Candidate locus analysis of the TERT–CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk
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Several studies have reported associations between multiple cancer types and single-nucleotide polymorphisms (SNPs) on chromosome 5p15, which harbours TERT and CLPTM1L, but no such association has been reported with endometrial cancer. To evaluate the role of genetic variants at the TERT–CLPTM1L region in endometrial cancer risk, we carried out comprehensive fine-mapping analyses of genotyped and imputed SNPs using a custom Illumina iSelect array which includes dense SNP coverage of this region. We examined 396 SNPs (113 genotyped, 283 imputed) in 4,401 endometrial cancer cases and 28,758 controls. Single-SNP and forward/backward logistic regression models suggested evidence for three variants independently associated with endometrial cancer risk (P = 4.9 × 10−6 to P = 7.7 × 10−5). Only one falls into a haplotype previously associated with other cancer types (rs7705526, in TERT intron 1), and this SNP has been shown to alter TERT promoter activity. One of the novel associations (rs13174814) maps to a second region in the TERT promoter and the other (rs62329728) is in the promoter region of CLPTM1L; neither are correlated with previously reported cancer-associated SNPs. Using TCGA RNASeq data, we found significantly increased expression of both TERT and CLPTM1L in endometrial cancer tissue compared with normal tissue (TERT P = 1.5 × 10−18, CLPTM1L P = 1.5 × 10−19). Our study thus reports a novel endometrial cancer risk locus and expands the spectrum of cancer types associated with genetic variation at 5p15, further highlighting the importance of this region for cancer susceptibility.
KeywordsEndometrial Cancer Telomere Length Endometrial Cancer Risk Impute SNPs Breast Cancer Association Consortium
Endometrial cancer is the second most commonly diagnosed gynaecologic cancer in the world and accounts for ~5 % of all cancers in women (Kaaks et al. 2002). Worldwide, about 320,000 women are diagnosed with endometrial cancer and approximately 76,000 die of the disease annually (http://globocan.iarc.fr/Default.aspx). Risk factors for this malignancy include long reproductive span (early menarche and/or late menopause), nulliparity, obesity, hormone replacement therapy, tamoxifen, and personal and/or family history of cancer of the endometrium, breast, ovary, or colorectum (Beral et al. 2005; Fisher et al. 2005; Kaaks et al. 2002), suggesting that genetic factors play important roles in the risk of this malignancy (Hemminki et al. 2004). Endometrial cancer can be caused by rare, highly penetrant mutations in DNA repair or replication genes such as MLH1, MSH2, MSH6, PMS2, POLE or POLD1 that result in Lynch Syndrome or in Polymerase Proofreading Associated Polyposis (Briggs and Tomlinson 2013; Fearon 1997; Palles et al. 2013). Genome-wide association studies (GWAS) have also been used to dissect the genetics of endometrial cancer and so far have convincingly identified one associated SNP, rs4430796, on chromosome 17q close to the HNF1B gene (Spurdle et al. 2011; Setiawan et al. 2012; Painter et al. 2014). The rs4430796 G allele is associated with decreased risks of endometrial and prostate cancers, but with an increased risk of type 2 diabetes (Gudmundsson et al. 2007). Candidate gene studies have also identified an association between endometrial cancer and two SNPs in the CYP19A1 gene (Setiawan et al. 2009).
Variants in chromosome 5p15, a region which harbours the TERT and CLPTM1L genes, have been found through GWAS to be associated with the risk of bladder, pancreas, brain, testicular, breast, prostate, skin and lung cancers and glioma (Haiman et al. 2011; Kote-Jarai et al. 2011, 2013; McKay et al. 2008; Petersen et al. 2010; Rafnar et al. 2009; Shete et al. 2009; Stacey et al. 2009; Turnbull et al. 2010; Wang et al. 2014). TERT encodes the catalytic subunit of the telomerase reverse transcriptase enzyme. Activation of TERT transcription occurs in most human cancers where telomerase activity increases to counteract telomere shortening, thereby circumventing the normal limits on cellular proliferation (Kolquist et al. 1998). Little is known about CLPTM1L but recent studies have demonstrated it has an anti-apoptotic role in lung and pancreatic cancer cells (James et al. 2014; Jia et al. 2014; Wang et al. 2014). In recent studies, members of the Collaborative Oncological Gene–environment Study (COGS) used an Illumina iSelect high-density genotyping array (referred to as the “iCOGS” array) and imputation around the TERT–CLPTM1L region to identify several independent variants for breast, ovarian and prostate cancers, and for telomere length in lymphocytes (Bojesen et al. 2013; Kote-Jarai et al. 2013). In the current study, we used the iCOGS array and genotype imputation to investigate whether variants in the TERT–CLPTM1L candidate region are associated with the risk of endometrial cancer in populations of European descent.
