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Conceived and designed the experiments: TL IP MLF. Analyzed the data: TL ND KW IP MLF. Contributed reagents/materials/analysis tools: TL ND IP. Wrote the paper: TL IP MLF.
Cancer is a disease driven by a combination of inherited risk alleles coupled with the acquisition of somatic mutations, including amplification and deletion of genomic DNA. Potential relationships between the inherited and somatic aspects of the disease have only rarely been examined on a genome-wide level. Applying a novel integrative analysis of SNP and copy number measurements, we queried the tumor and normal-tissue genomes of 178 glioblastoma patients from the Cancer Genome Atlas project for preferentially amplified alleles, under the hypothesis that oncogenic germline variants will be selectively amplified in the tumor environment. Selected alleles are revealed by allelic imbalance in amplification across samples. This general approach is based on genetic principles and provides a method for identifying important tumor-related alleles. We find that SNP alleles that are most significantly overrepresented in amplicons tend to occur in genes involved with regulation of kinase and transferase activity, and many of these genes are known contributors to gliomagenesis. The analysis also implicates variants in synapse genes. By incorporating gene expression data, we demonstrate synergy between preferential allelic amplification and expression in DOCK4 and EGFR. Our results support the notion that combining germline and tumor genetic data can identify regions relevant to cancer biology.
Cancer is a disease of two distinct, but related, genomes: the inherited genome and the tumor genome. Despite the fact that the tumor genome arises from the germline, the genomes are typically studied as separate entities. For example, germline genetic studies focus on how inherited variation is related to a particular trait such as disease risk, whereas tumor genetic studies focus on areas of recurrent aberrations such as amplifications to identify genes involved in tumor biology. In this study, we integrated both germline and tumor genetic information to pinpoint areas of the human genome that are likely undergoing selection during the evolution of the tumor. Our results support the notion that combining germline and tumor genetic data can identify regions relevant to cancer biology.
Cancer is a disease of two related, but karyotypically distinct genomes: germline and somatic. Researchers typically focus on identifying genetic alterations by exclusively studying either the germline genome or the somatic genome. Germline genetic variants that play key roles in tumor biology (e.g., risk alleles) have typically been discovered using linkage and, more recently, association studies. On the other hand, somatic genetic elements important for tumor biology, such as amplifications, deletions, and point mutations, are usually identified by patterns of recurrence across tumor samples. Given the kinship between these two genomes, however, studies of cancer biology should be amenable to population genetic analysis, since the tumor cells can be considered descendants of a progenitor cell. In the population of tumor cells, lineages are subject to somatic versions of mutation, drift and selection . We hypothesize that integrating germline allelic (i.e., genotypic) information with somatic amplification events could yield novel insights into the alleles that undergo selection during tumor evolution.
Associations between cancer risk alleles and somatic patterns are beginning to appear in the literature with increasing frequency. Preferential allelic amplification at candidate risk loci has been convincingly demonstrated in several mouse studies ,  as well as in the analysis of the AURKA oncogene in humans , . Additionally, a germline risk allele for colorectal cancer was demonstrated to be preferentially amplified (relative to the wild type allele) in tumors that were heterozygous for this single nucleotide polymorphism (SNP) . More recently, a somatically acquired mutation in JAK2 for myeloproliferative disorders was shown to arise preferentially on a particular haplotypic background –. These targeted studies of specific loci provide compelling evidence for the relationships between the germline and somatic genomes. One of the goals of our study is to perform a genome-wide query for such relationships.
