DNA methylation and cis-regulation of gene expression by prostate cancer risk SNPs
Authors:
James Y. Dai aff001; Xiaoyu Wang aff001; Bo Wang aff003; Wei Sun aff001; Kristina M. Jordahl aff001; Suzanne Kolb aff001; Yaw A. Nyame aff001; Jonathan L. Wright aff001; Elaine A. Ostrander aff005; Ziding Feng aff001; Janet L. Stanford aff001
Authors place of work:
Division of Public Health Sciences, Fred Hutchison Cancer Research Center, Seattle, Washington, United States of America
aff001; Department of Biostatistics, University of Washington School of Public Health, Seattle, Washington, United States of America
aff002; Department of Laboratory Medicine, Shanghai Children’s Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China
aff003; Department of Urology, University of Washington School of Medicine, Seattle, Washington, United States of America
aff004; Cancer Genetics and Comparative Genomics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland, United States of America
aff005; Department of Epidemiology, University of Washington School of Public Health, Seattle, Washington, United States of America
aff006
Published in the journal:
DNA methylation and cis-regulation of gene expression by prostate cancer risk SNPs. PLoS Genet 16(3): e32767. doi:10.1371/journal.pgen.1008667
Category:
Research Article
doi:
https://doi.org/10.1371/journal.pgen.1008667
Summary
Genome-wide association studies have identified more than 100 SNPs that increase the risk of prostate cancer (PrCa). We identify and compare expression quantitative trait loci (eQTLs) and CpG methylation quantitative trait loci (meQTLs) among 147 established PrCa risk SNPs in primary prostate tumors (n = 355 from a Seattle-based study and n = 495 from The Cancer Genome Atlas, TCGA) and tumor-adjacent, histologically benign samples (n = 471 from a Mayo Clinic study). The role of DNA methylation in eQTL regulation of gene expression was investigated by data triangulation using several causal inference approaches, including a proposed adaptation of the Causal Inference Test (CIT) for causal direction. Comparing eQTLs between tumors and benign samples, we show that 98 of the 147 risk SNPs were identified as eQTLs in the tumor-adjacent benign samples, and almost all 34 eQTL identified in tumor sets were also eQTLs in the benign samples. Three lines of results support the causal role of DNA methylation. First, nearly 100 of the 147 risk SNPs were identified as meQTLs in one tumor set, and almost all eQTLs in tumors were meQTLs. Second, the loss of eQTLs in tumors relative to benign samples was associated with altered DNA methylation. Third, among risk SNPs identified as both eQTLs and meQTLs, mediation analyses suggest that over two-thirds have evidence of a causal role for DNA methylation, mostly mediating genetic influence on gene expression. In summary, we provide a comprehensive catalog of eQTLs, meQTLs and putative cancer genes for known PrCa risk SNPs. We observe that a substantial portion of germline eQTL regulatory mechanisms are maintained in the tumor development, despite somatic alterations in tumor genome. Finally, our mediation analyses illuminate the likely intermediary role of CpG methylation in eQTL regulation of gene expression.
Keywords:
DNA methylation – Gene expression – Gene regulation – Variant genotypes – Prostate gland – Benign tumors
Introduction
Prostate cancer (PrCa) is the most common noncutaneous cancer among men in the Western world [1], yet few risk factors have been identified [2]. Twin and familial studies have long established that genetics is a major component of PrCa etiology [3–8]. Tremendous progress has been made by genome-wide association studies (GWAS) to identify genetic loci predisposing to PrCa, and more than 150 PrCa susceptibility SNPs have been identified [9–29]. The most recent and the largest GWAS to date assembled 79,194 cases and 61,112 controls of European ancestry from 59 studies for genotyping on a custom high-density genotyping array (the OncoArray), identified 62 novel loci associated with overall PrCa risk [29]. The polygenic risk score using the more commonly occurring 147 PrCa risk SNPs (S1 Table) captured 28.8% of the familial relative risk, which may provide a useful tool to identify men at higher risk for PrCa. Despite the remarkable progress in identifying PrCa risk SNPs, functional interpretation of risk SNPs presents a huge challenge. As Fig 1 shows, 141 out of the 147 PrCa risk SNPs (96%) are located in noncoding regions of the human genome, and five of six risk SNPs located in coding regions are nonsynonymous. The biological mechanisms of these SNPs influencing the risk of PrCa remain largely unknown.
A common strategy to interpret functional activity of GWAS-identified risk SNPs is to investigate whether they affect gene expression [30–33]. Such genetic determinants are referred to as expression quantitative trait loci (eQTLs), influencing mostly local genes in nearby genomic regions (local eQTLs, or cis-eQTLs for convenience, without requiring evidence of allelic effects at each locus). Large consortia such as the Genotype Tissue Expression project (GTEx) now provide genome-wide eQTL mapping from normal whole blood samples and multiple organs [34,35]. Evidence is abundant that trait-associated SNPs are more likely to be eQTLs [36], and eQTLs are pervasive in the human genome. A substantial number of eQTLs in the human genome are tissue-specific, and sample size is a major determinant of the number of eQTLs that can be detected at genome-wide significance [35]. Yet the number of normal prostate samples in GTEx is limited due to the difficulty of obtaining normal prostate samples from donors. A large-scale prostate-specific eQTL analysis from the Mayo Clinic was conducted in 2015 using 471 adjacent histologically benign prostate tissue samples from prostate cancer patients [37], reporting that nearly half of the known PrCa risk loci/regions may harbor cis-eQTLs. As eQTLs are often dependent on tissue type and developmental stage, it is anticipated that eQTLs will differ between primary prostate tumor tissue and adjacent benign tissue from the same prostate, though there has not been a systematic comparison of eQTLs and associated genes (referred to as eGenes hereafter) for the most recent set of GWAS loci between primary prostate cancer samples and tumor-adjacent benign prostate samples. The differences in eQTL associations may reflect molecular alterations that occur during carcinogenesis. An investigation of eQTLs among 12 known PrCa risk loci in 2012 identified four cis-QTLs in benign tissues and these associations tended to be more attenuated in tumors [38]. Another eQTL study in 2015 examined 39 PrCa risk loci and differences of associations between tumor and adjacent benign samples [39].
While a great deal of progress has been made in identifying eQTLs in the human genome, epigenetic mechanisms for regulating gene expression, e.g., DNA methylation, histone modification, and chromatin accessibility, are less understood [40,41,42]. In particular, DNA methylation at CpG sites is an essential epigenetic mark that links to cellular differentiation and tissue development. Aberrant DNA methylation has been long recognized to be associated with human diseases, including cancers [43]. This is particularly of interest to prostate cancer, as DNA methylation plays a critical role in developing prostate cancer, and epigenome continues to evolve throughout the life history of prostate cancer, possibly associated with cancer outcome [44]. Genetic polymorphisms such as SNPs have been shown to contribute to variations of DNA methylation in blood, brain, and adipose tissue and are referred to as methylation-QTLs (meQTLs) [45–49]. Interestingly, accumulating evidence from peripheral blood samples suggests that eQTLs co-localize with meQTLs in the genome [41,50–52], and genetic control of DNA methylation and gene expression may have a shared, causal component [53]. Dissecting the direction of causality presents challenge to statistical analysis: DNA methylation could be associated with SNPs independent of an effect on gene expression, or actively mediate the eQTL effect on gene expression, or play a passive role in gene regulation as a downstream event. The Mendelian randomization approach has been used in this context, which assumes that the genetic effect on an outcome goes through the intermediary in its entirety and therefore cannot test against the independence relationship [54]. The Causal Inference Test (CIT) can test the causal direction in principle, using the conditional independence relationship of three variables in a causal pathway and simultaneously assessing multiple causal parameters in the pathway models [55]. However in practice it can produce significance for both mediation and reverse causation, rendering results uninterpretable [55]. To date, no meQTL mapping study has been reported on prostate tumor samples or histologically benign prostate samples, nor has any study disentangled the relationships between eQTLs, DNA methylation and gene expression in prostate tissue samples.
