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The 12p13.33/RAD52 Locus and Genetic Susceptibility to Squamous Cell Cancers of Upper Aerodigestive Tract

  • Manon Delahaye-Sourdeix,

    Affiliation: Genetic Cancer Susceptibility group (GCS), International Agency for Research on Cancer (IARC), Lyon, France

  • Javier Oliver,

    Affiliation: Genetic Cancer Susceptibility group (GCS), International Agency for Research on Cancer (IARC), Lyon, France

  • Maria N. Timofeeva,

    Affiliations: Genetic Epidemiology group (GEP), International Agency for Research on Cancer (IARC), Lyon, France, Colon Cancer Genetics Group, Institute of Genetics and Molecular Medicine, University of Edinburgh and Medical Research Council (MRC) Human Genetics Unit, Edinburgh, United Kingdom

  • Valérie Gaborieau,

    Affiliation: Genetic Epidemiology group (GEP), International Agency for Research on Cancer (IARC), Lyon, France

  • Mattias Johansson,

    Affiliation: Genetic Epidemiology group (GEP), International Agency for Research on Cancer (IARC), Lyon, France

  • Amélie Chabrier,

    Affiliation: Genetic Cancer Susceptibility group (GCS), International Agency for Research on Cancer (IARC), Lyon, France

  • Magdalena B. Wozniak,

    Affiliation: Genetic Epidemiology group (GEP), International Agency for Research on Cancer (IARC), Lyon, France

  • Darren R. Brenner,

    Affiliation: Genetic Epidemiology group (GEP), International Agency for Research on Cancer (IARC), Lyon, France

  • Maxime P. Vallée,

    Affiliation: Genetic Cancer Susceptibility group (GCS), International Agency for Research on Cancer (IARC), Lyon, France

  • Devasena Anantharaman,

    Affiliation: Genetic Epidemiology group (GEP), International Agency for Research on Cancer (IARC), Lyon, France

  • Pagona Lagiou,

    Affiliation: Department of Hygiene, Epidemiology and Medical Statistics, University of Athens School of Medicine, Athens, Greece

  • Ivana Holcátová,

    Affiliation: Institute of Hygiene and Epidemiology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic

  • Lorenzo Richiardi,

    Affiliation: University of Turin, Department of Medical Sciences, Unit of Cancer Epidemiology, Turin, Italy

  • Kristina Kjaerheim,

    Affiliation: Cancer Registry of Norway, Oslo, Norway

  • Antonio Agudo,

    Affiliation: Catalan Institute of Oncology-ICO, IDIBELL. L'Hospitalet de Llobregat, Barcelona, Spain

  • Xavier Castellsagué,

    Affiliations: Catalan Institute of Oncology-ICO, IDIBELL. L'Hospitalet de Llobregat, Barcelona, Spain, CIBER Epidemiología y Salud Pública (CIBERESP), Madrid, Spain

  • Tatiana V. Macfarlane,

    Affiliation: School of Medicine and Dentistry, University of Aberdeen, Aberdeen, United Kingdom

  • Luigi Barzan,

    Affiliation: General Hospital of Pordenone, Pordenone, Italy

  • Cristina Canova,

    Affiliations: Department of Environmental Medicine and Public Health, University of Padova, Padova, Italy, MRC-HPA Centre for Environment and Health, Respiratory Epidemiology and Public Health, National Heart and Lung Institute, Imperial College, London, United Kingdom

  • Nalin S. Thakker,

    Affiliation: University of Manchester, School of Dentistry, Manchester, United Kingdom

  • David I. Conway,

    Affiliation: University of Glasgow Dental School, Glasgow, Scotland, United Kingdom

  • Ariana Znaor,

    Affiliation: Croatian National Cancer Registry, Croatian National Institute of Public Health, Zagreb, Croatia

  • Claire M. Healy,

    Affiliation: Trinity College School of Dental Science, Dublin, Ireland

  • Wolfgang Ahrens,

    Affiliations: Leibniz Institute for Prevention Research and Epidemiology—BIPS, Bremen, Germany, Faculty of Mathematics and Computer Science, University of Bremen, Bremen, Germany