We have developed a battery of statistical methods to query tumor DNA data for preferential allelic amplification . These methods are designed to identify alleles that have likely been positively selected during tumor evolution within areas of copy number gain (Figure 1; Materials and Methods). One of these statistical tests, termed the amplification distortion test (ADT), is closely related to a well-known genetic test of association and linkage, the transmission disequilibrium test (TDT) . Consider an example where N =100 tumors harbor an amplification and are heterozygous at a particular SNP locus (whose alleles are arbitrarily labeled A and B). Under the null hypothesis, on average 50 tumors will amplify one allele, and the other 50 will amplify the alternate allele since tumors typically amplify one of the two parental chromosomes . In this sense, amplification is a somatic analog of Mendelian 5050 transmission in germline genetics. Significant deviations from a 11 ratio (Figure 1B) are inconsistent with this null hypothesis and suggest that the particular allele – or a variant linked to that allele within the same amplified region – is advantageous to the tumor when amplified. Formally, we compare the observed number of germline heterozygotes amplifying the A allele to the Binomial(N, p=0.5) distribution to obtain a two-sided P-value (Materials and Methods and ). Similar to the TDT, the ADT is robust to population stratification because the non-amplified homolog provides a perfectly matched control.
The recent National Cancer Institute-directed initiative, the Cancer Genome Atlas (TCGA; ), provides an ideal resource to test our hypothesis, furnishing SNP array data from multiple platforms across hundreds of glioblastoma multiformae tumors and matched normal samples. Since SNP arrays contain both the allelic and amplification information at hundreds of thousands of loci across the genome, the data are well-suited for our allelic distortion analysis. For each patient in the study, we made use of TCGA-generated SNP genotypes in the germline, as well as amplification status (generated on three separate probe hybridization-based platforms) and allelic amplification status for matched tumor DNA.
TCGA recently published (TCGA, 2008) the first report from a pilot study of over 200 human glioblastoma samples. As part of that study, the tumor DNA was interrogated at some 1.8 million loci using the Affymetrix SNP array 6.0, over 236,000 loci using the Agilent CGH microarray 244A, and at about 550,000 loci using the Illumina HumanHap550 array. We restricted our analysis to the 178 individuals for whom both germline and tumor array data from the Illumina platform were available. From these data, we extracted allelic copy number on a SNP-by-SNP basis; that is, for each individual, we inferred amplification status at each SNP locus, also identifying the amplified alleles in amplicon SNPs. As shown in Figure S1 (and observed in the TCGA manuscript), commonly (>5% of samples) amplified loci are restricted to several discrete – but wide – genomic regions. Such regions have a median length of 166 kb, and regions amplified in at least 15% of samples are usually even longer (median length 382 kb). Such broad regions of recurrent amplification can make it difficult to identify the target of these amplifications.
From a statistical standpoint, although we apply our test statistics across the genome, the ADT is not a genome wide test in the conventional sense because statistical power is expended only in a fraction of the genome. In practice, we only test loci with an amplification frequency sufficiently large to detect allelic selection. The power to detect selected allelic amplification of a SNP depends on its amplification frequency as well as its heterozygosity rate in the sample set . For example, in the ADT, only SNPs with at least nine heterozygote calls in amplified samples have a chance of achieving a nominal two-tailed P-value <0.005. By deciding a priori that P-values above this level will not be considered significant in downstream analysis, we dramatically reduced the candidate loci under interrogation (Figure S2), decreasing the de facto number of SNPs to be tested by 91.9% from 547,458 to 44,132. This represents a far smaller multiple testing burden than in germline genome wide association studies (GWAS). Such reduction in testing burden improves our power to detect true effects.
Figure 2A presents the amplification distortion signals for SNPs tested along the genome. The statistical association for all but the top-scoring SNPs closely follows the distribution expected under the null hypothesis (Figure 2B), attesting to the validity of the assumptions. Although no single SNP achieves genome-wide significance, our results do yield a larger number of SNPs with lower P-values than would be expected by chance. Specifically, given the distribution of amplified heterozygotes in our data, we would expect an average of 114 SNPs to attain a P-value below 0.005 (95% confidence interval 98–132) under the null hypothesis of no random allelic amplification (Materials and Methods). In the actual data, 139 SNPs surpass this threshold (Table S1). This suggests that a subset of the SNPs among these top 139 is likely subject to selective allelic amplification. We checked the level of linkage disequilibrium (LD) these SNPs possess in HapMap CEU data (Table S1); 40 of these 139 SNPs are in strong LD in HapMap (r2≥0.7) with at least one other SNP within this set of 40 (Table S1, Figures S3, S4, S5). Note that our permutation scheme preserves LD structure, so that blocks of SNPs in LD can jointly contribute much of the signal not only in the actual data, but also during each permutation. Therefore, the 139 SNPs are still indeed more than expected by chance.