In this work, we perform a comprehensive eQTL and meQTL analysis for 147 PrCa risk SNPs using genomic data from two large sets of primary prostate tumor samples (Fred Hutchinson Cancer Research Center, FH, n = 355; and The Cancer Genome Atlas, TCGA, n = 495) and a large set of histologically benign prostate samples from cancer patients (Mayo Clinic, n = 471). Focusing on established PrCa risk SNPs, the goal of this analysis is three-fold: to identify and compare eQTLs in tumor-adjacent benign samples and primary prostate tumors, to identify meQTLs in tumor-adjacent benign samples, and to investigate through data triangulation the causal role of DNA methylation in genetic regulation of gene expression. Genes found to be under regulation of the PrCa risk SNPs will be characterized by Ingenuity Pathway Analysis (IPA). To interpret eQTLs in the context of cancer development, we also analyze data from 50 pairs of tumor and tumor-adjacent, histologically benign samples from TCGA.
Results
Overview of samples and datasets
Fig 2 shows samples, datasets and goals for this analysis. We have included two large sets of primary prostate tumors, both of which have data available on genome-wide genotypes, gene expression and DNA methylation: the first set is from a FH-based cohort of PrCa patients diagnosed with clinically localized stage disease (n = 355), and the second set is the comprehensive genomic data for primary PrCa samples publicly available from TCGA (n~500). Both eQTL mapping and meQTL mapping were conducted in the two tumor datasets. The role of DNA methylation in genetic regulation of gene expression was investigated. For comparison of eQTLs, we have included a previously published set of tumor-adjacent, histologically benign samples from men with PrCa who were treated at the Mayo Clinic (n = 471), which had genome-wide genotypes and gene expression data. The fourth set is the tumor-adjacent, histologically benign samples from TCGA (n = 50), which were compared to the matched TCGA tumor samples, in order to explore whether somatic alterations may explain the differences of eQTL/meQTL mapping results in tumors and in adjacent benign samples. Note that although previous eQTL studies referred to tumor-adjacent, histologically benign samples from cancer patients as “normal” prostate samples [37,38,39], the field effects on somatic alterations (DNA methylation in particular) have been reported [56,57,58]. We therefore referred to the tumor-adjacent samples used in this work hereafter as “benign samples”.
Cis-eQTL and associated eGenes for 147 PrCa risk SNPs
We first cataloged the total number of possible cis-eQTLs for the 147 PrCa risk SNPs, when considering all genes within 1 Mb of each risk SNP. There are 3089 SNP and gene pairs in the Mayo Clinic adjacent benign prostate tissues (n = 471), 3300 pairs in the FH tumor tissues (n = 355), and 3468 pairs in TCGA tumor tissues (n = 492). The different numbers of pairs are due to the different gene expression platforms (gene-expression array for FH samples, and RNA-seq for Mayo and TCGA samples). Fig 3A shows the quantile-quantile plots of p-values resulting from cis-eQTL mapping in the three datasets. The eQTL data from the Mayo adjacent benign tissues yielded many more significant p-values than the two tumor datasets, likely due to more eQTLs in histologically benign (non-cancerous) samples. Using the false discovery rate of 0.05 as the significance threshold, Table 1 shows that there are 259 eQTL-eGene pairs (98 eQTL SNPs and 250 eGenes) detected in the Mayo samples, 75 eQTL-eGene pairs (48 eQTL SNPs and 73 eGenes) in the TCGA samples, and 43 eQTL-eGene pairs (34 eQTL SNPs and 42 eGenes) in the FH samples. The details of the significant results for eQTL mapping are shown in S2 Table. The identified eQTLs typically explain a small proportion of gene expression variability: the median R-square for eQTLs in the three datasets is 0.069 (FH), 0.043 (TCGA), and 0.036 (Mayo), respectively.
In the Mayo adjacent benign samples, 60% of cis-eQTLs were associated with at least two eGenes (median of the number of eGenes associated with an eQTL = 2, max = 12). On average, fewer eGenes were associated with an eQTL in tumor samples (TCGA: median = 1, max = 7, 17 eQTLs associated with more than 1 eGene; FH: median = 1, max = 3, 7 eQTLs associated with more than 1 eGene), suggesting that eQTL regulation may be disrupted in tumors. The top master regulators of gene expression are rs3129859 and rs3096702 from the HLA region in chromosome 6, which are associated with 2 and 9 eGenes in the Mayo set, 7 and 3 eGenes in the TCGA set and 1 and 2 eGenes in the FH set.
A substantial number of eQTLs overlapped between the FH data (19 out of 34) and TCGA data (19 out of 48). The discrepancy between eQTLs found in the two tumor datasets may be explained by differences in sample types used to extract mRNA (FFPE for FH and fresh frozen for TCGA), gene expression profiling methods (microarray for the FH samples and RNA-seq for the TCGA samples) so that some gene expressions are only available in one dataset but not the other, sample sizes and clinical characteristics (TCGA over-sampled high Gleason score tumors and therefore is less representative of primary tumors). Indeed, if one of the two tumor datasets were used as the discovery set (FDR<0.05) and the other dataset as the validation set (p-value <0.05), 25 out of the 34 eQTLs (74%) identified in the FH data were validated by the TCGA data, and 28 out of the 48 eQTLs (58%) identified in the TCGA data were validated in the FH data. Across the two tumor datasets, 39 pairs (34 eQTLs and 37 eGenes) had FDR<0.05 in one dataset and a p-value <0.05 in the other dataset. We therefore define this set of 39 pairs to be the PrCa eQTL-eGene pairs and compare them with the eQTL-eGene pairs in the adjacent benign samples.
We investigated the discrepancy between the FH and TCGA set. For the nine eQTLs and associated 16 eGenes identified in FH but not in TCGA, ZAK (paired with rs34925593) and HCG4P6 (paired with rs12665339) were not available in the TCGA dataset. As the result, two eQTLs- rs34925593 and rs12665339-couldn’t be detected in the TCGA dataset. The rest of 7 eQTLs were associated with 13 eGenes, which were available and expressed in both tumor sets. For the 20 eQTLs and associated 42 eGenes identified in TCGA but not FH, ZFP57 (paired with rs7767188), TRIM26 (paired with rs7767188), MRM2 (paired with rs527510716), CLDN25 (paired with rs11214775), and ZNF652 (paired with rs11650494) were not available in the FH dataset. As the result, the four eQTLs (rs7767188, rs527510716, rs11214775 and rs11650494) were not detectable in the FH dataset. The rest 16 eQTLs were paired with 37 eGenes which were available and expressed in the FH dataset. These results suggest most of the discrepancy between eQTLs in FH and eQTLs in TCGA is likely due to differences of sample size and cancer clinical characteristics.
