Molecular Subtypes in Head and Neck Cancer Exhibit Distinct Patterns of Chromosomal Gain and Loss of Canonical Cancer Genes

Head and neck squamous cell carcinoma (HNSCC) is a frequently fatal heterogeneous disease. Beyond the role of human papilloma virus (HPV), no validated molecular characterization of the disease has been established. Using an integrated genomic analysis and validation methodology we confirm four molecular classes of HNSCC (basal, mesenchymal, atypical, and classical) consistent with signatures established for squamous carcinoma of the lung, including deregulation of the KEAP1/NFE2L2 oxidative stress pathway, differential utilization of the lineage markers SOX2 and TP63, and preference for the oncogenes PIK3CA and EGFR. For potential clinical use the signatures are complimentary to classification by HPV infection status as well as the putative high risk marker CCND1 copy number gain. A molecular etiology for the subtypes is suggested by statistically significant chromosomal gains and losses and differential cell of origin expression patterns. Model systems representative of each of the four subtypes are also presented.


Introduction
Head and neck squamous cell carcinoma (HNSCC) is a heterogeneous disease that represents the seventh most common form of cancer in the United States. Beyond the role of human papilloma virus (HPV), no validated molecular characterization of the disease has been established [1][2][3][4]. To further characterize the diversity of HNSCC as well as other tumors, our group and others have suggested gene expression (GE) subtypes as a means to prioritize the dominant genomic patterns within a specific tumor group [5][6][7][8][9][10][11]. Validated subtypes based primarily on GE profiling of breast cancer, glioblastoma, lung cancer, and others have garnered broad interest [5][6][7][9][10][11]. Preliminary work has suggested that clinically relevant subtypes are also found in head and neck cancer [8], but the findings have not been replicated, no model systems have been proposed, and the etiology of the subtypes is obscure. In other tumor types the validation of molecular signatures has been established by the following approach: (i) the subtypes were shown to be statistically valid, (ii) genomic alterations underlying the subtypes were documented, and (iii) model systems representative of the expression subtypes were identified. The current study was conceived to address each of the points mentioned above. Because the goal of this study was to detect gene expression patterns and underlying genomic events that are present in HNSCC, the study design did not incorporate any molecular subtypes that were defined a priorie.g. subtypes classified by HPV status.

Unsupervised Discovery of HNSCC Expression Subtypes
In order to address the question of whether statistically significant gene expression subtypes can be detected in HNSCC, we performed hierarchical clustering in an unsupervised and unbiased manner using well-established and objective techniques [7]. As in the prior work by Chung et al. [8], we documented the presence of four gene expression subtypes. Gene expression heatmaps ( Figure 1A) and plots produced by ConsensusCluster-Plus [12] ( Figure S1 A -C) do not support the presence of additional statistically significant clusters in this dataset. A representative set of genes known or suspected to be relevant for head and neck cancer is shown in Figure 1B, and test statistics for the association of all genes in the dataset with tumor subtype are provided in Table S1. SigClust [13] analysis showed that the pvalues for all of the pairwise comparisons of the expression subtypes were significant at the.05 level after applying a Bonferroni correction for multiple comparisons ( Figure S1D). We refer to the expression subtypes as basal (BA), mesenchymal (MS), atypical (AT), and classical (CL) based on biological characteristics of genes highly expressed in each subtype.

Clinical Characteristics
The clinical characteristics of the patients included in the current study represent a broad cross section of patients with HNSCC that is highly representative of the population seen in a typical clinical practice (Table 1). There was no correlation of tumor subtype with age, gender, race, alcohol use, pack years, or tumor size. Tumor subtypes were statistically associated with site, although all sites had tumors in each of the expression subtypes, with one exception (hypopharynx showed no BA). Additionally, no site contributed more than 58% of its samples to one expression subtype. No expression subtype was made up of more than 68% of tumors from a single site. Therefore, unlike other molecular markers such as HPV or p16, we conclude that expression subtypes captured a dimension of biology which was not limited to a single anatomic site [14]. There were additional statistically significant associations between tumor subtype and HPV status, treatment, node status, and overall stage. It is notable that more BA trended towards being well differentiated, whereas 13 of 16 poorly differentiated tumors were either MS or CL, although this difference was not statistically significant.