We should point out that one potential artifact arises from the fact that a germline copy number variant (CNV) gain might appear to be a somatic amplification when compared with the signal intensities from pooled normal samples. However, our methodology guards against this artifact in two ways (Materials and Methods). First, we call amplification in the tumor only if the intensity is greater than that of all normal samples in the study (Materials and Methods). Second, we call the amplified allele only if its allelic intensity is considerably larger in the tumor than in the matched normal. Finally note that, of our top 139 SNPs, only 23 (16.5%) are harbored in gains reported in the Database of Genomic Variants (DGV) (http://projects.tcag.ca/variation/), and of these only 8 are reported in more than three individuals in the database. Therefore, it is quite unlikely that germline CNVs significantly contribute to the ADT signal.
To investigate whether certain classes of genes may be driving our signals, we mapped each of the top 139 SNPs to the nearest gene (within at most 100 kb), which yielded 73 unique genes (Table S1). All but 22 of the 139 SNPs fell within 100 kb of a transcribed region, and 53 of the genes had single SNPs mapping to them. The largest number of significant SNPs mapping to the same gene was seven, all lying within the transcribed region of NSPR1 (see Table S1 for r2 LD values). We performed a gene ontology (GO) analysis  on the gene set to query for enrichment in specific annotations (Materials and Methods). The control set of genes for such analysis deserves special attention in this study, as gene sets may be over represented among our signals simply because they are over represented in amplified regions. To distinguish the signal driven by genes undergoing allelic selection from that driven by more general (non-allelic) amplification, this analysis was conducted by comparing our gene set with genes harboring (or near) SNPs that are recurrently amplified in our data. Thus, any observed enrichment in GO terms is above and beyond that which is due solely to general somatic amplification. This analysis allows us to query for signals from the allele-specific selection, controlling for those due to somatic amplification alone. The results are shown in Table 1 and Figure S6.
Among our five significant (FDR q-value <0.1) GO enrichments is the cellular component term synapse (P=0.0006). Of the 73 genes harboring (or very near) SNPs below the ADT threshold of P-value<0.005, six (CADPS2, CHRM2, CHRNA4, GRM8, MAGI2, and SNAP25) possess this annotation. Notably, the brain-related enrichment is independent of synapse related genes undergoing amplification in brain tumors, since general amplification is controlled for in this analysis. Therefore, the synapse annotation emerged strictly from the ADT selection signal among SNPs already in regions amplified in this brain-tissue tumor. This may be indicative of tumor selection for particular variants in these specific synapse-annotated genes.
Interestingly, the most significantly enriched GO terms (Table 1) were positive regulation of kinase activity (P=9.03×10−5; Benjamini-Hochberg corrected q-value 0.0471) and positive regulation of transferase activity (P=0.000132; Benjamini-Hochberg corrected q-value 0.0471). The six genes in our gene set associated with these GO terms are AGK, DGKB, EGFR, INSR, KIT, and RELN. Each of these genes is the closest to a single significant SNP, with the exceptions of EGFR with two such SNPs, and RELN with three such SNPs (see Table S1 for r2 LD values). Furthermore (Table S1), each harbors one or more of the 139 SNPs within its transcribed region, with the exception of DGKB whose associated SNP is 66 kb downstream. To investigate the relative dependencies between the amplifications of these six genes, we examined the frequencies of their co-amplifications on a sample-by-sample basis. Of the six, four (AGK, DGKB, EGFR, and RELN) are located on chromosome 7. As expected, amplifications of these genes tend to co-occur far more often than would be expected by random assortment (Fisher's exact test P <10−20), largely due to the fact that amplicons often encompass most or all genes on the chromosome. The other two genes are located on chromosomes 4 (KIT) and 19 (INSR). Surprisingly, INSR is co-amplified with chromosome 7 genes in a statistically significant manner (Fisher's exact test P <10−6 for co-amplification with EGFR, odds ratio 14.2). On the other hand, KIT amplification is anti-correlated with that of the genes on chromosome 7 (P=0.05 for anti-correlation with EGFR, odds ratio 0.5). Figure 3 provides an overview of the amplification association structure among these six genes. These correlation patterns may point to interdependent and/or alternative pathways that a tumor engages.
