells; therefore, the methylation profile of these samples could be different from that of normal prostate tissue samples from healthy men. The statistical power for the model building using TCGA data could also be low due to the relatively small sample size available. In this study, for assessing DNA methylation–gene expression associations to determine potential target genes of identified CpG sites, besides using data from blood tissue (Supplementary Table 3), we also leveraged data from tumor-adjacent normal prostate tissue in TCGA. Despite a small sample size, we observed evidence supporting many of the associations identified using blood tissue data (Supplementary Table 5). For evaluating predicted gene expression–PrCa risk associations, our analyses using prostate tissue gene expression prediction models also support many of the associations identified using blood tissue prediction models (Table 2).

In the current work, a large number of subjects (N = 1595) in the reference FHS dataset was used for the DNA methylation prediction model building. Aligned with the huge sample size for our main association analyses for PrCa risk (79,194 cases and 61,112 controls), our study provides an unparalleled opportunity to detect the DNA methylation–PrCa associations. The use of genetic instruments rendered our study as potentially less susceptible to several limitations commonly encountered in conventional epidemiological studies, such as selection bias and reverse causation. On the other hand, it is worth noting that similar to TWAS, the associations observed in our analyses focusing on CpG sites are also vulnerable to confounding due to pleiotropy and co-localization of genetic signals. For instance, it would be difficult to distinguish a situation in which one causal methylation quantitative trait locus (mQTL) regulates the methylation of two CpG sites from a scenario in which two CpG sites have two causal mQTLs that are in linkage disequilibrium (LD) with each other. Correlated total methylation levels across CpG sites, correlated predicted DNA methylation across CpG sites, as well as shared genetic variants between DNA methylation genetic prediction models and gene expression prediction models, could all lead to spurious associations in our analyses35. When faced with two correlated predictors, regularized regression models like elastic net will randomly down weight one of them, which may be the true causal variant. Despite these potential limitations, our study generated a list of promising PrCa-associated CpG sites that warrant further investigation. By integrating the relationship between DNA methylation, gene expression, and PrCa risk using multi-omics data from different sources, we were able to identify consistent associations of the DNA methylation–gene expression–PrCa risk pathway. This supports a very interesting hypothesis that methylation at selected CpG sites could influence PrCa risk through the regulation of expression of adjacent target genes, which warrants further investigation. The current work generates a list of promising CpG sites showing an association with PrCa, which can be investigated further in future studies that directly measure levels of these CpG sites. Identification of circulating DNA methylation biomarkers could be useful for PrCa risk assessment.

In conclusion, in a large-scale study to evaluate associations between genetically predicted DNA methylation levels and PrCa risk, we identified 759 CpG sites that showed an association, including 15 at novel loci, and an additional 63 that represent association signals independent of known risk variants. We also observed that specific CpG sites may influence PrCa risk via regulating expression of candidate PrCa target genes. Further investigation of these findings will provide additional insight into the biology and genetics of PrCa, as well as facilitate risk assessment of PrCa.

## Methods

### Study design

The overall study design is shown in Fig. 2. First, we built comprehensive genetic prediction models for DNA methylation levels by using data of the Framingham Heart Study (FHS). After external validation, we selected methylation models with satisfactory prediction performance for association analyses of genetically predicted methylation levels with PrCa risk, by using data of the PRACTICAL consortia which involves 79,194 cases and 61,112 controls. For CpG sites showing an association with PrCa risk, we assessed associations of their methylation with expression of adjacent genes (FHS, N = 1367), to identify potential target genes of these CpG sites. For the suggested candidate target genes, we further assessed associations of their genetically predicted expression with PrCa risk.

### Building of DNA methylation prediction models

We obtained the individual level genome-wide genotyping and white blood cell DNA methylation data from the FHS Offspring Cohort (dbGaP accession numbers: phs000342 and phs000724). The details of the FHS Offspring Cohort have been described elsewhere36. In brief, DNA was genotyped using the Affymetrix 500 K array, and DNA methylation was profiled using the Illumina HumanMethylation450 BeadChip. The genotype data were imputed to the Haplotype Reference Consortium reference panel37. SNPs with high imputation quality (R2 ≥ 0.8), minor allele frequency ≥0.05, included in the HapMap Phase 2 version, and those that were not strand ambiguous were used to build DNA methylation prediction models. For DNA methylation data, the “minfi” package38 was used to filter out low-quality samples, exclude low-quality methylation probes, estimate cell-type composition, and calculate methylation beta values. We performed quantile normalization to bring the methylation profile of each sample to the same scale, and rank normalization for each CpG site to map each set of DNA methylation values to a standard normal. We adjusted for age, sex, six cell-type composition variables, and the top ten principal components (PCs) derived from genotype data. Genetic and DNA methylation data from 1595 genetically unrelated subjects of European descent were used to build DNA methylation prediction models for this study.