  • David Zaridze,

    Affiliation: Institute of Carcinogenesis, Cancer Research Centre, Moscow, Russian Federation

  • Neonilia Szeszenia-Dabrowska,

    Affiliation: Department of Epidemiology, Institute of Occupational Medicine, Lodz, Poland

  • Jolanta Lissowska,

    Affiliation: Department of Cancer Epidemiology and Prevention, M. Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland

  • Eleonora Fabianova,

    Affiliation: Regional Authority of Public Health, Banska Bystrica, Slovakia

  • Ioan Nicolae Mates,

    Affiliation: Saint Mary General and Esophageal Surgery Clinic, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania

  • Vladimir Bencko,

    Affiliation: Institute of Hygiene and Epidemiology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic

  • Lenka Foretova,

    Affiliation: Department of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute and Masaryk University, Brno, Czech Republic

  • Vladimir Janout,

    Affiliation: Palacky University, Olomouc, Czech Republic

  • Maria Paula Curado,

    Affiliation: International Prevention Research Institute (IPRI), Ecully, France

  • Sergio Koifman,

    Affiliation: National School of Public Health/FIOCRUZ, Rio de Janeiro, Brazil

  • Ana Menezes,

    Affiliation: Universidade Federal de Pelotas, Pelotas, Brazil

  • Victor Wünsch-Filho,

    Affiliation: Universidade de Sao Paulo, Sao Paulo, Brazil

  • José Eluf-Neto,

    Affiliation: Universidade de Sao Paulo, Sao Paulo, Brazil

  • Paolo Boffetta,

    Affiliation: The Tisch Cancer Institute Mount Sinai School of Medicine, New York, NY, United States of America

  • Leticia Fernández Garrote,

    Affiliation: Institute of Oncology and Radiobiology, Havana, Cuba

  • Diego Serraino,

    Affiliation: Centro di Riferimento Oncologico, IRCSS, Unit of Epidemiology and Biostatistics, Aviano, Italy

  • Marcin Lener,

    Affiliation: Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland

  • Ewa Jaworowska,

    Affiliation: Department of Otolaryngology and Laryngological Oncology, Pomeranian Medical University, Szczecin, Poland

  • Jan Lubiński,

    Affiliation: Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland

  • Stefania Boccia,

    Affiliation: Institute of Public Health, Section of Hygiene, Faculty of Medicine, Università Cattolica del Sacro Cuore, Rome, Italy

  • Thangarajan Rajkumar,

    Affiliation: Dept. of Molecular Oncology, Cancer Institute (WIA), Chennai, Tamil Nadu, India

  • Tanuja A. Samant,

    Affiliation: Cancer Research Institute, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Centre, Navi Mumbai, India

  • Manoj B. Mahimkar,

    Affiliation: Cancer Research Institute, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Centre, Navi Mumbai, India

  • Keitaro Matsuo,

    Affiliation: Department of Health Promotion, Division of Oral Pathology, Kyushu Dental University, Kitakyushu, Japan

  • Silvia Franceschi,

    Affiliation: Infections and Cancer Epidemiology group (ICE), International Agency for Research on Cancer (IARC), Lyon, France

  • Graham Byrnes,

    Affiliation: Biostatistics group (BST), International Agency for Research on Cancer (IARC), Lyon, France

  • Paul Brennan,

    Affiliation: Genetic Epidemiology group (GEP), International Agency for Research on Cancer (IARC), Lyon, France

  •  [ ... ],
  • James D. McKay

    gcs@iarc.fr

    Affiliation: Genetic Cancer Susceptibility group (GCS), International Agency for Research on Cancer (IARC), Lyon, France

  • [ view all ]
  • [ view less ]

The 12p13.33/RAD52 Locus and Genetic Susceptibility to Squamous Cell Cancers of Upper Aerodigestive Tract