Fig 3B shows the Venn diagrams for the eQTLs and e-Genes identified in the Mayo adjacent benign samples and the tumor samples. One striking finding is that most of the eQTLs identified in prostate tumors were also found in the adjacent benign samples (33 in 34 eQTLs detected in tumors), the majority of eGenes in tumors were also identified in the histologically benign samples, while 34% of 98 eQTLs in the Mayo adjacent benign samples were also detected in tumor samples, suggesting that there were very few tumor-specific eQTL-eGenes. When eQTLs in FH and eQTLs in TCGA were separately compared to eQTLs in Mayo adjacent benign samples, there are 28 eQTLs shared between FH and Mayo, 38 eQTLs shared between TCGA and Mayo. The tumor-specific eQTL-eGene pairs were plotted in S1 Fig. The majority of the tumor-specific eQTLs are likely due to random noise when genotypes only explain a small portion of the variability in gene expressions, so that some SNPs not associated with gene expressions in the benign samples showed a somewhat moderate level of, sometimes inconsistent, association in the two tumor sets (S1 Fig). The difference between the tumor and adjacent normal set is not attributed to the difference of gene-expression platforms. Among 65 eQTL identified in adjacent normal but not in tumor samples, two eQTLs (rs1465618 and rs10086908) have eGenes (LOC100129726 and PCAT1) not available in both the tumor datasets, and 4 eQTLs (rs4713266, rs527510716, rs1512268, rs8008270) have associated eGenes (SMIM13, MRM2, NKX3-1, GNPNAT1) not available in the FH dataset only.
Fig 3C shows the general concordance between effect sizes of SNP-gene associations in TCGA tumors and effect sizes of SNP-gene associations in Mayo benign samples, for all SNP-gene pairs and for the significant eQTL-eGene pairs in both sets. This result suggests that the majority of eQTL regulatory mechanisms in the benign samples are largely intact in tumors, though tumor eQTLs may have smaller effect sizes due to other somatic alterations such as mutations, copy numbers and DNA methylation. Fig 3D shows three representative examples of the most significant eQTL-eGenes, confirming previously reported eQTL mapping results. One pair (rs12653946-IRX4) was identified in both tumor and tumor-adjacent benign samples, one (rs4430796-HNF1B) was only identified in adjacent benign samples, and the last in tumors only (rs11135910-EBF2). Interestingly, all three eGenes encode transcription factors and are believed to be tumor suppressor genes [59–63]. The association of rs1265394 and IRX4 transcript has been reported previously in Japanese and European populations [59,64]. HNF1B is a member of the homeodomain-containing superfamily of transcription factors that may suppress epithelial-to-mesenchymal transition (EMT) in unmethylated, healthy tissues. This tumor-suppressor activity is lost when HNF1B is silenced by promoter methylation in the progression to PrCa [61]. It may also be involved in PrCa development via modulating androgenic hormone effects [62]. Consistent with our result, a previous eQTL analysis also reported the eQTL association for rs4430796-HNF1B only in tumor-adjacent, histologically benign prostate tissue but not in tumors [38]. The oncogenic role of EBF2 in PrCa development is less understood [63], though this eQTL association of rs11135910 with EBF2 has been reported earlier in a smaller subset of TCGA data [65].
Using IPA, a gene set enrichment analysis for the 250 eGenes identified in the Mayo adjacent benign samples was conducted. As the background in these genomic regions, the canonical pathways, molecular functions, and networks enriched by these eGenes were compared to those derived from 2417 genes in the cis regions which were not identified to be eGenes of the 147 PrCa risk SNPs. The top ten canonical pathways are all immune—related functions, such as antigen presentation (p-value = 2.2e-10), PD-1, PD-L1 cancer immunotherapy pathway (p-value = 2.0e-7), and allograft rejection signaling(p-value = 3.2e-7), and OX40 signaling(p-value = 4.7e-7, S3 Table). This included numerous HLA genes, including HLA-A, HLA-DPB1, HLA-DQA1, HLA-DQA2, HLA-DQB1, HLA-DQB2, HLA-DRB1, HLA-DRB5, HLA-G. These HLA genes are associated with five PrCa risk SNPs in chromosome 6: rs7767188, rs12665339, rs3096702, rs3129859, and rs9296068. The top enriched molecular and cellular functions for these 250 eGenes are important for cell to cell signaling and interaction (24 genes),cell cycle (24 genes), cell morphology (21 genes), cellular development, cellular growth and proliferation (19 genes), and immunological disease (17 genes). The largest molecular functional group are genes related to DNA transcription, including the ones shown in Fig 3d and 3a number of well-known transcription regulators and DNA methylation machineries, such as ASCL2, FOXP4, TET2, DNMT3B, HNF1B, HOXA13, NOTCH4, IRX4, CTBP2, and ZNF217. Notably, TET2 (corresponding eQTL rs7679673) encodes a methylcytosine dioxygenase that catalyzes the conversion of methylcytosine to 5-hydroxymethylcytosine and plays an important role in DNA demethylation. It has been reported that TET2 binds the androgen receptor and its loss is associated with prostate cancer [66]. DNMT3B (corresponding eQTL rs11480453) encodes a DNA methyltransferase which is thought to function in de novo methylation and have been implicated in prostate cancer development [67]. Genes involved in steroid synthesis included CYP21A2, HSD17B2, ITGA6, IDI2, MAP2K1, PMVK, TSPO, and may correspond to androgen dependent growth of prostate cancer.
cis-meQTLs and associated CpGs for 147 PCa risk SNPs
Within 1 Mb distance of the 147 PCa risk SNPs, 77,649 SNP-CpG pairs were identified in the FH data and 69,602 SNP-CpG pairs in the TCGA data. Cross-reactive and polymorphic CpGs were removed in both datasets. The different numbers of SNP-CpG pairs between the two datasets are due to removal of CpGs in the TCGA dataset that are located within 15bp of a repetitive element. Fig 4 shows the summary of cis-meQTL mapping results. The details of the significant results for cis-meQTL mapping are shown in S2 Table. The q-q plot in Fig 4A highlights the large number of significant SNP-CpG pairs for both datasets. Table 2 summarizes the cis-meQTL mapping results. When FDR <0.05 was used as the significance threshold, approximately two-thirds of the 147 PCa risk SNPs were identified as meQTLs in at least one of the two tumor datasets. There are 776 meQTL-CpG pairs (101 meQTLs and 740 CpGs) identified in the TCGA data, and 586 meQTL-CpG pairs (93 meQTLs and 567 CpGs) identified in the FH data. The median distance between the chromosomal positions of meQTLs and their associated CpGs is 52,747 bp (min = 9, max = 956,913) in the FH dataset, and 67,139 bp (min = 11, max = 985,743) in the TCGA dataset. Similar to eQTLs, meQTLs typically explain a small proportion of the variability of CpG methylation levels: the median R-square for meQTLs in the FH dataset is 0.056, and the median R-square for the meQTLs in the TCGA data is 0.046. The functional annotation of the CpGs linked to meQTLs shows that in the FH data, 13% of the CpGs are located in promoters, 37% in gene bodies (between transcription start site and transcription ending site), and 21% in enhancer regions. In the TCGA data, 16% of the CpGs are located in promoters, 37% in gene bodies, and 17% in enhancer regions. The spatial distribution of these CpGs linked to meQTLs did not differ significantly from all CpGs included on the HM450 array.