For each CpG site, we built a genetic model to predict DNA methylation levels using the elastic net method as implemented in the “glmnet” package of R, with α = 0.539,40,41 (Supplementary Software 1). Genetic variants flanking a 2-Mb window of each CpG site were used to build the model. Tenfold cross-validation was used for internal validation. Prediction R2 values, the square of the correlation between predicted and measured methylation levels, were used to estimate the model prediction performance.

### External validation of the models

To further evaluate the validity of the built methylation prediction models, we performed external validation using data from 883 unrelated healthy female participants of European descent included in The Women’s Health Initiative (WHI) (dbGaP accession numbers: phs000315, phs000675, and phs001335). Genotype data and white blood cell DNA methylation data were processed using a similar approach, as described above. The predicted DNA methylation for each CpG site was calculated using the models that were established using FHS data, and then compared with the measured level using Spearman’s correlation.

### Associations between predicted methylation and PrCa

Considering that our model external validation dataset WHI included females only, and that there is a high concordance of the model performance (R2) in FHS and WHI, we included DNA methylation prediction models (1) with a R2 ≥ 0.01 (≥10% correlation between predicted and measured methylation levels) in FHS, a standard criterion used in TWAS for gene expression27,39,42,43,44, heritability of which tends to be similar to that of DNA methylation in blood31,45, and (2) for probes with no SNPs within the probe-binding site, considering that the measurement of DNA methylation levels for such probes tends to be unbiased46. Overall, we evaluated associations between genetically predicted methylation levels of 77,243 CpG sites with PrCa risk.

We estimated the association between genetically predicted DNA methylation levels and PrCa risk using S-PrediXcan, which has been described elsewhere47 (Supplementary Software 1). We used the summary statistics data for the association of genetic variants with PrCa risk that had been generated from 79,194 PrCa cases and 61,112 controls of European ancestry in the PRACTICAL, CRUK, CAPS, BPC3, and PEGASUS consortia26,48. In brief, 46,939 PrCa cases and 27,910 controls were genotyped using OncoArray, which included 570,000 SNPs (http://epi.grants.cancer.gov/oncoarray/). Also included were data from several previous PrCa GWAS of European ancestry: UK stage 1 and stage 2, CaPS 1 and CaPS 2, BPC3, NCI PEGASUS, and iCOGS. These genotype data were imputed using the June 2014 release of the 1000 Genomes Project data as reference. Logistic regression summary statistics were then meta-analyzed using an inverse variance fixed effect approach.

A Bonferroni-corrected threshold of P < 6.47 × 10−7 (0.05/77,243) was used to determine a statistically significant association. For CpG sites showing a significant association between genetically predicted methylation levels with PrCa risk, we further evaluated whether the observed associations were independent of nearby PrCa risk variants identified in GWAS or fine-mapping studies, by performing GCTA-COJO analysis49. For this analysis, the risk SNP showing the most significant association with PrCa risk in the PRACTICAL, CRUK, CAPS, BPC3, and PEGASUS consortia was adjusted for calculating association betas and standard errors of DNA methylation predicting SNPs with PrCa risk. These association statistics were then used for re-running the S-PrediXcan analyses.