  • Manon Delahaye-Sourdeix, 
  • Javier Oliver, 
  • Maria N. Timofeeva, 
  • Valérie Gaborieau, 
  • Mattias Johansson, 
  • Amélie Chabrier, 
  • Magdalena B. Wozniak, 
  • Darren R. Brenner, 
  • Maxime P. Vallée, 
  • Devasena Anantharaman
PLOS
x

Abstract

Genetic variants located within the 12p13.33/RAD52 locus have been associated with lung squamous cell carcinoma (LUSC). Here, within 5,947 UADT cancers and 7,789 controls from 9 different studies, we found rs10849605, a common intronic variant in RAD52, to be also associated with upper aerodigestive tract (UADT) squamous cell carcinoma cases (OR = 1.09, 95% CI: 1.04–1.15, p = 6x10−4). We additionally identified rs10849605 as a RAD52 cis-eQTL inUADT(p = 1x10−3) and LUSC (p = 9x10−4) tumours, with the UADT/LUSC risk allele correlated with increased RAD52 expression levels. The 12p13.33 locus, encompassing rs10849605/RAD52, was identified as a significant somatic focal copy number amplification in UADT(n = 374, q-value = 0.075) and LUSC (n = 464, q-value = 0.007) tumors and correlated with higher RAD52 tumor expression levels (p = 6x10−48 and p = 3x10−29 in UADT and LUSC, respectively). In combination, these results implicate increased RAD52 expression in both genetic susceptibility and tumorigenesis of UADT and LUSC tumors.

Introduction

Upper aerodigestive tract (UADT) cancers, comprising of the oral cavity, larynx and esophagus, are the fourth most common cause of cancer death worldwide [1]. While consumption of tobacco and alcohol are the main UADT cancers risk factors [2], genetic susceptibility has been hypothesized to play a role in the pathogenesis of this disease [3,4].

Exposure to tobacco and alcohol leads to cell damage and DNA alterations that, in the absence of appropriate repair, may cause cell cycle deregulation and cancer development [5,6]. Homologous Recombination (HR) is an important manner by which cells repair DNA lesions [7,8]. The RAD52 gene is involved in the homologous recombination DNA repair process [9] by mediating RAD51, a central HR gene that forms a helical nucleoprotein filament involved in the search for homology and strand pairing [10].

Genome wide association studies (GWAS) have implicated the rs10849605 genetic variant at 12p13.33, the locus that encompasses RAD52 in the human genome, to be associated with a modest, but statistically significant, increased risk of lung cancer [11,12]. It appears most relevant to lung squamous cell carcinoma (LUSC) and small cell lung cancers, but with little evidence within lung adenocarcinomas (LUAD) [11,12]. Although the molecular mechanisms contributing to initiation and progression are still poorly understood, squamous cell carcinomas (SCC) of different anatomical sites share many phenotypic and molecular characteristics with each other [13]. The aim of the present study was to investigate RAD52 in the context of genetic susceptibility to SCC of the UADT, to explore how this association might be mediated and examine the somatic mutation events at the RAD52 12p13.33 locus.

Materials and Methods

Study subjects

A total of 9 case-control studies of UADT cancer participated in our present study totalling 5,947 UADT cancer cases and 7,789 controls. Study designs and population characteristics have been described in more details previously [3,14,15] and are briefly described in Table 1. In most studies, the control subjects were frequency matched to the cases on age, sex, and additional factors (e.g., study site and hospital). Written informed consent was obtained from all study subjects, and the investigations were approved by the institutional review boards at each study center. Analysis was restricted to squamous cell carcinomas.

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Table 1. Demographic characteristics of the cases and controls included in the genetic susceptibility study of RAD52/rs10849605.

http://dx.doi.org/10.1371/journal.pone.0117639.t001

Genotyping

The rs10849605 was genotyped using Illumina bead arrays or TaqMan genotyping (C__1244798_10, Applied Biosystems, Carlsbad, CA) at IARC as described elsewhere [3]. The performance of Taqman assays was validated by re-genotyping samples of known genotype (for example HapMap). The genotype distribution was in accordance with that expected by Hardy-Weinberg equilibrium in each country/study. All subsequent genotyping achieved an internal study duplicate concordance rate of >99%.