Typically, meQTLs are associated with multiple CpGs (median = 2, min = 1, max = 91 in the FH data, and median = 3, min = 1, max = 110 in the TCGA data). These meQTLs may be master regulators of DNA methylation that involves multiple genes. Among 93 meQTLs identified in FH, 26 of them are associated with multiple CpGs which are located in more than one gene. Among 101 meQTLs identified in TCGA, 33 of them are associated with multiple CpGs which are located in more than one gene. Notably, we found the three PrCa SNPs in chromosome 6 (rs7767188, rs3129859 and rs3096702) are master regulators of DNA methylation in over 9 genes in near regions. All three SNPs are also identified as eQTLs in TCGA and FH tumor data.
Fig 4B shows that meQTLs (with FDR <0.05) identified in the two datasets are highly concordant, with 71 meQTLs (76% of FH meQTLs) being shared. The concordance increases to 85 meQTLs (91% of FH meQTLs) if we use a less stringent significance rule: FDR <0.05 in one dataset and p-value <0.05 in the other. This level of consistency is much higher than the eQTL findings in the two datasets, which may be attributed to the better preservation of DNA than RNA in FFPE tumor tissue samples, and the fact that the same profiling method was used for measuring DNA methylation (Illumina HM450 BeadChip).
Fig 4C shows an example of meQTL-CpGs appearing in both the FH and TCGA sets. SNP rs141536087 is located in the gene-body of LARP4B, and cg26597838 is located in an enhancer region approximately 17 Kb upstream of LARP4B. LARP4B is an RNA binding protein that has been previously identified as a putative tumor suppressor that inhibits cell migration and invasion of prostate cancer cells [68]. Furthermore, rs141536087 is an eQTL for LARP4B in the Mayo set (p-value = 4.5e-15) but not in the two cancer sets (p-value = 0.41 for FH and 0.63 for TCGA).
Relationship between cis-eQTL and cis-meQTL
Fig 5 includes the Venn diagram of eQTLs and meQTLs identified in the two tumor datasets. The majority of eQTLs are also meQTLs in tumor datasets (Fig 5A and 5D), more so in the TCGA data (30 out of 34 in the FH data; 41 out of 48 in the TCGA data), while only ~41% of meQTLs are also eQTLs in the TCGA data, and ~32% of meQTLs are also eQTLs in the FH data. One complicating factor for comparing eQTLs and meQTLs is that there were more pairs being tested for meQTL than eQTL pairs, therefore meQTL mapping is penalized by a greater degree of multiple testing correction. If a less stringent significance threshold (FDR <0.2) is used for meQTL mapping, 44 out of 48 eQTLs identified in the TCGA data are also meQTLs, and 32 out of 34 eQTLs in the FH data are also identified as meQTLs, reinforcing the finding that eQTLs is mostly a subset of meQTL in tumor sets.
For those SNPs identified as both eQTL and meQTL, causal effects of the associated CpG methylation sites on the corresponding gene expressions were assessed for 541 SNP-CpG-gene expression triplets (31 SNPs, 385 CpGs, 39 genes) in the FH set and 1219 SNP-CpG-gene expression triplets (41 SNPs, 539 CpGs, 72 genes) in the TCGA set, using the Mendelian randomization (MR) method exploiting genetic variants as instrumental variables. Fig 5B and 5E show the histograms of p-values derived from the two-stage least squares method for the two tumor sets, both showing a high proportion of triplets with evidence of causal effect (47% triplets in FH have FDR<0.05, 35% triplets in TCGA have FDR<0.05). However, a significant MR result could also due to the genotype affecting DNA methylation and gene expression independently. An alternative method is to assess the dose correspondence of eQTL effect sizes and meQTL effect sizes. The triplets were restricted to those containing CpG sites located in the same genes whose expression was measured (91 in FH and 145 in TCGA), Fig 5C and 5F assess the concordance of the absolute values of genetic associations with standardized CpG methylation levels and the absolute values of genetic associations with standardized gene expression levels. The absolute values of coefficients were plotted because DNA methylation can be positively or negatively associated with gene expression, depending on the locations of the CpGs in a genic region (gene body or promoter). Both scatter plots show the dose response relationship between a SNP’s genetic influence on DNA methylation and on gene expression (p-value for a linear trend is 0.018 for the FH data and 5.1e-7 for the TCGA tumor data), which provides evidence of a causal relationship between DNA methylation and gene expression. Taken collectively, the results in Fig 5C and 5F suggest that genetic regulation of gene expression and genetic regulation of CpG methylation are not independent molecular events, though neither Mendelian randomization nor the dose response can differentiate the direction of the causal effect: it could be that eQTL associations were mediated by altering DNA methylation in the respective genes, or that DNA methylation is a downstream event after a genetic variant affecting gene expression.
Absence of eQTLs in tumor samples may be due to altered DNA methylation
The TCGA genomic data for 50 pairs of primary PrCa and adjacent benign samples were investigated for reasons that may explain the “loss” of eQTLs when comparing tumors to adjacent benign samples. We investigate whether differential gene expression, copy number alterations or somatic mutations between tumor and normal samples where associated with loss of eQTL in tumors. There is no systematic difference for either of three genomic features when we compare 53 genes which lost eQTL control in TCGA tumors to 173 eGenes whose eQTL regulation remain intact in TCGA tumors.
Fig 6 shows the comparison of DNA methylation in the eGenes in adjacent benign samples only and the eGenes in both tumor and benign samples. DNA methylation data available for the paired 50 tumors and 50 tumor-adjacent benign samples were investigated in two ways. First, differentially methylated probes (DMP) between tumor samples and tumor-adjacent, histologically benign samples (paired with matched tumor) were identified in regions surrounding eGenes. There are more differentially methylated probes between tumors and adjacent benign samples around the eGenes that “lost” genetic regulation in tumors from eQTLs compared to eGenes that “maintained” genetic associations in both benign samples and tumor samples (Fig 6A, p-value = 0.032). Second, the differentially methylated region (DMR) between tumor samples and tumor-adjacent, histologically benign samples were determined by at least two consecutive probes with significant differences in the same direction. Fig 6B compares the number of DMRs in two groups of genes: there are more tumor-benign DMRs in the genes which lost genetic regulation in TCGA tumors, with a marginally statistically significant difference (p-value = 0.0612). Finally, the percentage of genes containing at least one meQTL-regulated CpG sites (as defined in the TCGA set in Fig 4) was compared between the two groups of eGenes. Consistently, there was a substantially higher percentage of eGenes in tumor and benign samples which have genetically regulated CpGs, when compared to the eGenes in benign samples only (Fig 6C, 64% vs 26%, p-value = 3.46e-7). In S2 Fig, two examples were shown where eQTL associations were evidently weakened in the tumor data and, simultaneously there are substantial differences between DNA methylation at key CpG sites within the gene between tumors and adjacent benign samples (~50 pairs from TCGA). Together with Fig 5, these results in Fig 6 and S2 Fig suggest the hypothesis that at least some altered CpG methylation sites may be mechanistically involved in loss of genetic regulation of gene expression in tumor sets.