Given the preferential allelic amplification observed in some SNPs, we reasoned that an allele undergoing selection when amplified in a tumor may have an effect on disease risk as a germline predisposition variant. This principle has been previously demonstrated in mice  and in humans –. We therefore compared our list of the top 139 SNPs from our ADT analysis with the 406 SNPs reported in a recent GWAS for glioblastoma . The rationale is that the variant that is selectively amplified in glioblastoma tumors may actually predispose the carrier to the initiation of the tumor, and thereby occur at a higher frequency in cases as compared to controls.
A pair of SNPs, rs4367471 and rs4132013 (r 2=0.78 in CEU HapMap population, Table S1) within a single haplotype block (in the European populations) in an intron of the LHFPL3 gene, appears on both lists. Permutation analysis shows that an overlap of two or more SNPs between lists of these sizes (Materials and Methods) would be expected by chance only 2.1% of the time (P=0.021). This is remarkable since the ADT makes use of no population control genotypes, while the GWAS study does not take tumor DNA into account. For both SNPs, the minor allele is overrepresented on amplified chromosomes (in the present study) and among glioblastoma cases (in the Wrensch et al GWAS). Among 24 amplified heterozygotes for rs4367471 in our study, 20 amplify the minor allele (P=0.0015), while 27 of 32 amplified heterozygotes for rs4132013 amplify the minor allele (P=0.00011). In the GWAS study, the rs4367471 minor allele frequency was 0.28 for glioblastoma cases, as compared to 0.23 for the disease-free controls (P=0.00022). Similarly, the rs4132013 minor allele frequency was 0.24 for cases as compared to 0.19 for controls (P=0.00042). The odds ratios were 1.28 for both SNPs after adjusting for population structure with the Eigenstrat software .
The selective advantage gained by a cell amplifying a specific allele of a gene may be acting through direct changes in a gene product (e.g., a missense SNP) or by regulatory changes that modulate the quantity of gene product. The latter option is a testable hypothesis – it predicts that the amplification of the selected-for variant will be associated with elevated transcript expression levels. To investigate whether any of the detected signals of selected allele-specific amplification associates with expression, we integrated the expression data from the tumor samples with the genotype and amplification status. We considered Affymetrix U133A expression array data from the 154 individuals in our sample set for which the data was available from the TCGA website. Our list of top SNPs includes 65 whose nearest (as measured by base pair distance to transcribed region) gene is represented on the expression array. Of the 65 SNPs, only 28 had at least 5 examples of each SNP allele being amplified among the 154 samples, and were thus available for testing this association. Topping this list of 28 SNPs were rs6959338 and rs13222385, intronic variants in DOCK4 (chr 7q31.1) and EGFR (chr 7p11.2), respectively: rs6959338 shows amplification of the T allele over the C allele in 33 of 41 amplified heterozygotes (P=1.1×10−4); rs13222385 amplifies the G allele over the A allele in 35 of 45 amplified heterozygotes (P=2.5×10−4). Intriguingly, the expression data shows statistically significantly higher expression in samples amplifying the selected-for allele than in those amplifying the other allele (Figure 4) in both DOCK4 (P=0.027) and EGFR (P=0.015). To pursue this idea further, we tested the expression levels of the genes immediately flanking EGFR and DOCK4 for association with amplification of the selected-for alleles. We were interested to discover that LANCL2, a gene 158 kb downstream from EGFR, has statistically significantly higher expression in rs13222385 heterozygotes amplifying the G allele than those amplifying the A allele (P=0.0371). Taken together with the SNP's association with EGFR expression levels, this finding could point to a regulatory element, such as an enhancer for the allele or a linked variant.