The Cancer Genome Atlas data

We accessed to the Head and Neck Squamous Cell Carcinoma (HNSC), Lung Squamous Cell Carcinoma (LUSC) and Lung Adenocarcinoma (LUAD) components of the TCGA data (TCGA Project Number #3230 and #2731). This data is accessible using the dbGAP via the TGCA (https://tcga-data.nci.nih.gov/tcga/). Data were downloaded either from https://cghub.ucsc.edu/ for exome sequencing or directly from https://tcga-data.nci.nih.gov/tcga/ for the RNA sequencing, methylation and genotype data.

Exome sequencing.

We accessed TCGA exome sequencing “level 1” (unprocessed) data for 363 HNSC and 459 LUSC TCGA individuals and completed bioinformatics analysis of their sequence data using Picard, GATK, MuTect and Somatic Indel detector (Methods A in S1 File). Subsequently we used in house bioinformatics pipelines (Methods A in S1 File) to determine the highest quality variant calls. Somatic point mutations were exonic functional variants defined as either truncating, impacting splicing or missense variants predicted as deleterious by SIFT/POLYPHEN2 [16,17].

Copy Number Variation.

Samples were hybridized using the Genome-Wide Human SNP Array 6.0 platform at the Genome Analysis Platform of the Broad Institute. We retrieved level 3 TCGA data of 374 HNSC, 464 LUSC and 476 LUAD individuals containing normalized log2 ratios of the fluorescence intensities between the target sample and a reference sample. We only included in our analysis individuals for whom both tumor and corresponding normal calls were available. For a segment, we considered log2(ratio) < -0.5 to be an indication of a loss, and a log2(ratio) > 0.5 to indicate a gain. Segments with log2(ratio) of between −0.5 and 0.5 were not retained as somatic copy number alterations. Annotation was done adding the genes contained in each of the remaining segments using EnsEMBL databases [18].

RNA sequencing.

RNA sequencing (RNA-seq) TCGA data was retrieved the “level 3” data for 263 HNSC, 223 LUSC and 125 LUAD individuals. Normalization of this data is further detailed within the statistical methods section.

Methylation.

TCGA methylation data was analysed on the Illumina Infinium HumanMethylation 450K BeadChip assay. We accessed TCGA methylation “level 2” data for 263 HNSC, 223 LUSC and 125 LUAD individuals. We estimated the methylated level of each CpG site by calculating the M-value (log2(ratio of methylated and unmethylated probes)) using TCGA level 2 data [19]. Methylation level 2 data is already background-corrected.

rs10849605 TCGA genotypes.

rs10849605 is located inside the 5’ region of RAD52 and was not covered by exome sequencing. Therefore we derived the genotypes for 263 HNSC, 223 LUSC and 125 LUAD individuals using the Affymetrix 6.0 SNP array TCGA data.

Statistical methods

Association analysis.

The association between the variants and UADT cancer risk was estimated by odds ratio (ORs) and 95% confidence intervals (CIs) per allele under the log-additive model and genotype derived from multivariate unconditional logistic regression, with sex and study specific country of origin included in the model as covariates (S1 Table). Heterogeneity of ORs was assessed using the Cochran’s Q test. Statistical analyses were performed using SAS version 9.3 (SAS Institute, Cary, NC, USA).

To control for potential ethnic heterogeneity between cases and controls, we performed a principal components analysis using the EIGENSTRAT package of the EIGENSOFT 5.0 software [20] using 12,898 markers in low linkage disequilibrium [21]. We used the resulting 12 statistically significant eigen vectors (as defined by the Tracy-Widom statistics) in the sensitivity analysis (Table A in S1 File).

eQTL analyses.