Mediation analysis of genetic influence on DNA methylation and gene expression
To further dissect the direction of causality among the three possible relationships (Fig 7), mediation analyses between PrCa risk SNPs, CpG methylation probes and expressions of eGenes were conducted using the Causal Inference Test (CIT) method [55] and the three additional criteria we propose. CIT is a four-component composite test that was designed to test mediation of the effect of an exposure on an outcome by an intermediate phenotype (see details in the Methods Section). The goal here is to identify three types of mediation relationships: 1) a SNP influences gene expression and DNA methylation through independent pathways (denoted as independence, no causal relationship); 2) a SNP alters CpG methylation, which in turn influences gene expression (SNP→Methylation→Gene, denoted as the SME mediation); and 3) a SNP changes gene expression, which unwind local chromosome and triggers passive alterations in CpG methylation (SNP→Gene→Methylation, denoted as the SEM mediation). See the top panel in Fig 7 for illustration of the three tri-variate relationships. The unique feature is that there will be typically multiple CpG sites involved in any eQTL-eGene pair.
In the TCGA dataset, 41 risk SNPs identified as both eQTL and meQTL were included in the mediation analysis, together with their associated CpG probes and gene expression (72 eGenes, 539 CpG probes). There are 1219 QTL-CpG-Gene triplets, 824 of them have both CIT-SEM and CIT-SME p-values > 0.05, 210 have both CIT p-values <0.05, 185 have one of the two CIT p-values <0.05. Pooling multiple CpGs in the cis-region around a gene together and using CIT and three proposed criteria to differentiate SME and SEM, we identified evidence of SME for 30 QTL-CpGs-Gene relationships, 15 SEM triplets for QTL-Gene-CpGs relationships, and 18 independent QTL-Gene/QTL-CpGs relationships (Fig 7). In the FH dataset, 31 risk SNPs identified as both eQTL and meQTL were included in the mediation analysis, together with their associated CpG probes and gene expression (39 eGenes and 385 CpG probes). There are 541 QTL-CpG-Gene triplets, 394 of them have both CIT-SEM and CIT-SME p-values > 0.05, 99 have both CIT p-values <0.05, 48 have one of the two CIT p-values <0.05. Pooling nearby CpGs, we identified 12 SME triplets, 9 SEM triplets, and 15 independent triplets in the FH set (Fig 7). The two pie plots in Fig 7 shows the distribution of the three relationships. Across the two datasets, over two-thirds of the triplets showed evidence of a causal relationship, the majority of which are SME. The details of mediation results are shown in S4 Table.
Table 3 shows examples of the SNP-CpGs-eGene triplets that were identified to be SME (5 triplets) or SEM (4 triplets), and that were consistent between FH and TCGA datasets. This group of risk SNPs provides the strongest evidence of that regulation of the corresponding eGenes involves alterations of DNA methylation. The majority of these SNPs in Table 3 have been previously reported to be eQTLs for some putative PrCa risk genes, including rs2292884 for MLPH [69], rs12653946 for IRX4 [59,60], rs1933488 for RGS17 [70,71], rs10993994 for MSMB [72,73], rs5945619 for NUDT11 [38,74], Notably, SNP rs684232 has been reported to be associated with FAM57A gene expression [38,39], a gene encoding membrane-associated protein that promotes lung carcinogenesis [75], though its role in PrCa has not been reported. Several pairs of eQTL-eGenes represent new discoveries. SNP rs10875943 is between the tubulin gene TUBA1C and the peripherin gene PRPH. Our result suggests its link to TUBA1C, though its functional role in PrCa has not been studied. The genes in the 6p21/MHC region, HLA-DQB1 and HLA-DRB5, that are associated with rs3096702 and rs3129859, have not been previously studied in relation to PrCa.
A substantial proportion of the mediation relationships for the triplets are inferred to be SME (Fig 7), evidence of the mechanistic role of DNA methylation in the genetic regulation of gene expression. Figs 8 and 9 shows two examples of SME with three diagnostic plots for inferring causal direction: residuals of gene expression~CpGs regression versus genotypes (Figs 8A and 9A), gene expression versus residuals of CpG~genotype regression (Figs 8B and 9B), and residuals of CpG~gene expression regression versus genotypes (Figs 8C and 9C). Associations shown in the last two plots but not the first plot indicate a SME relationship. Specifically, rs12653946 is located in an intronic region of an RNA gene transcribed upstream of IRX4, regulating gene expression of IRX4 [59,60] (Fig 8). Our result suggests that this gene regulation is mediated altered DNA methylation in the CpG islands located in the first exon and the gene body. For the 6p21/MHC region (Fig 9), previously SNP rs3096702 was suggested to be associated with NOTCH4, a nearby gene that may be related to epithelial-mesenchymal transition (EMT) and PrCa growth [76]. Our result suggests that this SNP influences gene expression of an HLA class II gene DQB-1, which may be related to immune escape of PrCa. Furthermore, this genetic influence on gene expression is mediated through multiple CpGs in the gene body and TSS1500 region. The proportion of genetic control on gene expression explained by the CpGs was as high as 50% ~ 100% in the two tumor sets for the two genes. Further inspection of ENCODE data in the 30 kb region surrounding this SNP suggests that rs3096702 is in binding sites for multiple transcription factors and the transcriptional regulator protein CTCF, 300 kb upstream of the HLA gene. These results suggest that rs3096702 may affect transcription binding affinity and enhancer-mediated epigenetic machinery, then regulate the methylation and gene expression of HLA genes.
Discussion
In this work we performed rigorously eQTL and meQTL mapping for the 147 confirmed PrCa risk SNPs using comprehensive genomic data in primary prostate tumors (TCGA and FH) and tumor-adjacent benign samples (Mayo Clinic). To our knowledge this is the first eQTL study for PrCa risk SNPs that also includes DNA methylation data, and the first to systematically investigate the differences of eQTLs in prostate tumors and tumor-adjacent benign samples. Methodologically, we also carefully examined the existing approaches and proposed a modified version of CIT to disentangle the role of DNA methylation in eQTL regulation. The impact of this work is primarily on the prostate cancer literature and the functional interpretation of 147 prostate cancer risk SNPs. The contributions of this work are two folded: we systematically compare eQTLs and meQTLs among prostate cancer tissue and the adjacent normal tissue which has not been done previously; we rigorously dissect the role of DNA methylation in eQTL regulation of gene expression. Several important observations were made as discussed below.
First, perhaps not surprisingly, there are many more eQTLs identified in the tumor-adjacent benign samples than in primary tumor samples. Moreover, nearly all eQTLs in tumors are also identified as eQTLs in tumor-adjacent benign samples, yet approximately half of eQTLs in adjacent benign samples were not present in tumors. This observation is consistent with previous observations that eQTL association signals in normal or benign samples tend to be attenuated in tumor samples [37], if not absent, and benign tissue samples tend to have more eQTLs than tumor samples [77]. One possible explanation for an eQTL only identified in histological benign samples but not in tumors is that the corresponding eGene may only function in tumor initiation, become silenced in tumor progression. For example, our result (Fig 3D) confirmed previous findings that rs4430796 is an eQTL for HNF1B only in the tumor-adjacent benign samples [38,77], but not in tumor samples. Recent functional assays suggest that HNF1B, which encodes a transcription factor, is a pro-differentiation factor that suppresses epithelial-to-mesenchymal transition (EMT) in unmethylated, healthy tissues [61]. This tumor-suppressor activity is lost when HNF1B is silenced by promoter methylation in the progression to PrCa, and it is therefore no longer associated with the eQTL [61]. Along this same line, it is also possible that somatic alterations such as mutations, copy number changes and aberrant DNA methylation arising in the tumor genome perturb gene expression, which may disrupt or weaken eQTL associations. This explanation is consistent with Fig 3C, where there is a global concordance between eQTL effect sizes in benign samples and eQTL effect sizes in tumors. We have thoroughly investigated the TCGA genomic data regarding somatic alterations in the PrCa genome, and we show in Fig 6 that the loss of eQTL regulation in gene expression in tumors may be due to widely altered DNA methylation in tumors, less likely due to somatic mutations or copy-number alterations. On the other hand, we conclude that among the 147 PrCa susceptibility SNPs, tumor-specific eQTLs are very rare, likely because the eQTLs in these susceptibility SNPs predispose to cancer risk through influencing oncogenic genes in benign samples during the early stage of tumor development. One complication factor is the field effect of carcinogenesis–the benign prostate samples are tumor-adjacent, histologically benign, taken from cancer patients. It is possible that gene expression profiles of tumor-adjacent, histologically benign samples have been altered by the tumor field effect.