We have presented a novel genome wide approach to identify genetic variants that are preferentially selected, via amplification, during tumor evolution. The ADT approach is statistically rigorous and is robust to the confounding effects of population stratification. The non-amplified chromosomal homolog provides the ideal matched control for the amplified homolog, as it comes from the same individual. Although no single SNP individually achieves genome-wide significance under the ADT (likely due to a lack of power owing to limited sample size ), our data does show enrichment in strong ADT signals as compared to chance. Currently, we are performing similar analyses in areas that have undergone copy number loss.
Our integrated analysis of genes harboring (or near) SNPs undergoing apparent allelic selection has revealed intriguing pathways and annotations. As revealed by the GO analysis, many of the variants showing ADT signals with P-values <0.005 are located within genes related to kinase activity. The fact that both the EGFR and KIT kinases reach statistical significance is of particular interest. KIT expression is often observed in gliomas, and imatinib (which is known to inhibit c-Kit) is currently being evaluated in clinical trials –. The correlation/anti-correlation relationships among these implicated genes may highlight glioblastomas that utilize different pathways and may therefore represent distinct subtypes of tumors that may be clinically relevant as has been recently described .
We also observed particular instances of the selectively amplified alleles driving higher expression in DOCK4 and EGFR. DOCK4 was originally isolated in a screen to identify homozygous genomic deletions during tumor progression in a mouse model and is part of a larger family of atypical guanine exchange factor (GEF) for Rho family GTPases . Rho GTPases are highly conserved molecular regulators of cytoskeletal dynamics and influence many cellular processes including cell polarity and migration . Interestingly, it has been previously shown that suppression of DOCK4 RNA reduces dendritic growth and branching in hippocampal neurons, while overexpression enhances these processes . Moreover, increases in Dock180 levels, another Dock family member, enhanced migratory and invasive capacity in vitro, while inhibition of expression significantly reduced glioma cell invasion in vitro . Therefore, we speculate that DOCK4 influences the invasive potential of gliomas and that the DOCK4 alleles may differentially modulate this potential. The role of EGFR in glioma biology is well established  (and references therein). Somatically acquired mutations of EGFR are commonly (~40%–50%) observed in gliomas, and the EGFR pathway is commonly targeted in this disease , –. Our results further substantiate the importance of EGFR and demonstrate that particular alleles play important roles in determining EGFR expression levels. It will be of interest to study if expression differences in this gene lead to amplified or diminished phenotypic consequences. Indeed, a recent article demonstrates that subtle alterations in expression levels can lead to dramatic phenotypic consequences .
The apparent selection of specific inherited alleles when amplified is consistent with several biological interpretations. The data can be considered in the context of Knudson's two-hit hypothesis  in that the associated SNP alleles are inherited variants (or capture variants via linkage disequilibrium) that provide a selective advantage when amplified. Indeed, it has been demonstrated that inherited alleles of a locus (e.g., the Arg72 and Pro72 variants of TP53) can have differential mechanistic effects (e.g., apoptotic potential) . Another explanation is that cis- acting germline determinants influence the acquisition of somatic mutations, which are subsequently acted on by selection. Elegant experiments supporting this hypothesis in mice and humans have recently been published –, . Third, one may hypothesize that a somatic mutation provides a selective advantage only when amplified on a specific haplotypic background, or is selected against if the mutation arises on other allelic backgrounds; that is, only certain alleles will tolerate the somatic mutation.