Validation of Subtypes
We then turned our attention to the question of whether the expression subtypes detected in the current dataset corresponded to those previously reported by Chung et al. [8]. Wilkerson et al. [7] presented a method for comparing gene expression patterns found in expression subtypes across multiple studies. We use the same procedure, which is described more fully in the Methods section. Briefly, centroids of expression subtypes measure average gene expression values, and subtypes with concordant expression patterns produce centroids that are more highly correlated than subtypes with discordant expression patterns. A clear correspondence was observed ( Figure 1C), with BA, MS, AT, and CL  demonstrating the same expression patterns as the Chung subtypes 1, 2, 3, and 4, respectively. Having discovered four subtypes using independent and unbiased datasets and methods, we consider these four expression subtypes to be validated.

Distinct Biological Processes and Similarities to Lung Squamous Cell Carcinoma
The expression patterns found in the subtypes suggest the presence of fundamental differences in the underlying biology of the associated tumors (Table S2). Gene expression in BA showed a strong similarity to the signature found in basal cells from the human airway epithelium, including high expression of genes such as COL17A1, which is associated with the extracellular matrix, the growth factor and receptor TGFA and EGFR, and the transcription factor TP63 [14]. Tumors in MS were exemplified by elevated expression of genes associated with the epithelial-to-mesenchymal transition (EMT), including the mesenchymal markers VIM and DES, the transcription factor TWIST1, and the growth factor HGF [15,16]. AT tumors had a strong HPV+ signature, as evidenced by elevated expression of CDKN2A, LIG1, and the transcription factor RPA2 [17]. Tumors in CL, the subtype with the heaviest smoking history, showed high expression of genes associated with exposure to cigarette smoke, including the xenobiotic metabolism genes AKR1C1/3 and GPX2 [7,18,19] and the transcription factor NFE2L2 [10].
Squamous cell carcinomas from different sites in the body share a number of molecular characteristics -e.g. loss of chromosome 3p and gain of chromosome 3q [20,21] -so we hypothesized that a correspondence between our expression subtypes and recently reported lung squamous cell carcinoma (LUSC) expression subtypes [7] would be observed. To investigate a broader phenotype of squamous cell carcinomas of the upper aerodigestive tract, we extended the centroid predictor methodology and evaluated the correspondence of centroids from LUSC and HNSCC ( Figure 1D). Remarkably, a clear pattern of correlation was observed in which the BA, MS, and CL subtypes of HNSCC corresponded to the LUSC basal, secretory, and classical subtypes, respectively, of Wilkerson et al. [7]. Examination of the TCGA LUSC data [10] provided additional compelling evidence of the underlying connections between the expression subtypes at the two tumor sites ( Figure S2). The correspondence between the basal subtypes is notable because Wilkerson et al. [7] described time course experiments involving cultured human bronchial epithelial cells in which gene expression patterns at early time points showed a strong resemblance to those seen in the basal subtype of LUSC. Similarly, as shown in Table S3, we observed that the basal subtype of HNSCC is most similar to the day 3 time point in the time course data from the air liquid interface (ALI) model [22].

DNA Copy Analysis by Subtype
We then turned our attention to the genomic alterations of HNSCC as measured by copy number (CN) arrays. First we confirmed many regions previously reported as altered in HNSCC, including gain of chromosomes 3q, 7p, and 11q (statistically significant gains are seen in both 11q13 and 11q22) and loss of chromosomes 3p, 9p, and 14q (Table S4 ). As has been seen in other tumors [11], there are both concordant and discordant patterns of copy number alteration in key regions of the genome as a function of tumor subtype ( Figure 2, Table S5 ). For example, gains of 3q vary by expression subtype (p = .01), whereas no significant CN differences between the subtypes were detected in 11q13, which contains CCND1 (p = 1). The canonical HNSCC 7p gain occurred in a region containing EGFR, but these alterations were found in BA, MS, and CL, not AT (p = .01). CN values in 3p were not significantly different across the subtypes (p = .47). Losses of the 9p region that contains CDKN2A were found in BA and CL only, and the CN differences were significant (p = .01). Focal CN loss was found in 14q32 for MS, CL, and is particularly pronounced in AT, but although this did not not reach statistical significance. This region contains miR203, which is notable because it targets DNp63 [23], one of six protein products of TP63. Chromosomal instability also varied considerably by subtype (p = 2.2e-4), as seen in Figure S3.