Second, the majority of the 147 risk SNPs (~100) were identified to be meQTLs in prostate tumors, yet only a subset was identified as eQTLs. Intriguingly, nearly all eQTLs were also identified as meQTLs. It is known that aberrant DNA methylation play a key role in PrCa development, which may interfere with genetic regulation of gene expression. We hypothesize that, if we indeed had a large set of normal prostate samples, we would observe more PrCa SNPs that are meQTLs in normal prostate samples, with a high degree of overlap between eQTLs and meQTLs in normal prostate tissue. This level of concordance is much higher than what was reported in the recent genome-wide analyses of eQTLs and meQTLs from peripheral blood and lymphoblastoid cell lines [48–51], suggesting that genetic regulation of gene expression by these PrCa risk SNPs are very much intertwined with methylation changes, either actively as a mediator or passively as a downstream consequence. Our results in Fig 4 and mediation analyses support this hypothesis. There are several possible explanations for the observation that more risk SNPs are meQTLs than eQTL. It is known that DNA methylation may have broader biological functions in maintaining chromosomal stability and cellular differentiation beyond regulating gene expression. Furthermore, mRNA abundance is much more dynamic, subject to multiple regulating mechanisms and more liable to measurement error when compared to DNA methylation. Therefore, eQTL mapping may be inherently more variable than meQTL mapping. Thus, not all meQTLs become eQTLs in a particular cellular state, similar to the observation that not all differentially methylated CpGs correlates with altered gene expression.
Third, among the risk SNPs that were both eQTLs and meQTLs, our mediation analysis suggests that the majority of triplets (SNP, DNA methylation, gene expression) display a causal mediation relationship, either of SNP→Methylation→Expression (SME) or SNP→Expression→Methylation (SEM), supporting the important role of DNA methylation in PrCa risk SNPs for regulation of gene expression. DNA methylation variable sites are known to be associated with gene expression mechanistically in complex and context-dependent ways, which includes both active (e.g., DNA hypomethylation causally affecting gene expression through transcription factor binding) or passive methods where DNA methylation is a consequence or independent mark of gene expression (e.g., reflecting the chromatin state) [49]. Statistically it is challenging to discern whether DNA methylation status is an active or passive consequence of gene expression. For example, standard CIT could not distinguish the SME from the SEM model in a recent genome-wide eQTL and meQTL analysis.53 Leveraging typically multiple candidate mediating CpG sites in a gene, we have added additional discriminatory criteria to the CIT test in order to separate SME from SEM: 1) the SME p-value is smaller than the SEM p-value, and the proportion of association explained by SME should be greater than SEM; and 2) the proportion of genetic association explained by SME should be greater if multiple CpGs are included in mediation analysis. These criteria are helpful to disentangle the causal direction, though its exploratory nature requires caution in interpretation. Altogether, these data support the important role of altered DNA methylation as a mechanism for the influence of these 147 SNPs on gene expression.
Among the eGenes that are regulated by the 147 PrCa risk SNPs in benign tissue, the immune response pathways stand out as the most significantly enriched. This observation corresponds to the risk SNPs in chromosome 6 and various HLA genes located in the region, reiterating the importance of immune responses in the early developmental stage of PrCa. Prostate cancer cells produce a number of tumor associated antigens (TAA) [78,79,80], such as prostate-specific antigen (PSA), prostate acid phosphatase (PAP), and prostate-specific membrane antigen (PSMA). The typically slow growth of prostate tumors allows time for the immune system to mount an anti-tumor response to these antigens. Our eQTL analysis supports the hypothesis that polymorphisms of the HLA alleles are associated with expression levels of various HLA molecules and, likely, the efficiency of immune response to particular TAAs and the risk of PrCa.
While this work presents a comprehensive analysis of eQTLs and meQTLs among 147 SNPs using multiple large genomic datasets, one weakness of our meQTL analysis is that we did not have a large set of normal prostate tissue samples with genome-wide DNA methylation data. This limits our capability to examine the relationship between SNPs, DNA methylation and gene expression in normal prostate. It remains of interest to determine whether the intermediary role of DNA methylation in regulation of gene expression that we observed in tumor samples is consistent in normal prostate samples. Strictly speaking, the tumor-adjacent, histologically benign samples in the Mayo dataset may already have some cancer-related molecular alterations (these benign samples were obtained from patients with PrCa), therefore are not ideal for a tumor-normal comparison study. However, it is difficult to obtain an adequate amount of normal prostate tissue samples through biopsy or donors, e.g., GTEx has a limited number of normal prostate samples. Finally, a limitation for our eQTL analysis is that the FH data were generated using FFPE tissue samples and array-based methods, which may not be ideal for measuring low abundance of mRNA and gene expression. In addition to the difference of clinical characteristics between TCGA and FH data (TCGA has many more high-grade tumors), this factor may also contribute to the differences in eQTL results between FH and TCGA, since the latter used RNA obtained from fresh frozen samples.
In conclusion, we conducted comprehensive eQTL and meQTL analyses for 147 PrCa risk SNPs, in tumors and tumor-adjacent benign samples, and we investigated the role of DNA methylation in eQTL regulation of gene expression. The eQTLs and associated eGenes provide insight into the molecular biology of PrCa, and there is strong evidence that DNA methylation plays an important role in eQTL regulation of gene expression in tumors and in benign samples. These results may guide functional studies that characterize mechanisms of genetic regulation.
Methods
Study populations and sample collection
The Seattle-based Fred Hutchinson (FH) Cancer Research Center PrCa study is composed of European-American male residents of King County, Washington, who were diagnosed with PrCa either in 1993–1996 or in 2002–2005 [81,82]. A subset of patients with clinically localized disease underwent radical prostatectomy as primary treatment, provided a blood sample, and provided consent for access to primary formalin-fixed paraffin-embedded (FFPE) tumor tissue obtained at surgery. Genotype data, gene expression data, and DNA methylation data were generated on this subset of PrCa patients who had blood and tumor tissue available. The details of study and sample collection have been described elsewhere [83]. In summary, the FH study includes 395 cases with both genotype data and at least one of the other data types used in the eQTL or meQTL analysis. The ages at diagnosis ranged from 35–74 years; the distribution of Gleason sum is < = 6 (49.9%), 7 (42.8%) and 8–10 (7.3%). The FH genotype data are part of the recent PRACTICAL consortium analysis which has been deposited to dbGap phs001391.v1.p. The DNA methylation data from FH is accessible at dbGap phs001921.v1.p1. The gene expression data from FH is accessible at GEO GSE141551.