The association between rs10849605 germline genotype and RAD52 tumor expression levels (eQTL) was tested on 263 HNSC, 223 LUSC and 125 LUAD using a linear model. It has been repeatedly observed that tumors acquire somatic alterations that can also influence gene expression, particularly copy number changes and DNA methylation [2224]. Therefore we tested the eQTL effect of rs10849605 on RAD52 tumor expression using both adjusted and non-adjusted linear models as described in Table B in S1 File. These statistical analyses were performed using R statistical software (The R Foundation for Statistical Computing, http://www.R-project.org).

In order to control for the impact of population heterogeneity, we inferred population structure of the 263 HNSC, 223 LUSC and 125 LUAD TCGA cases with the Structure software [25] using Hapmap release #23 as the reference population [26] and restricted the eQTL analyses to the 215 HNSC, 192 LUSC and 113 LUAD cases predicted to be of European ancestry (CEU>0.8). On these, we further conducted a principal components analysis similar to the GWAS one. The resulting significant eigen vectors (as defined by Tracy-Widom statistics) were used within the eQTL sensitivity analysis (Table C in S1 File).

Copy number analysis—GISTIC.

We used a publicly available method, called Genomic Identification of Significant Targets in Cancer (GISTIC) [27,28], version 2.0 to find the significantly amplified or deleted regions using TCGA copy number data. The GISTIC algorithm computes p-values for each marker by comparing the score at each locus to a background score distribution generated by random permutation of the marker locations in each sample. Then they correct the p-values for multiple-hypothesis testing using the Benjamini-Hochberg false discovery rate (FDR) method. Therefore the GISTIC scores represent significance levels and are expressed as q-values (significant below 0.25).

RNA sequencing normalization.

Level 3 RNA sequencing tumor data that we accessed from the TCGA was already normalized to the kilobase per million reads (RPKM) standard which corrects for species length and read depth [29], but not for diversity of the RNA population. To control for this we applied TMM (Trimmed Mean of M-values) normalization [30] to the RPKM data. This possibly involves a loss of statistical efficiency relative to applying TMM to raw data, since the precision weighting in TMM will no longer function. However it should not add any bias and the loss of efficiency will be small if the read density is close to uniform. We used implementations in the EdgeR package of BioConductor [31] and the voom function of the Bioconductor limma package [32]. The normal expression data being available only for a few cases, it was not possible to perform any differential expression analysis.

Results

Germline genetic variation rs10849605 and susceptibility to UADT cancers

We genotyped rs10849605 in 5,947 UADT cancer cases and 7,789 control individuals from 9 studies. Frequency of the minor allele of rs10849605 varied somewhat by country, with the risk allele (C) being more prevalent in Europe and Latin America countries compared to Asia (51% and 49% versus 40% respectively).

As observed in squamous cell carcinoma of the lung, the C allele was associated with a modest increase in UADT cancer risk (Fig. 1, p = 6x10−4), with the odds ratio (OR) for having one additional risk allele being 1.09 (95%CI: 1.04–1.15). The association appeared relatively consistent across geographic region (Fig. 1), and did not appear sensitive to cryptic population structure within 1,791 cases and 2,531 controls where genome wide data was available to infer genetic ancestry (Table A in S1 File). The association was also consistent within UADT cancer subsites and consumption of tobacco. However, it was more prominent in those that consumed alcohol compared to non-drinkers (p_het 0.03) (Fig. 1). There was little evidence to suggest this variant altered consumption patterns of tobacco and alcohol (p = 0.53 and p = 0.40, respectively, pack/years and ethanol/day taken as a continuous variable).

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Fig 1. Association between RAD52 SNP rs10849605 and UADT cancer risk.