Copy Number Changes and Differential Expression of Genes in Chromosome 3q by Expression Subtype
One of the quintessential genomic alterations associated with squamous cell carcinomas is gain of 3q [20,21], and in the previous section we noted that the CN values in this region varied by expression subtype. Interestingly, there was a distinct differential proportional usage of the three genes typically discussed as the targets of the amplicon: TP63, PIK3CA, and SOX2 ( Figure 3). The CL and AT subtypes demonstrated proportionally higher expression of SOX2 relative to MS and BA, which in fact appeared to express less SOX2 than normal tonsil controls. By contrast, the BA subtype expressed dramatically higher levels of TP63 than any other group. Similarly, although the MS subtype exhibited copy number gains in 3q, none of the putative target genes appeared to be expressed at levels higher than normal tonsil. Kruskal-Wallis tests showed that the expression of each of TP63, PIK3CA, and SOX2 was associated with expression subtype after a Bonferroni adjustment for multiple testing (Table S6 ). This observation raises the possibility that the heterogeneity of HNSCC might in part be explained by differential usage of the transcription factors (SOX2 and TP63) and oncogene (PIK3CA) in the 3q amplicon, which is more complex than has been previously reported [24]. It also suggests that differential usage of transcription factors and oncogenes, promoted in part by distinct copy number alterations, may contribute to the gene expression signatures that define the expression subtypes.

Copy Number Events Involving Canonical Cancer Genes
Earlier we noted that the copy number values in gain and loss regions were associated with expression subtype. Now we describe similar findings that were obtained when gene-specific copy number values for genes known to play a role in HNSCC -CCND1, CDKN2A, and EGFR -were considered, not the broader regions discussed above. In the above discussion we stated that gains of 11q13 were not significantly different across the subtypes, and Table 2 shows that similar results were found when attention was restricted to gains of CCND1. In contrast, the frequency of EGFR gains ranged from 0% in AT to 31% in CL (p = .069), while the frequency of CDKN2A losses varied between 10% in MS to 63% in CL (p = .004). Both of these findings are concordant with the findings in the broader regions of 7p and 9p, respectively, described above.
Past studies have detected associations between distinct genomic events, and these findings provided insight into either the underlying biology or the clinical management of cancer patients [25,26]. In HNSCC, simultaneous CCND1 gains and CDKN2A losses have been studied by Okami et al. [27] and Namazie et al. [28], with Namazie et al. detecting an association between these genomic events. We found that CCND1 CN gains were associated with CDNK2A losses across all subtypes (Table S7), and that the joint event was associated with the expression subtypes (Table 2), thereby confirming and extending the results of Namazie et al.