The TCGA study consists of approximately 500 primary PrCa cases diagnosed in 2000–2013, mostly of European ancestry [84]. Fresh frozen prostate tumor samples were obtained by extensive pathologic, analytical, and QC review. Images of frozen tissue were evaluated by multiple expert genitourinary pathologists, and cases were excluded if no tumor cells were identifiable in the sample or if there was evidence of significant RNA degradation. The ages at diagnosis for the TCGA patients ranged from 41–78 years. Gleason scores were < = 6 (9.1%), 7 (49.9%), and 8–10 (41.0%). All TCGA data were downloaded from https://portal.gdc.cancer.gov.
The Mayo study acquired adjacent histologically benign prostate tissue from an archived collection of fresh frozen material obtained from 471 PrCa patients, the majority of whom underwent radical prostatectomy and a few who had cystoprostatectomy at the Mayo Clinic [36]. Hematoxylin and eosin (H&E) slides were prepared from each adjacent benign tissue samples to make sure all were free of prostate adenocarcinoma.
Genotype data collection and processing
For the FH dataset, germline DNA samples (N = 395) were genotyped using two custom Illumina arrays: 1) iCOGS, with 211,000 SNPs; or 2) OncoArray-500K BeadChip with 533,000 SNPs. We applied the following QC on the SNP data: (i) excluded SNPs with call rates <95%; (ii) excluded SNPs that deviated from Hardy-Weinberg Equilibrium (HWE) at P<10−7; (iii) excluded SNPs for which the genotypes were discrepant in more than 2% of duplicate samples. A total of 201,598 SNPs passed the QC criteria for iCOGS data. For OncoArray data, 489,974 SNPs remained for analysis after QC. Germline DNA genotypes for TCGA samples (N = 495) were obtained from the TCGA data portal. Genotypes for 906,000 SNPs were assessed using the Affymetrix SNP 6.0 array. Confidence score was computed at each SNP, ranging from 0 (most confident) to 1 (least Confident). Genotypes with score less than 0.1 are considered to be highly confident (Broad institute, BIRDSUITE software), and 898,000 SNPs were retained in the study. For the Mayo dataset, germline DNA samples (N = 471) were genotyped using the Illumina Infinium 2.5M bead array and genotypic data were downloaded from dbGaP under accession code phs000985.v1.p1. SNPs were excluded if (i) call rate<95%; (ii) HWE<10−5; (iii) MAF<1%. A total of 1,541,380 SNPs were included after QC.
The three datasets utilized different microarray platforms for genotyping and none of them had all 147 PrCa risk variants genotyped. We thus imputed those missing SNPs for each dataset based on the 1000 Genomes Project. Pre-phasing was conducted using SHAPEIT [85]; IMPUTE2 was then used on the phased data to perform imputation [86]. The reference panel used was the 1000 Genomes Phase 3 release, downloaded from the IMPUTE2 website: https://mathgen.stats.ox.ac.uk/impute/1000GP_Phase3.html. After imputation, we used the following criteria to select SNPs from the three datasets: (i) imputation confidence score, INFO ≥ 0.3; and (ii) HWE p-value>1 × 10−6. After imputation, all 147 PrCa risk SNPs passed quality control. The top three principal components (PC) of the genome-wide genotype data were used as adjustment covariates in eQTL and meQTL analyses.
Gene expression data collection and processing
For the FH cohort, the Human HT-12 v4 BeadChip (Illumina) was used for mRNA expression profiling of primary tumor tissues (N = 355). Expression levels for 29,377 transcripts were determined. Among those, 3326 poor quality probes (i.e., probes that matched to repeat sequences, intergenic or intronic regions, or are unlikely to provide specific signal for any transcripts) were removed from the analysis. For those genes with more than one transcript measured (n = 4601), the mean transcript level for each gene was calculated. This resulted in 18,024 genes with transcript data available for eQTL analysis. For the TCGA data, gene expression profiles (N = 492) were obtained from the TCGA data portal. The RNASeq data were generated on the Illumina HiSeq platform. The raw count data for 19,078 genes were converted to Reads Per Kilobase of gene per Million (RPKM) values. For the Mayo study, the RNASeq data were generated using the Illumina HiSeq 2000 platform, and included raw transcript counts for 17,233 genes. These data were downloaded from dbGaP under accession code phs000985.v1.p1. The raw counts data were transformed to RPKM values. In the downloaded Mayo RNA-seq data, RefSeq was originally used as the gene annotation. The gene names were in the Mayo data were converted to the GENCODE annotation, which was used in the TCGA data, in order to make the two datasets comparable in eQTL analysis. For each dataset, gene expression levels for each sample were quantile normalized using the R package preprocessCore [87]. For eQTL-mapping, expression levels of each gene were transformed to the quantiles of the standard normal distribution.
DNA methylation data collection and processing
Tumor DNA was bisulfite converted, and methylome-wide CpG methylation levels were measured using the Infinium Human Methylation450 BeadChip. Background-corrected methylated (M) and unmethylated (U) summary probe intensities were measured for each CpG site, and beta values (M/(M+U)) were used in the meQTL analysis. In the FH study, tumor DNA samples (N = 377) were profiled for 485,577 CpG sites. The following QC steps were applied: (i) The R package Minfi was used to remove probes with a non-detection (p-value) greater than 0.05 and filter out non-CpG-targeting probes (Probe ID prefix = “ch”); and, (ii) cross-hybridizing probes and probes with any SNP within 10 bp of the CpG site or single base extension were removed [88,89,90]. Finally, for each sample 353,245 probes remained for meQTL analysis. The methylation data were normalized using the subset-quantile within array normalization (SWAN) [91], and batch effects were removed using ComBat [92]. For the TCGA study, the tumor methylation data measured on 485,577 CpG sites (N = 495) were obtained from the TCGA data portal. Probes with a non-detection (p-value) greater than 0.05 were removed by TCGA. We further applied the above filter (ii) on these data, and for each sample 396,065 probes remained for meQTL analysis.
Identification of eQTLs
The eQTLs in the Mayo dataset were detected using the linear model, gene expression ~ SNP + top 10 PCs + age + top 15 PEER factors, to regress gene expression of a regulated gene (eGene) on a SNP, adjusting for other covariates. To remove the effect of population structure on gene expression, we used smartpca in the EIGENSOFT program to perform principal component (PC) analysis [93], and selected the top three PCs from genome-wide genotype data as covariates. To remove the hidden batch effects and other potential confounders in the gene expression data, we also used the Probabilistic Estimation of Expression Residuals (PEER) method to select the first 15 PEER factors as covariates [94].
The eQTLs in tumor tissue data were detected using the linear model: gene expression ~ SNP + top 10 PCs + age + top 15 PEER factors + age at diagnosis + pathologic stage + Copy Number Alterations (CNA). For these data, in addition to the above adjustment covariates used for analysis of data from adjacent-benign tissues, we also adjusted for clinical variables such as age at diagnosis and pathologic stage. We also adjusted for copy number alterations (CNA) of the eGene because somatic copy number changes can substantially affect transcript levels in tumors. For TCGA data, the CNA data were obtained from the TCGA data portal. For the FH dataset, 355 cases had both germline genotype and tumor gene expression data. Among these 355 cases, 337 also had tumor DNA methylation data available. We used the R package ChAMP to call CNA on the methylation data [95]; twenty additional adjacent-benign tissue samples were used as the control group to call CNA. The R package qvalue was used to adjust for multiple comparisons [96], and SNPs with a q-value <0.05 were defined as eQTLs. cis-eQTLs were defined if the SNP was within 1 Mb from the eGene region (from the first transcription start site (TSS) to the last transcription end site (TES) of an eGene).