Materials and methods
For the iCOGS genotyping, 5,591 women with a confirmed diagnosis of endometrial cancer and European ancestry were recruited via 11 separate studies in Western Europe, North America and Australia, collectively called the Endometrial Cancer Association Consortium (ECAC) (Supplementary Table 1). Germline DNA extracted from blood was used for genotyping.
Healthy female controls with European ancestry and known age at sampling were selected from controls genotyped by the Breast Cancer Association Consortium (BCAC) iCOGS project (Michailidou et al. 2013), or the Ovarian Cancer Association Consortium (OCAC) iCOGS project (Pharoah et al. 2013). We selected the 27,062 BCAC controls from studies in the same countries as the endometrial cancer cases, 744 European-ancestry controls from the Mayo Clinic Ovarian Cancer Case–Control Study (MAY) and 896 controls from the Australian Ovarian Cancer Study (AOCS). In addition, 282 Norwegian blood donor controls with no known history of cancer were genotyped for this study (Supplementary Table 1).
Details of cases and controls are described in the Supplementary Note.
SNP selection and genotyping
Cases and controls were genotyped on a custom Illuminia Infinium iSelect array (“iCOGS”) with 211,155 SNPs, designed by the Collaborative Oncological Gene–environment Study, a collaborative project involving four consortia (Couch et al. 2013; Kote-Jarai et al. 2013; Michailidou et al. 2013; Pharoah et al. 2013). Cases and molecular markers in treatment of endometrial cancer (MoMaTEC) controls were genotyped by the Genome Quebec Innovation Center. BCAC and OCAC control samples were genotyped at four centres. Raw intensity data files for all consortia were sent to the COGS data coordination centre at the University of Cambridge for centralized genotype calling and QC, so that all case and control genotypes were called using the same procedure.
The study presented here relates only to SNPs within a 200 kb region (chr5:1,200,000–1,400,000) including the TERT and CLPTM1L genes. For this region, SNPs were selected for inclusion on the iCOGS array on the basis of published cancer associations and from the March 2010 release of the 1000 Genomes Project (2012). These included all known SNPs with MAF >0.02 in Europeans and r 2 > 0.1 with the then-known cancer-associated SNPs [rs402710 (McKay et al. 2008)] and/or rs3816659 (Shen et al. 2010), plus a tagging set for all known SNPs in the linkage disequilibrium blocks encompassing the genes in the region (SLC6A18, TERT and CLPTM1L). An additional 30 SNPs in TERT were selected through a telomere length candidate gene approach. In total, 134 SNPs were selected, 121 of which were successfully manufactured.
Genotypes were called using Illumina’s proprietary GenCall algorithm, using a cluster file specifically generated for the project using a subset of samples from each genotyping center. SNPs were excluded for call rate <95 % (<99 % for MAF <5 %), MAF <0.1 % or deviations from HWE significant at 10−7, based on a stratified Robinson-Hill test. Samples were excluded for low overall call rate (<95 %), heterozygosity >5 standard deviations from the mean, non-female genotype (XO, XY or XXY), or <85 % estimated European ancestry based on Identical By State scores between study individuals and individuals in HapMap (http://hapmap.ncbi.nlm.nih.gov/) and multidimensional scaling.
For duplicate samples or those identified as close relatives by IBS probabilities >0.85, the sample with the lower call rate was excluded, except for case–control relative pairs for which the case was retained. Among cases, the minimum duplicate concordance rate was 99.96 %. For cases, any 96-well plate containing ≥5 excluded samples was entirely excluded.
For 2,006 cases, we could compare iCOGS genotypes for 40 SNPs with corresponding genotypes from the rapid replication stage of our initial GWAS (Spurdle et al. 2011). Cases with unresolved discrepancies were excluded. After these exclusions, genotypes were available for 113 SNPs in the defined region, in 4,401 cases and 28,758 controls.
We used ImputeV2 (Howie et al. 2009) to obtain in silico genotypes for an additional 1,677 SNPs in this region using two reference panels: the 1000 Genomes Phase 1 (April 2012 release) and an in-house genotyping panel that contained 133 additional SNPs from the October 2010 1000 Genomes Project data release, genotyped in 15,044 samples from the SEARCH and CCHS BCAC studies (Bojesen et al. 2013). After filtering for SNP frequency (MAF ≥0.02; 887 SNPs excluded) and imputation QC (info score ≥0.8; 394 further SNPs excluded), we included 396 SNPs in the association analyses, comprising 113 genotyped and 283 imputed. SNPs with MAF <0.02 were excluded because we would not have statistical power to detect associations with rare SNPs. We used a stringent cutoff for the imputation information score to reduce the chance of spurious associations caused by imputation artefacts. The IMPUTEv2 “leave-out” internal concordance check gave 98.2 % concordance at SNPs with r 2 ≥ 0.8 for SNPs on the 1000 Genomes reference panel but not on the additional in-house panel, and 99.2 % for those SNPs also on the in-house reference panel.