Clinical Outcomes by Expression Subtype and Focal Genomic Alterations
Having parsed the set of nearly 140 HNSCC tumors into expression subtypes, and in light of known risk factors such as HPV, smoking, and alcohol use, we considered whether additional stratification for patient outcomes could be suggested. We first investigated whether the survival advantage reported by Chung et al. for ''subtype 10 could be reproduced in the current cohort. We were unable to confirm this result, and in the current study there was no association between recurrence-free survival and tumor subtype, either overall ( Figure 4A) or when we restrict to late stage patients (not shown). These differences may be explained by the clinical heterogeneity of the disease combined with the fact that tumor site distributions in the two studies are markedly different.
In order to clarify whether known or suspected confounders might have affected our ability to detect subtype-specific differences in patient outcome, we evaluated the impact of HPV status on overall survival. We observed a relatively large but imprecise effect due to the overall small number of HPV+ patients ( Figure 4B). We therefore considered it reasonable to re-evaluate the cohort with HPV+ patients excluded. Exclusion of HPV+ patients revealed that the AT subgroup demonstrated a particularly unfavorable outcome ( Figure 4C), and this difference was statistically significant when compared to all other subtypes combined ( Figure 4D). We then accessed an independent set of 122 tissue microarray (TMA) samples in an effort to validate this finding. Because array-based GE and immunohistochemistry (IHC) staining values are not comparable, it was not feasible to  predict the tumor subtype of each TMA sample. Instead we used low EGFR and high p16 staining as a proxy for AT status. The difference in survival times was not statistically significant, but we obtained results similar to those described above ( Figure S4).
We also investigated whether any focal copy number events were associated with clinical outcome. Previous studies have detected a correlation between CCND1 gains and decreased recurrence-free survival times in HNSCC [29]. We obtained similar findings when we examined the CN values for all tumor samples ( Figure S5), although our results are marginally significant (p = .07). Remarkably few AT subjects exhibited CCND1 gains (Table 2), and this suggests the presence of two largely distinct groups of patients with poor clinical outcomes: those with CCND1 gains and those that are HPV2 and AT. Figure S6 supports this conclusion.

Expression Subtypes in Model Systems
The Cancer Cell Line Encyclopedia [30] contains genomic data from over 900 human cancer cell lines, including both GE and CN data from 19 esophageal and 18 upper aerodigestive tract cell lines. We applied our centroid predictor to the GE data from these cell lines and found that all four expression subtypes were present (Table S8). These findings are particularly compelling in light of the clinical relevance of the expression subtypes because they provide the basis for future studies involving model systems. Figure  S7 provides examples to illustrate that subtype-specific CN events are also seen in the cell lines.