Squares represent ORs, size of the square represents the inverse of the variance of the log ORs, horizontal lines represent 95% CIs. The solid vertical line indicates OR = 1 and the dashed vertical line the overall OR under the log-additive model. p_het is the p-value for heterogeneity between the different subgroups. I2 is the % of observed variation across subgroups (negative I2 were set to 0).

http://dx.doi.org/10.1371/journal.pone.0117639.g001

Integrated in-silico fine mapping of the 12p13.33 locus

We next undertook in-silico analysis of the rs10849605 variant and the RAD52/12p13.33 locus in the head and neck and lung cancers genomically characterised by the Cancer Genome Atlas (TCGA).

Expression quantitative trait locus (eQTL) of rs10849605 in HNSC and LUSC

rs10849605 is located near the putative promoter 5’ to the RAD52 gene, therefore we hypothesized that this, or a correlated proxy variant, might influence RAD52 gene expression. We performed an expression quantitative trait locus (eQTL) analysis between rs10849605 and RAD52 expression levels in HNSC (n = 263), using data where both RNAseq of the tumors and genotyping had been carried out by TCGA within the same individuals. rs10849605 was significantly associated with RAD52 gene expression levels in HNSC (Fig. 2, n = 263, p = 9x10−4), suggesting that rs10849605 is a cis-eQTL locus for RAD52. The C allele of rs10849605, associated with risk of HNSC, was correlated with increased RAD52 expression levels (Fig. 2). The association was not sensitive either to adjustment for somatic events (copy number or methylation status which may influence eQTL analysis in tumors [22]), HNSC subtype (larynx/hypopharynx, oral cavity, oropharynx) or population structure (Tables B and C in S1 File). A comparable effect was observed in LUSC (Fig. 2, n = 223, p = 8x10−4) but no clear eQTL association was observed in lung adenocarcinoma (LUAD, Fig. 2, n = 125, p = 0.75). While statistically significant, the eQTL for rs10849605 accounted for only a small proportion of the variance (approximately 4%) in RAD52 expression in HNSC and LUSC tumours, an observation in line with the relatively modest genetic risk observed with this variant.

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Fig 2. eQTL analysis.

Boxplots showing the effect of the genotype for the SNP RAD52 rs10849605 on RAD52 tumor expression levels in HNSC, LUSC and LUAD. The risk allele (C) significantly increases RAD52 expression levels (p = 9x10−4 and 8x10−4 respectively) in both squamous cancers but not in lung adenocarcinoma (p = 0.75). In contrast, there was no evidence for association between rs10849605 and expression levels of other genes in the 12p13.33 region (Table D in S1 File).

http://dx.doi.org/10.1371/journal.pone.0117639.g002

Somatic alterations at RAD52/12p13.33 in Head and Neck Squamous Cell Carcinoma (HNSC) and LUSC

Within somatic mutations recalled from paired normal-tumor exome sequencing samples of 305 HNSC and 243 LUSC, RAD52 was rarely mutated somatically (point mutations and insertions deletions), with only 2 HNSC (0.60% of tumors) and one LUSC (0.40% of tumors) patients harbouring a somatic missense variant, and no somatic insertion or deletion observed.

By contrast, we analysed the TCGA somatic copy number variation (CNV) data of 374 HNSC, 464 LUSC and 476 LUAD tumors and found that the 12p13.33 locus was a frequent region of copy number gain in HNSC (7.2% of cases) and LUSC (11.2% of cases). Copy number gain of 12p13.33 was observed in a lower proportion of LUAD tumors (3.9% of cases) (Fig. 3). There was a significant difference in the somatic copy number gain frequencies between SCC and LUAD (p = 3x10−5). Additionally, we used GISTIC2 statistical program to determine the relative importance of the 12p13.33 gain in comparison with the background rate of copy number changes across the genome [27,28] using the TCGA somatic copy number data. The 12p13.33 region was identified by GISTIC2 as a significant focal amplification in HNSC and LUSC (q-value = 0.075 and 0.007, respectively) but not in LUAD (Figure A in S1 File).

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Fig 3. Distribution of individuals by RAD52 expression.