Associations between each SNP and endometrial cancer were estimated using unconditional logistic regression with a per-allele (1df) model, based on the expected genotype dosages for the imputed SNPs. Analyses were adjusted for strata (6 of the 8 strata were defined by country, whilst the large UK dataset was divided into ‘SEARCH’ and ‘other UK’) and for the first 10 principal components of the genomic kinship matrix, based on 37,000 uncorrelated SNPs (r 2 < 0.1), including ~1,000 selected as ancestry informative markers, using an in-house C++ programme incorporating the Intel MKL libraries for eigenvectors (http://ccge.medschl.cam.ac.uk/software/). One principal component was derived specifically for the Leuven (LES/LMBC) studies, for which there was substantial inflation not accounted for by the other principal components.
A ‘global’ test using the admixture maximum likelihood method [AML (Tyrer et al. 2006)] was performed against the null hypothesis that none of the genotyped SNPs within the region are associated with endometrial cancer, with the alternative hypothesis that at least one of the SNPs is associated, based on 10,000 permutations. The test was performed for 55 of the 113 genotyped SNPs, selected such that none of the SNPs had a pairwise r 2 ≥ 0.5 with another SNP in the test.
To determine independently associated SNPs, we used forward stepwise logistic regression based on all SNPs with P < 0.05 in the single-SNP analysis; at each stage, the most significant SNP was potentially eligible for inclusion in the final model if it was significant at P < 0.01 after adjustment for other SNPs. Given the strong prior evidence of cancer associations with this region, this is a candidate gene study, and hence the very stringent significance thresholds required for a GWAS are not applicable here. The 396 SNPs in the analysis can be pairwise-tagged by 68 tagging SNPs at r 2 ≥ 0.5, hence the number of strictly independent tests is closer to 68 than to 396 (and could be considered to be even lower) which would give a Bonferroni-corrected significance threshold of around 0.05/68 = 7.4 × 10−4. An additional logistic regression was performed including all SNPs retained in the step-wise process. Backwards logistic regression was also performed. A secondary analysis was performed in which the most significant independent SNPs from the main analysis were tested for associations specifically with endometrioid and non-endometrioid histology endometrial cancer, and in a case-only comparison of endometrioid and non-endometrioid cases. Pairwise linkage disequilibrium r 2 measures were calculated from the iCOGS samples.
As an alternative to the frequentist stepwise variable selection procedure we also used a Bayesian-inspired penalized maximum likelihood approach which simultaneously analyses all genotyped and imputed SNPs in the region to identify the optimal subset for disease prediction [HyperLasso (Hoggart et al. 2008)]. We used the normal exponential gamma distribution (NEG) shrinkage prior with shape parameter 1.0, as recommended by Vignal et al. (2011). To obtain a SNP-wise type I error of 0.001, we used a penalty (lambda) of 110, estimated based on 100 permutations under the null for different values of lambdas.
The Tagger package (de Bakker et al. 2005) was used to identify independent tagging SNPs for the AML analysis. All analyses were conducted using R, including the GenABEL and SNPMatrix packages (Aulchenko et al. 2007; Clayton and Leung 2007), apart from the HyperLasso analysis (Hoggart et al. 2008) and the AML testing (Tyrer et al. 2006). All statistical tests were 2-sided.
We annotated all SNPs that had moderate to high LD with the three risk alleles identified in our study using Galaxy (Giardine et al. 2005) and the UCSC genome browser. To do so, we followed the annotation scheme described recently by Carvajal-Carmona et al. (2011).
Gene expression analysis
A literature search to identify all published microarray studies investigating endometrial cancer was performed and datasets accessed directly from the author (Moreno-Bueno et al. 2003), publication supplementary data (Risinger et al. 2003; Saidi et al. 2004) or the NCBI Gene Expression Omnibus database [GEO; http://www.ncbi.nlm.nih.gov/geo/; (Day et al. 2011) (GSE17025), (Mhawech-Fauceglia et al. 2010) (GSE23518), (Salvesen et al. 2009) (GSE14860)]. Additional microarray data were downloaded from the Expression Project for Oncology (expO) study via GEO (GSE2190) and TCGA (Kandoth et al. 2013) via the TCGA data portal (http://tcga-data.nci.nih.gov/tcga/tcgaHome2.jsp). TERT expression was interrogated by the platforms used in all eight datasets, whilst CLPTM1L was able to be interrogated by five datasets [(Day et al. 2011; Kandoth et al. 2013; Mhawech-Fauceglia et al. 2010; Salvesen et al. 2009) and expO].
All datasets were log transformed (by taking the logarithmic values of the signals to the base of two) and median centred per array. The change in expression level of TERT and CLPTM1L between non-endometrioid and endometrioid endometrial cancer for each individual study was expressed as an effect size, a unit-free standardized mean difference between groups. Gene expression results were then combined using the t-based modelling approach (Choi et al. 2003) using the meta-package in R. Meta-analysis was performed using a random effects model to account for between-study heterogeneity.