Discussion
Our primary result was the detection of four gene expression subtypes in HNSCC -basal, mesenchymal, atypical, and classical. We also showed that these subtypes have biological and clinical relevance, and therefore they provide a useful and informative mechanism of classifying HNSCC tumors that complements existing methods based on histology and tumor site. Analysis of publicly available expression datasets revealed that these subtypes are reproducible in HNSCC [8] and are remarkably similar to those found in LUSC [7,10]. Although gene expression patterns for the secretory LUSC subtype are similar to those seen in the mesenchymal subtype of HNSCC, we favor an alternate nomenclature. Data confirming the glandular origin of HNSCC is less compelling compared to that for the lung, and evidence of a mesenchymal signature is abundant [7]. While it would be possible to use the existing data to produce a gene predictor for HPV status, we did not attempt to do this because results of this nature were presented by Martinez et al. [31]. Regions of recurrent DNA copy number gain and loss were detected, some of which contain known oncogenes and tumor suppressors. The copy number values in certain aberrant regions were associated with tumor subtype, which suggests that copy number events may contribute to the development of expression subtypes. All of the expression subtypes were detected in HNSCC cell lines, a finding that provides the basis for future studies.
We now briefly discuss the definitions of the expression subtypes. Basal and classical were chosen because the expression patterns in these subtypes showed strong similarities to the basal and classical subtypes of LUSC. Wilkerson et al. compared the expression patterns in the LUSC subtypes to time course data from developing human bronchial epithelial cells, and they found that the basal subtype had similar expression patterns to those seen at early time points when basal cells are most common. Similarly, as shown in Table S2, we observed that the basal subtype of HNSCC is most similar to the day 3 time point in the time course data from the ALI model [22]. The classical subtype exhibits canonical genomic alterations associated with squamous cell carcinoma -e.g. deletion of 3p and 9p, amplification of 3q, and focal amplification of both EGFR and CCND1. Mesenchymal was selected based on pathway analysis indicative of an epithelial to mesenchymal transition. Finally, atypical was chosen because of the lack of either EGFR amplification or deletion of 9p.
The differences in the expression patterns found in the subtypes are clinically relevant. TP63 produces six distinct proteins, and DNp63 is the most abundant isoform in HNSCC [32]. Yang et al. [33] show that DNp63 promotes cell proliferation. Chatterjee et al. [32] noted that exposure to cisplatin led to decreased levels of DNp63, so this treatment may be particularly effective for patients in BA. Barbieri et al. [34] showed that loss of TP63 in HNSCC cell lines led to the acquisition of a mesenchymal phenotype, which is compelling in light of the low expression levels of TP63 seen in MS. Martin and Cano [35] indicated that elevated expression of TWIST1 or BMI1 in HNSCC cell lines could increase the likelihood of invasiveness and migration. Because MS tumors exhibited an EMT phenotype and increased expression of both TWIST1 and BMI1, these subjects may be more likely to develop distant metastases. The fact that EGFR is overexpressed in the vast majority of HNSCC tumors [36] makes EGFR inhibitors an attractive treatment option for this disease. However, these therapies are less likely to be effective in AT tumors because EGFR expression was lower than in the other expression subtypes. SOX2 and ALDH1 were highly expressed in AT and CL, and both of these genes are putative cancer stem cell markers because of their contributions to self-renewal and a pleuripotent phenotype [37,38]. The protein product of PIK3CA is p110a, which phosphorylates AKT. Activated AKT contributes to the survival of tumor cells, and thus oncogenic transformation [39]. West et al. [40] showed that exposing normal lung epithelial cells to nicotine facilitates activation of AKT by making it dependent on PI3K alone. This observation, combined with the high levels of smoking seen in CL, suggests that PI3 kinase inhibitors provide an attractive treatment option for CL tumors. There were several limitations to this study. First, we did not have GE, CN, and clinical data for all study subjects, which limited our ability to jointly analyze these variables. In addition, although the subtype labels were objectively defined by a clustering algorithm and the gene expression patterns were independently validated, the clinical associations were not. Copy number arrays were generated for all samples with sufficient quality and quantity of DNA. Unfortunately, over 20% of the arrays failed to meet standardized quality metrics. Also, it was not clear which isoform(s) of TP63 were assayed by our gene expression arrays, and unfortunately the role that TP63 plays in the basal subtype cannot be fully appreciated without knowledge of these isoforms. Because the HPV+ samples were removed when conducting our secondary survival analysis, these results should be viewed as exploratory and thus must be independently validated. Finally, the HPV status of all patients was not available.
In conclusion, we confirmed four molecular classes of HNSCC (basal, mesenchymal, atypical, and classical), consistent with signatures established for squamous carcinoma of the lung. Using an integrated genomic analysis and validation methodology, we documented subtypes identified by canonical tumor suppressor genes and oncogenes, including deregulation of the KEAP1/ NFE2L2 oxidative stress pathway, differential utilization of the lineage markers SOX2 and TP63, and preference for the oncogenes PIK3CA and EGFR. For potential clinical use, the signatures are complimentary to classification by HPV infection status as well as the putative high risk marker CCND1 copy number gain. A molecular etiology for the subtypes is suggested by statistically significant chromosomal gains and losses and differ-

Tumor Collection and Genetic Assays
After receiving written informed consent, frozen, surgically extracted, macrodissected head and neck tumors were collected at the University of North Carolina under Institutional Review Board protocol #01-1283. Tumor RNA was extracted and mRNA expression was assayed using Agilent 44K microarrays. Tumor DNA was extracted and DNA copy number was assayed using Affymetrix GenomeWide SNP 6.0 chips. A summary of all genetic data used in this study can be found in Table S9.

mRNA Expression Analysis
Quality control procedures were applied to microarray probelevel intensity files. A total of 138 tumor arrays remained after removing low-quality arrays, duplicate arrays, and arrays from non-HNSCC samples. The normexp background correction and loess normalization procedures [41] were applied to the probelevel data. After log 2 transformation, probes were matched to a common gene database to produce expression values for 15597 genes.