Individuals were ordered by unsupervised clustering based on RAD52 expression levels. Heatmap represents the scaled RPKM normalized values with higher expression levels represented in red and lower expression levels in blue. The individuals carrying a copy number gain (log2(ratio) > 0.5) of RAD52 are highlighted in green (light yellow otherwise). RAD52 gain carriers seem to have the same high expression pattern and cluster together. Particularly in LUAD one of the 3 gain carriers has the highest RAD52 expression level.

http://dx.doi.org/10.1371/journal.pone.0117639.g003

Presence of somatic copy number gain was also correlated with higher RAD52 expression levels in both HNSC and LUSC tumors, (p = 6x10−48 and 3x10−29, respectively) (Fig. 3), with copy number at this locus accounting for a large proportion of the variance in RAD52 tumor expression levels (57% in HNSC and 45% in LUSC). As expected, gene expression levels were correlated with copy number for other genes at 12p13.33 (11 out of 26). However, rs10849605 appeared to influence only RAD52 expression levels (Table D in S1 File).

Discussion

Our study has identified rs10849605 to be associated with UADT cancer (p = 6x10−4). While the modest nature of this association limited our ability to detect inter-substrata heterogeneity, the association was relatively consistent across the diverse etiological settings of Europe, Japan, Latin America and sub-continental Asia (where tobacco chewing is an important UADT cancer risk factor). We note that differing LD patterns, or cryptic population structure where we were unable to control for, could influence these results. Nevertheless, our findings are consistent with the observation that rs10849605 (or variants correlated with it) have also been associated with lung cancer, and particularly lung squamous cell carcinomas. As found in lung cancer [12], the allele C of the susceptibility variant rs10849605 was associated with a modest increased risk of UADT.

rs10849605 is located at chromosome 12p13.33, a locus that contains the RAD52 gene. RAD52 cellular role is DNA double strand break repair via homologous recombination, interacting with multiple DNA repair related genes within this function and therefore a plausible candidate gene to explain this association [33]. Nevertheless, we cannot exclude the possibility of an alternate susceptibility gene to RAD52 due to linkage disequilibrium. We therefore used an in-silico integrative analysis using TCGA expression, genotype and somatic alteration data to fine map this susceptibility locus. 12p13.33 was a region of significant somatic copy number gain in HNSC and LUSC, suggesting that somatic amplification of 12p13.33 is an important molecular event in a subset of tumors. However, the 3MBp amplified region contained multiple genes in addition to RAD52. Importantly, rs10849605 was an eQTL in HNSC and LUSC for RAD52 only, suggesting RAD52 as the most probable candidate driver gene for both the genetic susceptibility and tumorigenesis at this locus. As an eQTL, the rs10849605 UADT and LUSC risk associated allele (allele C) was correlated with increased RAD52 expression levels. That higher RAD52 expression appears involved in both genetic susceptibility and somatic events in UADT and LUSC may indicate that RAD52 activity is enabling tumor cells to have sufficient genome integrity to avoid apoptosis, a trait that may be particularly important within the genotoxic environment created by tobacco smoke and alcohol consumption. Notably, both the eQTL and somatic gains were observed in HNSC and LUSC, but not LUAD, consistent with the lung cancer genetic susceptibility [11,12], reinforcing the importance of this locus in SCC.

A key role of RAD52 is to provide cells with a level of redundancy in DNA repair [34]. RAD52 is therefore particularly important in cells deficient in the BRCA1-PALB2-BRCA2 pathway, providing an alternate mechanism for DNA repair [35,36]. Targeted inhibition of RAD52 in BRCA2 deficient cells results in genomic instability and cell growth inhibition, leading to the suggestion of RAD52 as a potential therapeutic target using synthetic lethality approaches [37]. Our results linking RAD52 higher gene expression to UADT and LUSC, along with our recent observation that a rare truncating BRCA2 genetic variant, rs11571833 (K3326X) is associated with a 2.5 fold risk of squamous cell carcinomas of the lung and UADT [38,39], suggests that such targeted therapy approaches may be worth investigating in UADT and LUSC tumors.

Supporting Information

S1 File. Methods A.