Level 3 (processed) RNASeqV2 normalized expression values for TCGA endometrial cancer samples were downloaded from the TCGA data portal. Differences in TERT and CLPTM1L expression between cancer vs normal tissue and endometrioid vs non-endometrioid endometrial cancer tissue was assessed by Mann–Whitney U test using IBM SPSS Statistics (version 22).
Level 2 (preprocessed) germline GWAS data from endometrial cancer patients was downloaded from the TCGA data portal and QC performed. SNPs were excluded for call rate <95 %, MAF <1 % or deviations from HWE significant at 10−4. Samples were excluded for low overall call rate (<95 %), heterozygosity >3 standard deviations from the mean, inconclusive sex status (X-chromosome homozygosity rate between 0.2 and 0.8), or samples >6 standard deviations from the mean scores for principal component 1 or 2, calculated using CEU individuals in HapMap (http://hapmap.ncbi.nlm.nih.gov/). For duplicate samples or samples identified as close relatives by IBS probabilities >0.85, the sample with the lower call rate was excluded. RNA-Seq Zscores and GISTIC copy number calls for TCGA endometrial cancer samples were obtained via the cBio Portal for Cancer Genomics (http://www.cbioportal.org/public-portal/index.do). There were 192 TCGA samples with both genotype and gene expression data available for analysis. The association of SNPs in the TERT–CLPTM1L gene region (chr5:1,200,000–1,400,000) with TERT and CLPTM1 expression was assessed using PLINK, adjusting for copy number.
We performed high-density genotyping and genotype imputation for variants in the 5p15 TERT–CLPTM1L region to examine genetic associations with endometrial cancer risk. For this purpose, we used a custom-designed Illumina iSelect ~200,000 SNP array (“iCOGS”), which included 118 successfully genotyped SNPs (after standard QC exclusions) spanning a 200 kb region (chr5:1,200,000–1,400,000), to genotype 4,401 endometrial cancer cases from 11 centres participating in the Endometrial Cancer Association Consortium (ECAC) and 28,758 control subjects from the Breast Cancer Association Consortium (BCAC) and the Ovarian Cancer Association Consortium (OCAC). All subjects were of European ancestry (Supplementary Table 1). We then imputed the genotypes of untyped SNPs using 1000 Genomes project data (April 2012 release) as a reference. After excluding SNPs with an imputation information score <0.8 or minor allele frequency <0.02, 113 genotyped and 283 imputed SNPs were included in the analyses. There was no evidence of genomic inflation (λ 1,000 = 1.012, based on 43,233 uncorrelated iCOGS SNPs separate from those presented here).
First, a ‘global’ test using the admixture maximum likelihood method (AML) (Tyrer et al. 2006) against the null hypothesis that none of the genotyped SNPs within the TERT–CLPTM1L region are associated with endometrial cancer provided significant evidence that at least one SNP is associated (P = 0.0001).
The 3 SNPs showing independent associations with endometrial cancer
Position (bld 37)
Frequency of A1
Imputation information score
r 2 with rs7705526
r 2 with rs13174814
OR (95 % CI)
OR (95 % CI)
1.11 (1.06, 1.17)
1.08 (1.02, 1.14)
0.87 (0.82, 0.93)
0.89 (0.84, 0.95)
1.27 (1.14, 1.43)
1.24 (1.11, 1.39)
Whilst the three SNPs in Table 1 were the most significant in the forward logistic regression, each SNP should be considered as a tagging or representative SNP for a set of SNPs, sometimes referred to as an association “peak”. For each of the three SNPs, Supplementary Table 3 lists all other SNPs in the analysis which were in LD (r 2 > 0.2) with that SNP, and which have likelihood ratios of <100:1 relative to the most significant SNP for that set. The SNP sets harbouring rs7705526, rs13174814 and rs62329728 (SNP sets 1, 2 and 3), respectively, contain 12, 4 and 10 distinct SNPs, none of which could be excluded as potentially causative on the basis of statistical analysis. Replacing each of the three imputed SNPs in Table 1 with a genotyped SNP from its own SNP set, each SNP set still showed evidence of association with endometrial cancer in the multi-SNP model, albeit with slightly weaker significance for two of the three sets, indicating that the observed effects are not due to imputation artefacts (Supplementary Table 4).
As an alternative to the frequentist stepwise variable selection procedure, we also used a Bayesian-inspired penalized maximum likelihood approach which simultaneously analyses all genotyped and imputed SNPs in the region to identify the optimal subset for disease prediction [HyperLasso (Hoggart et al. 2008)]. With shrinkage parameters fixed to obtain a Type I Error Rate of 0.001, the four best-fitting models all contained rs13174818 (lead SNP in SNP set 2), and one of rs7705526, rs33961405, rs7725218 or rs7734992, all of which fall within SNP set 1. This differs in some respects from the stepwise regression results, in which rs13174814 and rs62329728 were more significant than rs7705526, and provides further support for a role of SNP set 1 in endometrial cancer.