### Familial relative risk of PrCa explained by novel CpG sites

For PrCa-associated CpG sites that were located at novel loci or independent from known PrCa risk variants, we used the linkage disequilibrium (LD) score regression method50 to evaluate the proportion of familial relative risk of PrCa that could be explained by predicted methylation levels of these CpG sites. In brief, we firstly applied the prediction models of these CpGs to the genetic data of male controls included in the pancreatic cancer GWAS data (N = 3655) to generate the predicted methylation of these CpGs for each of the participants. Detailed information for this dataset, quality control, and imputation has been described elsewhere51. We further used the formula Z2 = 1 + (NTl/M)/$$h$$2 to estimate the heritability explained by these CpG sites. Here for each CpG, Z represents the Z score of the association between the predicted methylation and PrCa risk; NT represents the number of individuals included in the GWAS of the PRACTICAL, CRUK, CAPS, BPC3, and PEGASUS consortia, namely, 140,306; l represents the LD score of the CpG of interest; M represents the number of CpG sites that were significantly associated with PrCa risk; and $$h$$2 is the estimated heritability of PrCa risk that could be explained by the predicted methylation of the CpG sites of interest. The LD score for each CpG was estimated by adding up the squared Pearson correlation coefficient (R2) of the CpG of interest with all the other CpG sites. Finally, after fitting a linear regression model using data of all these CpGs, the estimated heritability of PrCa risk that could be explained by the predicted methylation of the CpGs of interest, along with the standard error and P value, were estimated. Given that the heritability of PrCa was estimated to be 57%52, the familial relative risk of PrCa that could be explained by predicted methylation levels of these CpGs was calculated as 2/0.57.

### Validation of identified CpG sites using the UK Biobank

Individual level data of the UK Biobank were used to validate the identified associated CpG sites. The UK Biobank released GWAS data on ~500,000 individuals53. PrCa cases were determined by combining Hospital Episode Statistics (HES) data and self-reported data. Specifically, cases were defined as hospital admission, type of cancer, or cause of death due to ICD-9 185.9 or ICD-10 C61 or a self-reported cancer code. We calculated associations of genetically predicted DNA methylation of the identified CpG sites with PrCa risk, adjusting for age, age2, and top 20 PCs provided by the UK Biobank. As the number of cases in the UK Biobank is substantially smaller than that in the PRACTICAL, CRUK, CAPS, BPC3, and PEGASUS consortia, we used results from the UK Biobank to confirm the validity of the CpG sites identified in analyses of the consortia data, instead of using their results to filter out CpG sites.

### Functional annotation of PrCa-associated CpG sites

We annotated the position and genomic region information of the identified PrCa-associated CpG sites through ANNOVAR54. The CpG sites were annotated into one of 13 functional categories, including exonic, intronic, intergenic, upstream, 3′-UTR, 5′-UTR, ncRNA intronic, ncRNA exonic, splicing, downstream, upstream/downstream, 5′-UTR/3′-UTR, and exonic/splicing. We used eFORGE55 v1.2 to assess whether the identified CpG sites were enriched in DNase I hypersensitive sites (DHSs) and loci overlapping with various histone modification types, such as H3K27me3, H3K36me3, H3K4me3, H3K9me3, and H3K4me1, across different tissues and cell lines available in the Roadmap Epigenomics Project56, the Encyclopedia of DNA Elements (ENCODE)57 and the BLUPRINT Epigenome58. For each CpG site set of interest, eFORGE performs an overlap analysis against the functional elements for each tissue or cell line separately, and then counts the number of overlaps. A background distribution of the expected overlap counts for the CpG site set of interest is obtained by picking sets of CpG sites with the same number as the test set, matched for gene relationship and CpG island relationship annotation. The matched background sets are then overlapped with the functional elements and the background distribution of overlaps are determined. 1000 matched sets are used. The enrichment value for the test set is expressed as the -log10(binomial P value). Enrichments outside the nominal 95th and 99th percentile of the binomial distribution (after Benjamini–Yekutieli multiple testing correction) are considered significant. We also evaluated whether the associated CpG sites were enriched in loci of genes encoding transcription factors59.

### Determine genes associated with identified CpG sites

For CpG sites with genetically predicted DNA methylation levels significantly associated with PrCa risk, we evaluated associations between methylation and expression levels of genes flanking their loci by using data from the FHS Offspring Cohort (dbGaP accession numbers: phs000363 and phs000724) and The Cancer Genome Atlas (TCGA). Details of the FHS Offspring Cohort, DNA methylation, and gene expression data have been described elsewhere36,60,61. Overall, DNA methylation and gene expression data were available for 1367 unrelated individuals. For the CpG sites showing a significant association with PrCa risk, associations between the normalized methylation levels in beta values and normalized expression levels of genes flanking the CpG sites were estimated, after adjusting for age, sex, top PCs, and estimated cell-type compositions based on methylation data. We further assessed significant methylation–gene expression associations identified in blood tissue analyses in adjacent normal prostate tissue of PrCa patients in the TCGA (N = 34). The processing of DNA methylation and gene expression data has been described elsewhere62,63.