Since selection implies function, the loci identified in this study are high-priority candidates for further investigation. The results may provide a way to rationally identify subtypes of cancers that are driven by distinct risk loci. If this is the case, then genome wide association studies for cancer risk may benefit from typing matched tumor DNA samples, in addition to germline DNA, and performing an integrative analysis. Alleles that do not affect risk predisposition may still yield important clues with respect to acquired tumor traits, such as angiogenesis, tissue invasiveness, evasion of apoptosis, etc. Functional studies, such as allele specific RNA interference for protein coding regions or somatic cell knock-in of alleles, may shed light on the mechanistic consequences of the alleles.
In summary, we demonstrate that integrating information from germline and tumor genomes can reveal aspects of tumor biology that are not readily identified by studying each genome in isolation.
We obtained glioblastoma array data (GBM Publication Data Freeze) from the ftp site of TCGA. We utilized three different data types – germline genotypes, amplification status, and allelic imbalance – from various hybridization-based platforms, downloaded from the TCGA ftp site. First, germline SNP genotypes (Illumina platform) for all normal samples were obtained. Second, we accessed copy number segmentation data (from Affymetrix SNP array 6.0, Illumina HumanHap550, and Agilent CGH array 244A) for tumor samples, providing genomic regions for each individual that are inferred to have constant copy number along with the estimated “raw” (non-integer) copy number of that segment. Third, we obtained the raw allelic A and B signals for all samples (Illumina BAF measure), tumor and normal. This provides a raw measure of allelic imbalance, commonly termed the “B allele frequency” (BAF), defined as
We also obtained Supplementary Table 7 from the Wrensch et al GWAS , which lists 406 SNPs with p<0.001 for association with high grade glioma comparing cases from San Francisco
Bay Area Adult Glioma Study, 1997–2006 (AGS) and the Cancer Genome Atlas (TCGA) to AGS and Illumina controls (iControls).
For each of the three platforms (Affymetrix, Agilent, and Illumina), we first inferred amplification at all 1.3 million autosomal SNPs represented by the Affymetrix and Illumina arrays combined, as follows. First, for each sample, all SNPs harbored in each genomic segment from the sample's copy number segmentation file (see above) are assigned that segment's raw copy number. A SNP is called amplified by the platform in a tumor sample if its raw copy number in that sample exceeds its raw copy number in all normal samples. This conservative amplification calling procedure accounts for local probe intensity effects, and avoids miscalling germline copy number variants as somatic amplifications. Note that this procedure, while conservative, is designed to include single-copy gains as well as high-level amplification events. Finally, for all downstream analyses, a sample is considered to harbor an amplification at a SNP if it is called amplified by at least two of the three platforms.
For each SNP, we restrict the remainder of our analysis to individuals that are both heterozygous in the germline and amplified in the tumor at the SNP site. For each of these samples, we aim to determine which of the two alleles is amplified. Towards this end, we exploit the BAF measure described above. Since each sample is heterozygous in the germline, we expect the SNP's BAF measure to be near 0.5 in the germline. A tumor BAF larger than 0.5 is indicative of B allele amplification, and a BAF smaller than 0.5 is indicative of A allele amplification. However, bias in A and B intensity measures can result in deviations from these expectations. We therefore rely on the deltaBAF measure, defined as
The expectation here is that A (respectively, B) allele amplification will result in a negative (respectively, positive) deltaBAF value. To avoid erroneous deltaBAF calls due to noisy probe intensities, we only have confidence in allele calls where |deltaBAF| >0.05. That is, for heterozygous (in the germline) samples that are amplified (in the tumor), we call A allele amplification if deltaBAF <−0.05 and B allele amplification if deltaBAF >0.05.
The procedure described above yields sample counts for A amplification and B amplification at each SNP. Let n A and n B, respectively, denote these counts. Under the null hypothesis of random allelic amplification, n A follows a Binomial(n A + n B, 0.5) distribution. In other words, if there is no causal allele or site within an amplified region, the distortion signature of each SNP within the amplified region should conform to the null signature on the binomial distribution. Therefore, a (two-sided) P-value testing preferential allelic amplification may be performed by comparing n A with this distribution in the obvious manner. The chance of a non-causal/non-associated allele within an amplified region being randomly selected enough times to result in a distortion (i.e. false positive) is α, where α represents a chosen level of significance as described in the following section.