Of the three SNPs independently associated with endometrial cancer in our study, only one (rs7705526) lies in an LD region previously associated with cancer risk. rs7705526 (OR = 1.11, CI = 1.06–1.17, P = 7.7 × 10−5) is located in the first intron of TERT (chr5:1,285,974, Supplementary Fig. 1a). In the recent COGS study of breast and ovarian cancer risk and telomere length associated with SNPs in the TERT region, rs7705526 was classified as being in what was referred to as “peak 2” (one of two sets of associated SNPs straddling TERT introns 2–4 in that study), and was associated with longer telomeres in blood cells and with increased risks of breast cancer (oestrogen receptor negative and positive subtypes) and ovarian cancer (serous low-malignant potential and serous invasive epithelial) (Bojesen et al. 2013; Pharoah et al. 2013). rs7705526 is in high LD with prostate cancer SNP rs7725218 (r 2 = 0.87) (Kote-Jarai et al. 2013), and also in moderate LD with SNPs in “peak 3” of the COGS study, e.g., r 2 = 0.36 with rs10069690, which is particularly associated with oestrogen receptor negative breast cancer and with both subtypes of ovarian cancer (Supplementary Table 5) (Bojesen et al. 2013; Pharoah et al. 2013). rs7705526 is also in LD with rs7726159 and rs2736100 (r 2 = 0.95 and 0.53, respectively, Supplementary Table 5), which are reported to be associated with multiple cancers including lung, ovarian, testicular, pancreatic and prostate cancers and glioma. Therefore, rs7705526 lies in a complex risk haplotype that is now associated with risks of at least eight different types of cancers.
The two remaining SNP sets identified as independently associated with endometrial cancer risk in our study (represented by rs13174814 and rs62329728) have not, to the best of our knowledge, been previously associated with cancer (Supplementary Table 5), and therefore represent novel risk variants in the region. rs13174814 (OR = 0.87, CI = 0.82–0.93, P = 4.9 × 10−6) maps to the TERT promoter (chr5: 1,299,859 and ~4.7 Kb from the 5′ UTR), a region that has been previously associated with the risk of testicular [rs4635969 (Turnbull et al. 2010)], lung [rs4975616 (Landi et al. 2009; Wang et al. 2008)], prostate [rs7712562, rs2853669, rs2736107 and rs13190087 (Kote-Jarai et al. 2013)] and breast cancers [rs2853669, rs2736108 and rs2736107 (Bojesen et al. 2013)]. However, the previously reported cancer-associated variants show only weak LD with rs13174814 (r 2 < 0.07 for all comparisons) (Supplementary Table 5), suggesting that this SNP represents a novel risk variant for cancer in the promoter region of TERT. The other SNP independently associated with endometrial cancer, rs62329728 (OR = 1.27, CI = 1.14–1.43, P = 2.2 × 10−5), maps to a non-coding region ~12 kb upstream of the 5′ UTR of CLPTM1L (Supplementary Fig. 1c). To the best of our knowledge, rs62329728 is not correlated with any published cancer SNP (r 2 < 0.05), and thus represents a new cancer risk allele in the CLPTM1L region.
rs13174814 and rs62329728 showed similar associations for endometrioid and the more aggressive non-endometrioid histology endometrial cancers (Supplementary Table 6). Although rs7705526 was not significantly associated with non-endometrioid cancers, the number of non-endometrioid cancers (n = 757) was far smaller than the number of endometrioid cancers (n = 3,535), and the case-only endometrioid vs non-endometrioid analyses did not show any significant differences (P > 0.05).
We then assessed association between SNPs in the region and TERT and CLPTM1L expression. Our most strongly associated risk variants were not genotyped by the TCGA genotyping platform (Affymetrix 6.0) and it was not possible to impute these SNPs with a satisfactory degree of accuracy (imputation information scores of 0.41, 0.35 and 0.45 for rs7705526, rs13174814 and rs62329728, respectively) based on this genotyping. Other variants in the region were assessed for association with expression of TERT (Supplementary Table 7) or CLPTM1L (Supplementary Table 8): the best TERT eQTL (P = 0.009) was for rs2853668 (endometrial cancer risk P = 7.2 × 10−4; Supplementary Table 2) located 166 bp from rs13174814 (r 2 = 0.10) in the TERT promoter; the best CLPTM1L eQTL (P = 0.06) was observed for rs2736100 (endometrial cancer risk P = 8.6 × 10−4; Supplementary Table 2), located 542 bp from rs7705526 (r 2 = 0.53). The TCGA genotyping array provided reasonable tags for rs7705526 (best tag rs2736100 with r 2 = 0.53), but not for rs62329728 (best tag rs246992, r 2 = 0.09) or rs1317814 (best tag rs246995, r 2 = 0.13).