Identification of meQTLs
The meQTLs were detected in the FH and TCGA datasets using the linear model CpG methylation ~ SNP + top 10 PCs of genotype + top 15 PCs of methylation + age at diagnosis + pathologic stage, adjusting for covariates as follows. To remove the effect of population structure on DNA methylation, we used smartpca in the EIGENSOFT program to perform PC analysis [93], and selected the top three PCs of genome-wide genotype data as covariates. To remove the hidden batch effects and other confounders in the tumor methylation data, we picked the first 15 PCs of methylation data as covariates. To remove the potential effects of clinical status on DNA methylation, age at diagnosis and pathologic stage were included as additional covariates. The R package qvalue was used to adjust for multiple comparisons, and SNPs with a q-value <0.05 were defined as meQTLs. cis-meQTLs were defined if the SNP was within 1 Mb from the CpG site. All genomic data were aligned to chromosome positions from the human reference genome GRCh37/hg19.
Analyses to explain the absence of eQTLs in tumors compared benign samples
The R/Bioconductor package edgeR was used for differential gene expression analysis on the 50 TCGA prostate tumors and 50 matched adjacent histologically benign samples [97]. The RNA-seq data contained counts of sequence reads aligned to 60,000 transcripts, of which 52,000 transcripts were included with at least 1 count per million (CPM) in at least two samples. The counts data were normalized using the trimmed mean of M-values (TMM) method, and differential transcripts were using the R/Bioconductor package limma [98].
The TCGA-PRAD level 3 somatic mutation calls for 50 tumor samples were used to compare mutation frequencies in the neighborhood of the two groups of eQTLs. For each eQTL, the number of somatic mutations within 1 Mb distance was counted for each tumor sample and the mutation frequency was computed. The TCGA-PRAD level 3 copy number segmented data for 50 tumor samples were used to compute the fraction of copy number alterations among the tumor samples for the two groups of eGenes. Copy number alterations were defined as a copy number greater than 2.5 or less than 1.5. The TCGA-PRAD level 3 DNA methylation beta values were used to compare the number of DMP and DMR between 50 TCGA tumor samples and 50 TCGA benign samples in the two groups of eGenes. For each eGene we identified the associated probes in the gene, beta values for each probe in the tumor sample group and the benign sample group were compared using the R package geepack [99], and the probe with FWER less than 0.05 was defined as a DMP. The methylation data were also used to compare the percentage of genes within significant meQTL-CpG pairs. For each eGene we identified the paired SNP and associated CpG probes, and checked if there were any SNP-CpG probes included in the meQTL result.
Causal analysis of eQTL, DNA methylation, and gene expression
PrCa risk SNPs that were identified to be both eQTLs and meQTLs were analyzed for causal relationships between associated CpG methylation and gene expression. Mendelian randomization (MR) analysis was conducted by using risk SNPs as instrumental variables, testing causality by regression gene expression on predicted methylation based on genotypes using the two-stage least squares method [54]. This method assumes there is no direct effect from the genotype to gene expression, which can be problematic for this context because there are often multiple adjacent CpGs mediating the genetic effect, any single SNP-CpG-gene expression triplet may present a partial mediation. Moreover, when risk SNPs merely independently affect gene expression and CpG methylation, MR will erroneously detect causality as shown in Fig 5. To effectively distinguish the three possible relationships (Fig 7): namely the mediation relationship of CpG methylation in genetic regulation of gene expression (the SME relationship), risk SNPs independently affecting CpG methylation and gene expression, or there is reverse causation from gene expression to methylation (SEM relationship), a modified CIT mediation test is proposed [55], accounting for the challenge that there are typically multiple CpGs, each of which partially mediates the genetic effect. One advantage of this method over MR is that, with modification, it can test for direction of causality by switching the order of the intermediary and the outcome.
For ease of notation, suppose data contain a genotype (G), two correlated CpG methylation probes (M1 and M2), and a gene transcript (Y). The data generating models are: M1 = α1 G + ε1; M2 = α2G + ε2; Y = γ1M1 + γ2M2 + ε3. In this scenario, M1 and M2 together mediates the genetic effect on Y. If CIT was used to test G→M1→Y, three regression models will be fit: 1) E[Y] = β1G; 2) E[M1] = β2G + β3Y; 3) E[Y] = β4G+β5M1. The four-component test for G→M1→Y includes 1) β1 ≠ 0; 2) β2 ≠ 0; 3) β5 ≠ 0; 4) β4 = 0. If CIT is used to test G→Y→ M1, three regression models will be fit: 1) E[M1] = β1*G; 2) E[Y] = β2*G + β3*M1; 3) E[M1] = β4*G+β5*Y. The four-component test for G→Y→ M1 includes 1) β1* ≠ 0; 2) β2* ≠ 0; 3) β5* ≠ 0; 4) β4* = 0. One can show that in this scenario, CIT will result in significance in both directions, G→M1→Y and G→Y→ M1, a phenomenon observed previously for deciphering the direction of causality between DNA methylation and gene expression [90].
When CIT yielded significant p-values for both the SME and SEM relationships for many of triplets for the eQTL-eGene pair, three criteria are added to distinguish SME from SEM. First, the SME p-values should be generally smaller than the SEM p-values, as the true model should yield a smaller p-value. Second, when there is a single CpG showing significance in testing SME and SEM, the proportion of genetic association with gene expression explained by CpG methylation (for example, β4/ β1 in the models above) should be greater than the genetic association with CpG methylation explained by gene expression, both proportions between 0 and 1 (β4 and β1 having the same sign). The proportion of genetic association explained by a candidate intermediary was computed as the ratio of the genetic association without adjusting for the intermediary (fitting E[Y|G], for example) and the genetic association adjusting for the intermediary (fitting E[Y|M,G], for example). Third, when there are multiple adjacent CpGs showing evidence of mediation, adding multiple CpGs in the mediation model (for example, E[Y] = β4G+β5M+β6M2) should explain a greater proportion of the genetic effect on gene expression than any single CpG. We found in both FH and TCGA data that the third criterion often can effectively distinguish SME and SEM.
Supporting information
S1 Fig [pptx]
All tumor-specific eQTL associations that were identified in one of tumor sets but not in the benign set.
S2 Fig [pptx]
Two examples of loss of or weakened eQTL association in tumor samples when compared to the tumor-adjacent benign samples.
S1 Table [xlsx]
Bioinformatic annotation of 147 prostate cancer risk SNPs.
S2 Table [xlsx]
Results of eQTL and meQTL mapping for 147 prostate cancer risk SNPs among the three datasets (FH, TCGA, Mayo).
S3 Table [xlsx]
Results of Ingenuity pathway analysis for eGenes corresponding to the eQTLs among 147 prostate cancer risk SNPs in the Mayo data.
S4 Table [xlsx]
Results of mediation analyses for triplets of eQTL-CpG methylation-eGenes for prostate cancer risk SNPs which were both eQTL and meQTL (FH and TCGA data).
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