Although not a genome-wide association scan, our approaches comprise many tests whose correlations are manifold and complicated. Furthermore, some regions harbor more amplifications than others and therefore have a higher a priori likelihood of displaying allelic distortion even under the null hypothesis. Therefore, analytically determining genome-wide significance from the test statistics is not straightforward. To address this, we developed a permutation procedure that assesses the significance of our results. For each run of the procedure, we first randomly determined – at each sample chromosome pair – whether to swap amplification status from the amplified allele to the non-amplified allele at all amplified (in the tumor) SNPs on the chromosome. This preserves haplotype and amplicon structure while destroying correlation between the two. We then recomputed the test statistics across the genome. In this manner, the amplification status of the samples is preserved, and we are randomly sampling from the null situation of non-preferential (random) amplification. For the ADT test, these simulations produced an average of 114 SNPs (95% confidence interval 98–132) surpassing the 0.005 threshold. For the qq-plot, the qth null P-value quantile was estimated by averaging the qth quantiles of P-values from 1000 permutations. Finally, the significance of the overlap between the ADT SNPs and the Wrensch et al GWAS SNPs was assessed by permuting, 1000 times, and retaining the 139 most significant SNPs for each permutation (since our actual data generated 139 top SNPs). These number of SNPs in each permutation that intersected with the Wrensch list was tallied for each permutation, which yielded the expected distribution expected by chance.
For our GO analyses, we compared the gene list with a “gene universe” comprised of all genes that had any a priori chance of demonstrating preferential allelic amplification, at the P<0.005 nominal level, in our data. For a given gene, this depends upon many factors, including amplification frequency and allele frequencies of nearby array SNPs. We restricted the gene universe to genes that were within 100 kb of a HumanHap550 array SNP that is heterozygous and amplified in at least nine of our samples. This is reasonable, as these are the only genes (by definition) that have an a priori chance of having an associated SNP with ADT P-value below 0.005. This left 2696 genes as a reference set. Using the Ontologizer  software, we assessed our gene lists for enrichment in GO terms, as compared with this reference gene universe, using the Term-For-Term method and Benjamini-Hochberg correction.
For each pair of genes, we constructed a 2×2 table of counts for number of samples in each category of amplification/non-amplification status for each gene. Using this table, we computed the odds ratio estimate for correlation between amplification of the genes, and assessed its significance using Fisher's exact test. For genes X and Y, this corresponds to the ratio of the odds of gene X being amplified in a sample with gene Y amplified to the odds of gene X being amplified in a sample without gene Y amplified.
Expression levels from the Affymetrix 133A array were downloaded from the TCGA website. For each gene/SNP combination, expression differences between samples expressing each of the two alleles were computed using the non-parametric Wilcoxon rank sum test. The test was one-sided, since there was an a priori hypothesis that the preferentially amplified allele would result in a higher expression level.
Proportion of individuals (out of 178) amplified in the tumor, at each Illumina HumanHap550 SNP.
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The number of individuals (out of 178) heterozygous in the germline and amplified in the tumor, at each Illumina HumanHap550 SNP.
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(A) Chromosome 7: Condensed Haploview r2 LD Plot for the three ADT hits (rs10255873, rs10267828, rs1557841) in NXPH1. This condensed plot does not display SNPs in the region that are not ADT hits. The plot indicates that the SNPs are in LD in HapMap CEU data. (B) Chromosome 7: Condensed Haploview r2 LD Plot for the five ADT hits (rs6963353, rs40, rs2107479, rs1467344, rs10950366) in THSD7A. This condensed plot does not display SNPs in the region that are not ADT hits. The plot indicates that the latter two SNPs are in LD in HapMap CEU data. (C) Chromosome 7: Condensed Haploview r2 LD Plot for the seven ADT (rs2530552, rs425990, rs2530571, rs324389, rs10267134, rs10278663, rs17199888) in NPSR1. This condensed plot does not display SNPs in the region that are not ADT hits. The plot indicates that the first three SNPs are in reasonable LD in HapMap CEU data, and the same holds for the latter three SNPs. Any blank red blocks indicate r2 =1.0 (100). (D) Chromosome 7: Condensed Haploview r2 LD Plot for the three ADT hits (rs6965611, rs2464946, rs11238181) in a region with no known gene. This condensed plot does not display SNPs in the region that are not ADT hits. The plot indicates that the first two SNPs exhibit some LD in the HapMap CEU data.