Using high-density genotyping, imputation, a ‘global’ likelihood test and multi-SNP logistic regression analyses, we have shown for the first time that genetic variants in the TERT–CLPTM1L region are associated with the risk of endometrial cancer, and provide evidence that this region contains three independent risk SNPs for this cancer. One previous study has reported a nominally significant association between a SNP in the TERT region (rs2736122) and endometrial cancer (reported P = 0.03) (Prescott et al. 2010), but this SNP was not significant in our larger analysis (P = 0.85; Supplementary Table 5), whilst a recent multi-cancer study of nearly 2,000 5p15.33 SNPs did not report an association with endometrial cancer (Wang et al. 2014). Only one of the endometrial cancer risk variants identified in our study (rs7705526) lies in an LD region that has been previously associated with other cancer types.
To date, GWAS for endometrial cancer have convincingly identified evidence for endometrial cancer risk association at the HNF1B locus (Spurdle et al. 2011; Setiawan et al. 2012; Painter et al. 2014), the risk allele of which (rs4430796A) maps to a region that has also been associated with the risk of ovarian and prostate cancers (Gudmundsson et al. 2007; Shen et al. 2013; Thomas et al. 2008). In the candidate study of the 5p15 multi-cancer region presented here, we have identified up to three new independent endometrial cancer risk variants within a locus already associated with multiple cancers, potentially accounting for ~0.5 % of the excess familial relative risk of endometrial cancer. A similar candidate region approach has been used successfully to demonstrate associations between variation at the 8q24 multi-cancer region and thyroid cancer, another understudied malignancy (Jones et al. 2012). We thus propose that future studies on the role of additional multi-cancer regions, such as 1q32/MDM4, 4q24/TET2, 8q24, 10p12/MLT10, 14q24/RAD51B8 or 19q13/MERIT40 (Sakoda et al. 2013), are worthwhile endeavours for cancers that are relatively understudied, including endometrial cancer.
Among the list of 41 TERT SNPs for which we were able to identify a previous report of a significant association with cancer in a European ancestry population (Supplementary Table 5), only those SNPs which are in LD with rs7705526 showed even nominally significant associations with endometrial cancer (with the exceptions of P = 0.032 for rs402710 and P = 0.041 for rs13172201), and none remained significant after conditioning on rs7705526. This suggests that we identified one SNP from a haplotype which is associated with endometrial cancer and also with multiple other types of cancer, and two mutually independent SNPs which are associated with endometrial cancer but do not lie in haplotypes previously reported to be associated with any other type of cancer. However, this does not exclude the possibility that these novel endometrial cancer SNPs are also multi-cancer variants. The 5p15.33 region has complex LD patterns and is poorly tagged by many GWAS genotyping panels. As a comparison, we examined the SNP coverage of this region in a set of 5,180 control subjects genotyped using the Illumina Infinium 1.2M GWAS array as part of the Wellcome Trust Case Control Consortium (2007), for which missing genotypes were imputed using the same method and reference panel as in our main study. Of the 799 SNPs with MAF >0.02, the median imputation information score in the iCOGS set was 0.80 compared with 0.21 in the 1.2M GWAS set, and 87 % of SNPs had an information score of at least 0.4 in the iCOGS set compared to just 26 % of SNPs reaching this threshold in the GWAS set (Supplementary Fig. 2; Supplementary Table 2). These findings emphasize the value of targeted, dense genotyping as a complementary approach to standard GWAS. The imputation information score for rs7705526 (the only one of our associated SNPs previously associated with other cancer types) was 0.55 in the GWAS set, whilst the GWAS information scores for rs13174814 and rs62329728 were just 0.43 and 0.12, respectively. Thus, the use of a deliberately dense panel of local SNPs, such as that used in this study, may reveal associations between the novel endometrial cancer risk SNPs and other cancers.
Fine-mapping genomic regions which potentially contain multiple causal variants is a relatively new area of research, and generally accepted thresholds for claiming the statistical significance of variants do not yet exist. An appropriate threshold for a given region can depend on the number of SNPs tested, the extent of LD in the region, the frequencies of the variants and the prior evidence for association. Some authors have suggested using Bayesian inference as an alternative to frequentist P value-based methods. Here, we performed one such Bayesian-inspired method, the HyperLasso (Hoggart et al. 2008), which also found associations with SNP sets 1 and 2, but reported no further associated SNPs. The results of this alternative method increase our confidence in the associations between endometrial cancer and SNP sets 1 and 2, while direct genotyping of large case–control studies will help towards resolving the disagreement between statistical methods regarding the associations with SNP set 3. The use of imputed genotypes in our analysis allowed us to examine a broader group of SNPs than would have been possible in an analysis restricted to SNPs that had been genotyped. Genotyping cases and controls using the same array, thorough pre-imputation quality control, excluding rarer SNPs and restricting the analysis to SNPs with high imputation information scores (>0.8) should have reduced imputation errors and minimized the chance of false-positive associations (Marchini and Howie 2010). Nevertheless, it will be informative to replicate the analysis using direct genotyping in independent samples.