Figure A, Amplification peaks identified across the genome by GISTIC2 in HNSC, LUSC and LUAD. The Gistic-scores are shown on the top and the q-values on the bottom. The significance line is drawn at q-value = 0.25 and the significantly amplified locus are annotated on the right side of each plot. The 12p13.33 amplified region is framed and indicated with an arrow. Table A, Population stratification sensitivity analysis. Model 1 is the original association analysis logistic regression, adjusted for sex and study specific country of origin. Model 2 further adjusts for population stratification including the 12 significant eigen vectors (as defined by Tracy-Widom statistics) as covariates in the logistic regression. Table B, eQTL analyses using adjusted and non-adjusted linear models to measure the impact of the rs10849605 genotype on RAD52 tumor expression levels. The model measures the effect of the protective allele T for rs10849605. Number of individuals taken into account in the model, beta estimates and p-value are given for the three different cancer types and using the following linear models: 1) Non-adjusted, how the genotype influences the gene expression. 2) For HNSC cancer, the subtype (oral cavity, larynx/hypopharynx or oropharynx) is used as the covariate. 3) RAD52 somatic copy number is used as the covariate. 4) Since we are interested here in the influence of somatic determinants on an increase of expression and because methylation is inversely correlated with expression (hypermethylated sites tend to decrease expression when hypomethylated sites induce increase in expression), we selected 8 of the 24 CpG sites for being hypomethylated (as defined by a negative M-value across all individuals in all our 3 different cancer sites). Out of these 8, only cg15612927 was significantly associated with expression of RAD52 in all 3 cancers (p-value < 0.05). Therefore tumor methylation levels of cg15612927 was used as the covariate. 5) The initial model is adjusted for all three somatic alterations (subtype for HNSC, somatic copy number and methylation levels). Table C, eQTL sensitivity analysis. The linear model measures the effect of rs10849605 genotype on RAD52 tumor expression levels. The first line presents the results on all TCGA cases we accessed. The second line restricts the analysis on TCGA cases predicted to be of European origin. The last line show the results of the same linear model but adjusted for the statistically significant eigen vectors, as defined by Tracy-Widom (5 for HNSC and LUSC, 8 for LUAD). Table D, 12p13.33 copy number versus expression and eQTL analysis in HNSC and LUSC. Association analysis between copy number and expression levels for each given gene in the 12p13.33 region (left side of the table, ‘NA’ if no CNV or expression data available). For the significant associations only, we performed an eQTL analysis to check how rs10849605 genotype influences each given gene expression levels (right side of the table). Significant results are highlighted in green (Bonferroni correction for multiple testing).

doi:10.1371/journal.pone.0117639.s001

(DOCX)

S1 Table. Study epidemiological exposures and genetic data.

doi:10.1371/journal.pone.0117639.s002

(XLSX)

Acknowledgments

The authors thank all of the participants who took part in this research and the funders and support and technical staff who made this study possible. We also acknowledge and thank The Cancer Genome Atlas initiative whose data contributed heavily to this study.

Author Contributions

Conceived and designed the experiments: MDS GB P. Brennan JDM. Performed the experiments: MDS JO AC JDM. Analyzed the data: MDS JO MNT VG MJ MBW DB MPV DA GB. Contributed reagents/materials/analysis tools: PL IH LR KK AA XC TVM LB CC NST DIC AZ CMH WA DZ NSD J. Lissowska EF INM VB LF VJ MPC SK AM VWF JEN P. Boffetta LFG DS ML EJ J. Lubiński SB TR TAS MBM KM SF. Wrote the paper: MDS JO MNT MJ JDM. Final manuscript writing: MDS JO MNT VG MJ AC MBW DRB MPV DA PL IH LR KK AA XC TVM LB CC NST DIC AZ CMH WA DZ NSD J. Lissowska EF INM VB LF VJ MPC SK AM VWF JEN P. Boffetta LFG DS ML EJ J. Lubiński SB TR TAS MBM KM SF GB P. Brennan JDM.

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