### Associations of potential target genes with PrCa risk

For genes whose expression levels were associated with DNA methylation levels, we assessed whether the genetically predicted expression levels of these genes in blood and prostate tissue were also associated with PrCa risk44,64,65. We used prediction models developed using the PrediXcan method (Elastic Net) and leveraging data from the v8 version of the Genotype-Tissue Expression dataset (GTEx) project (http://predictdb.org/). Details of the methods of building gene expression prediction models using SNPs have been described elsewhere44,47,66. The prediction models were used to estimate the associations between genetically predicted gene expression levels and PrCa risk in the PRACTICAL, CRUK, CAPS, BPC3, and PEGASUS consortia using S-PrediXcan47.

### Associations showing a consistent direction of effect

We assessed the associations between genetically predicted DNA methylation levels and PrCa risk, associations between DNA methylation and gene expression levels, and the associations between genetically predicted gene expression and PrCa risk to assess associations showing consistent direction of effect for the DNA methylation–gene expression–PrCa risk pathway. This could indicate the possibility that genetically predicted DNA methylation might putatively influence PrCa risk through the regulation of expression of flanking target genes.

### Functional enrichment analysis

We performed functional enrichment analysis for the identified genes consistent with the DNA methylation–gene expression–PrCa risk pathway. Canonical pathways, top associated diseases and biofunctions, and top networks associated with these genes were estimated using IPA software28.

### Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

## Data availability

The OncoArray genotype data and relevant covariate information (i.e., ethnicity, country, principal components, etc.) for prostate cancer study are available in dbGAP (Accession no.: phs001391.v1.p1). In total, 47 of the 52 OncoArray studies, encompassing ~90% of the individual samples, are available. The previous meta-analysis summary results and genotype data are currently available in dbGaP (Accession no.: phs001081.v1.p1). The datasets of FHS Offspring Cohort and WHI are publicly available via dbGaP (www.ncbi.nlm.nih.gov/gap): dbGaP Study Accession: phs000342 and phs000724 for FHS, and phs000315, phs000675, and phs001335 for WHI. TCGA data can be accessed through the Genomic Data Commons Data Portal.

## Code availability

The relevant codes are available in the Supplementary Software 1.

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## Acknowledgements

The authors thank Wanqing Wen of the Vanderbilt University School of Medicine for his help with this study. The authors also would like to thank all of the individuals for their participation in the parent studies and all the researchers, clinicians, technicians and administrative staff for their contribution to the studies. This study used resources at the Advanced Computing Center for Research and Education (ACCRE) at Vanderbilt University, Nashville, TN (NIH S10 Shared Instrumentation Grant 1S10OD023680-01 (Meiler). A full description of funding and acknowledgments for the PRACTICAL, CRUK, BPC3, CAPS, and PEGASUS consortia are included in the Supplementary Note. Lang Wu is supported by the University of Hawaii Cancer Center Seed Grant. Yanfa Sun is partially supported by the Department of Education of Fujian Province, P R China.

## Author information

Authors

### Contributions

J.L. and W.Z. conceived the study. L.W. and Y.Y. contributed to the study design. L.W. performed statistical analyses and wrote the paper, with significant contributions from Y.Y. and J.L. X.G. contributed to study discussion. C.W., J.B.N., Y.S., and J.Z. contributed to statistical analyses. X.-O.S., Q.C., X.S., B.L., R.T., M.J.R., G.G.G., H.B., E.M.J., J.C., E.M.G., J.Y.P., J.L.S., Z.K.-J., C.A.H., R.A.E., and W.Z. contributed to paper revision and/or PRACTICAL data management. The PRACTICAL, CRUK, BPC3, CAPS, and PEGASUS consortia investigators contributed to the collection of the data and biological samples for the original studies. All authors have reviewed and approved the final paper.

### Corresponding authors

Correspondence to Lang Wu or Jirong Long.

## Ethics declarations

### Competing interests

R.A.E. has received speakers bureau honoraria and has provided expert testimony for GU-ASCO, RMH FR MTG, and the University of Chicago. The remaining authors declare no competing interests.

Peer review informationNature Communications thanks Francesca Demichelis and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Wu, L., Yang, Y., Guo, X. et al. An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk. Nat Commun 11, 3905 (2020). https://doi.org/10.1038/s41467-020-17673-9

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• DOI: https://doi.org/10.1038/s41467-020-17673-9