Two of the endometrial cancer risk SNPs identified in this study are in or near the TERT gene. The risk allele at rs7705526 has been shown to result in increased TERT promoter activity in luciferase reporter assays conducted in ER-negative breast, ER-positive breast and ovarian cancer cell lines (Bojesen et al. 2013), and was reported to be associated with TERT transcript levels in benign prostate tissue (Kote-Jarai et al. 2013). Data from ENCODE show that rs13174814 and another SNP in LD with it, rs13174919, map to a 400 bp region (chr5:1,299,601–1,300,000) identified as an insulator in embryonic stem cells, although an insulator function has yet to be experimentally validated in this or other cell lines. Interestingly, there are also a number of chromatin interactions, indicative of regulatory potential in the region of the most likely causal SNPs for this SNP set in two cancer cell lines (MCF7 and K562) (Supplementary Fig. 1b). Furthermore, our search for functional effects in RegulomeDB (Boyle et al. 2012) and HaploReg (Ward and Kellis 2012) suggests that rs13174814 affects the binding of both RAD21 and CTCF. Previous studies have shown that both RAD21 and CTCF are deregulated or aberrantly expressed in endometrial cancer (Hoivik et al. 2014; Supernat et al. 2012). Interestingly, CTCF appears to be a target for slippage mutations in endometrial cancers with microsatellite instability (Zighelboim et al. 2014).
The third endometrial cancer risk SNP identified in this study is in the upstream/promoter region of CLPTM1L, ~60 kb away from TERT, and which also harbours several cancer risk alleles, mostly for non-hormone-related malignancies such as lung, bladder and pancreatic cancers (Haiman et al. 2011; Kote-Jarai et al. 2011, 2013; McKay et al. 2008; Petersen et al. 2010; Rafnar et al. 2009; Shete et al. 2009; Stacey et al. 2009; Turnbull et al. 2010; Wang et al. 2014). The evidence for an involvement of CLPTM1L in tumorigenesis is, however, more limited. One study has linked CLPTM1L expression with cisplatin resistance in an ovarian cancer cell line (Yamamoto et al. 2001) and more recently, CLPTM1L was shown to promote growth and enhance chromosomal instability in pancreatic cancer cell lines (Jia et al. 2014). Although yet to be functionally characterized, rs62329728 is in LD (r 2 > 0.8) with additional SNPs across the TERT–CLPTM1L region which are located within areas of open chromatin, transcription factor binding or chromatin interactions in multiple ENCODE cell lines including the Ishikawa endometrial cancer cell line (Supplementary Fig. 1c), and hence may have regulatory potential.
Our analysis of microarray datasets suggested differences in CLPTM1L expression between endometrial tumour histological subtypes, and increased expression of both TERT and CLPTM1L between endometrial tumour and normal tissue. Further, a role for TERT is indicated by eQTL analyses, in that endometrial cancer risk-associated SNPs were associated with expression of TERT in endometrial tumour tissue. These results have highlighted a new region of the TERT promoter worthy of functional investigation, and, importantly, implicate CLPTM1L expression in the aetiology of endometrial cancer. As such, these findings will expand biological studies of the TERT/CLPTM1L region in this and other hormone-driven cancers. A possibility that should be examined in future studies is the existence of long-range regulatory elements in this region and their effects on TERT, and whether the prioritized risk-associated variants play a role in CLPTM1L regulation.
In summary, we have used an informed candidate approach to identify a novel endometrial cancer risk locus. Importantly, our study highlights the value of using the information generated by GWAS to guide candidate gene/SNP approaches, particularly for those cancer types that have been relatively understudied using the GWAS approach, such as endometrial cancer. Unlike previous studies in hormone-related malignancies (breast, ovarian and prostate), which only found risk variants in or near TERT, our study found evidence of risk variants in and near TERT and also near CLPTM1L. Future studies should investigate the functional effects of prioritized risk-associated variants on CLPTM1L and/or TERT in endometrial cancer and other cancer models. Furthermore, additional studies, ideally using re-sequencing, should be carried out to uncover possible additional low frequency causal variants.