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(A) Chromosome 7: Condensed Haploview r2 LD Plot for the three ADT hits (rs1963647, rs262375, rs264375) in RELN. This condensed plot does not display SNPs in the region that are not ADT hits. The plot indicates that the SNPs display some level of LD in HapMap CEU data. (B) Chromosome 7: Condensed Haploview r2 LD Plot for the four ADT hits (rs10273020, rs4730037, rs4367471, rs4132013) in LHFPL3. This condensed plot does not display SNPs in the region that are not ADT hits. The plot reveals that the first two SNPs are in strong LD in HapMap CEU data, as blank red blocks indicate r2 =1.0 (100). The latter two SNPs also show LD in HapMap CEU data. (C) Chromosome 7: Condensed Haploview r2 LD Plot for the three ADT hits (rs9641684, rs2189601, rs9969220) in CADPS2. This condensed plot does not display SNPs in the region that are not ADT hits. The plot reveals that the first two SNPs are in LD in HapMap CEU data, but they are not in LD with the third SNP.
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(A) Chromosome 20: Condensed Haploview r2 LD Plot for the six ADT hits (rs1923342, rs6131447, rs6109753, rs6105047, rs13433297, rs6074591) proximal to ISM1. This condensed plot does not display SNPs in the region that are not ADT hits. Furthermore, the latter two SNPs (rs13433297, rs6074591) could not be plotted with the former four due to Haploview constraints. In any case, r2 values between the former four and latter two SNPs were negligible in HapMap CEU data. (B) Chromosome 20: Haploview r2 LD Plot for the four ADT hits (rs8120608, rs367114, rs453573, rs6043472) within MACROD2. The SNPs (rs8120608, rs6043472) could not be plotted with the other two due to Haploview constraints. In any case, r2 values between these two SNPs and the two plotted SNPs were negligible. The plot indicates that the two plotted SNPs are in LD in HapMap CEU data, as highlighted by the yellow circle. (C) Chromosome 20: Condensed Haploview r2 LD Plot for the three ADT hits (rs6044739, rs6075193, rs6080665) within PCSK2. This condensed plot does not display SNPs in the region that are not ADT hits. The plot clearly indicates that the first two SNPs are in LD in HapMap CEU data, as any blank red blocks indicate r2 =1.0 (100). The first two are in very weak LD with the third. (D) Chromosome 20: Condensed Haploview r2 LD Plot for the three ADT hits (rs4812744, rs6124601, rs6130470) proximal to TOX2. This condensed plot does not display SNPs in the region that are not ADT hits. The SNP rs4812744 could not be plotted with the other two due to Haploview constraints. The plot clearly indicates that the two plotted SNPs are in LD in HapMap CEU data.
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Gene Ontology acyclic directed graph showing the most enriched terms and their ancestor terms. The significant terms are colored in green, with darker shading indicating greater statistical significance. The arrow colors indicate type of relationship between the GO categories, with black signifying “is a” and green signifying “regulates.”
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Top-scoring SNPs using ADT analysis (p≤0.005) from 178 TCGA samples.
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The authors have declared that no competing interests exist.
This work was supported by grants from the US National Institutes of Health (R01 R01 CA131341 to TL and IP) and (U54 CA121852 to IP). MLF is a Howard Hughes Medical Institute Physician-Scientist Early Career Awardee. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.