The authors thank the many individuals who participated in this study and the numerous institutions and their staff who have supported recruitment, detailed in full in the Supplementary Notes. Fine-mapping analysis was supported by NHMRC Project Grant (ID#1031333) to ABS, DFE and AMD. LGC-C receives funding from the University of California Davis, The V Foundation for Cancer Research, and The National Institute On Aging (award number P30AG043097) and The National Cancer Institute (award number K12CA138464) of the National Institutes of Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. ABS is supported by the National Health and Medical Research Council (NHMRC) Fellowship scheme. D. F. E. is a Principal Research Fellow of Cancer Research UK. A. M. D. is supported by the Joseph Mitchell Trust. I. T. is supported by Cancer Research UK and the Oxford Comprehensive Biomedical Research Centre. P. A. F. was partly funded by the Dr. Mildred Scheel Stiftung of the Deutsche Krebshilfe (German Cancer Aid). FA is senior clinical researcher for the Research Fund Flanders (F.W.O.). Funding for the iCOGS infrastructure came from: the European Community’s Seventh Framework Programme under Grant agreement no 223175 (HEALTH-F2-2009-223175) (COGS), Cancer Research UK (C1287/A10118, C1287/A 10710, C12292/A11174, C1281/A12014, C5047/A8384, C5047/A15007, C5047/A10692), the National Institutes of Health (CA128978) and Post-Cancer GWAS initiative (1U19 CA148537, 1U19 CA148065 and 1U19 CA148112—the GAME-ON initiative), the Department of Defence (W81XWH-10-1-0341), the Canadian Institutes of Health Research (CIHR) for the CIHR Team in Familial Risks of Breast Cancer, Komen Foundation for the Cure, the Breast Cancer Research Foundation, and the Ovarian Cancer Research Fund. NCI CA 15083 (Mayo Clinic CCSG) supported the genotyping carried out by the Genotyping Core laboratory. ANECS recruitment was supported by Project Grants from the National Health and Medical Research Council of Australia (ID#339435), The Cancer Council Queensland (ID#4196615) and Cancer Council Tasmania (ID#403031 and ID#457636). SEARCH recruitment was funded by a programme Grant from Cancer Research UK (C490/A10124). Case genotyping was supported by the National Health and Medical Research Council (ID#1031333). NSECG was supported principally by Cancer Research UK and by funds from the Oxford Comprehensive Biomedical Research Centre, with core infrastructure support to the Wellcome Trust Centre for Human Genetics, Oxford provided by Grant 075491/Z/04. The Bavarian Endometrial Cancer Study (BECS) was partly funded by the ELAN fund of the University of Erlangen. The Leuven Endometrium Study (LES) was supported by the Verelst Foundation for endometrial cancer. The Mayo Endometrial Cancer Study (MECS) and Mayo controls (MAY) were supported by Grants from the National Cancer Institute of United States Public Health Service (R01 CA122443, P30 CA15083, P50 CA136393, and GAME-ON the NCI Cancer Post-GWAS Initiative U19 CA148112), the Fred C and Katherine B Andersen Foundation, the Mayo Foundation, and the Ovarian Cancer Research Fund with support of the Smith family, in memory of Kathryn Sladek Smith. MoMaTEC received financial support from a Helse Vest Grant, the University of Bergen, Melzer Foundation, The Norwegian Cancer Society (Harald Andersens legat), The Research Council of Norway and Haukeland University Hospital. The Newcastle Endometrial Cancer Study (NECS) acknowledges contributions from the University of Newcastle, The NBN Children’s Cancer Research Group, Ms Jennie Thomas and the Hunter Medical Research Institute. RENDOCAS was supported through the regional agreement on medical training and clinical research (ALF) between Stockholm County Council and Karolinska Institutet (numbers: 20110222, 20110483, 20110141 and DF 07015), The Swedish Labor Market Insurance (number 100069) and The Swedish Cancer Society (number 11 0439). The Cancer Hormone Replacement Epidemiology in Sweden Study (CAHRES, formerly called The Singapore and Swedish Breast/Endometrial Cancer Study; SASBAC) was supported by funding from the Agency for Science, Technology and Research of Singapore (A*STAR), the US National Institute of Health (NIH) and the Susan G. Komen Breast Cancer Foundation. The Shanghai Endometrial Cancer Genetic Study (SECGS) was supported by Grants from the National Cancer Institute of United States Public Health Service (RO1 CA 092585 and R01 CA90899, R01 CA64277). The Breast Cancer Association Consortium (BCAC) is funded by Cancer Research UK (C1287/A10118, C1287/A12014). The Ovarian Cancer Association Consortium (OCAC) is supported by a grant from the Ovarian Cancer Research Fund thanks to donations by the family and friends of Kathryn Sladek Smith (PPD/RPCI.07), and the UK National Institute for Health Research Biomedical Research Centres at the University of Cambridge. Additional funding for individual control groups is detailed in the Supplementary Text.
Conflict of interest
The authors declare that they have no conflicts of interest.
We declare that all the experiments presented in this manuscript comply with the current laws of the countries in which they were performed. Informed consent was obtained from all individual participants included in the study.
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