Unsupervised Expression Subtype Discovery
The procedure described here is similar to that which appeared in Wilkerson et al. [7]. After expression values were gene median centered, gene variability was computed using the median absolution deviation. The 2500 most variable genes were selected. ConsensusClusterPlus [12] was used to perform unsupervised clustering for these genes in the 138 arrays. This procedure was performed with 1000 randomly selected sets of microarray samples using a sampling proportion of 80% and a distance metric equal to one minus the Pearson correlation coefficient.

Statistical Significance of Gene Expression Patterns in Expression Subtypes
To confirm the statistical significance of four clusters, SigClust [13] was applied using the set of the 2500 most variable genes described above. All pairwise comparisons of the subtypes were examined using 1000 simulated samples and the original covariance estimation method.

Differentially Expressed Genes and Metabolic Pathways
Differentially expressed genes were detected with the R package samr [42] using a median FDR threshold of.01. For each of the UNC subtypes we compared the gene expression values in the subtype to all other subtypes combined. DAVID [43] was then used to find KEGG pathways that showed enrichment for the highly expressed genes in each subtype. In addition, differentially expressed genes with known functional categories, e.g. transcription factors, were found by comparing the subtype-specific gene lists to known gene ontology categories [44].

Published Expression Data
The microarray probe-level intensity files produced by Chung et al. [8] were subjected to background correction, normalization, and gene-level summarization procedures similar to those described above. This produced gene expression values for 60 subjects and 8224 genes. The subtype labels for these 60 arrays that appeared in [8] are referred to as Chung subtypes 1, 2, 3, and 4.
Summary RPKM values for 20,502 genes and 178 subjects were obtained based on the RNASeq data presented in [10]. The RPKM values were log 2 transformed, and any gene that contained at least one missing value was removed from the analysis. This produced gene expression value for 15,314 genes.

Validation of Expression Subtypes
Consensus clustering assigns a subtype label to every array. As a result, some arrays may not be representative of their subtype. Using silhouette widths [45], we identified a set of 125 ''core'' samples whose expression patterns were more similar to those of members of their own subtype than other subtypes. ClaNC [46], a classification method based on nearest centroids, was then applied to the UNC expression data from the core samples in an effort to create a set of classifier genes whose expression signature could be used to classify new samples. Minimizing the crossvalidation error rate produced a list of 840 classifier genes (210 genes per subtype).
We identified the classifier genes whose expression values are also present in the Chung expression dataset, and then restricted the UNC and Chung expression datasets to these genes. After gene median centering each dataset separately, we found the centroid for each of the UNC and Chung subtypes by computing the median expression value for each gene over all arrays having the appropriate subtype label. As in [7], the distances between the UNC and Chung centroids were computed using a distance metric equal to one minus the Pearson correlation coefficient. This validation process was repeated using the LUSC data of Wilkerson et al. [7]. The RNASeq data from [10] was handled similarly with the following differences: (i) gene expression values from the UNC and log 2 (RPKM) values from the TCGA datasets were separately median centered and standardized by gene, (ii) predicted class labels were found, but class centroids were not computed.

DNA Copy Number Analysis
CEL files were subjected to quality control procedures using the Affymetrix Genotyping Console, and arrays that produced contrast QC measurements above the default threshold of.4 were removed from subsequent analyses. The intensity values in the CEL files were then converted to log 2 copy number values using the R package aroma [47] and a pooled collection of normal samples. A total of 107 arrays remained after manually reviewing the genome-wide copy number profiles, 84 of which have expression subtype labels. Missing values were imputed using the non-missing value from the closest probe. Segmentation was performed using DNAcopy [48].
Recurrent copy number gains and losses were detected with DiNAMIC [49] after smoothing and median centering the copy number profiles, as was done in [11]. DiNAMIC p-values were computed using 250 cyclic shifts, and gains and losses were classified as statistically significant if resulting p-values were less than.05. Regions harboring recurrent CN gains and losses were found using the bootstrap confidence interval procedure at level.95 with 500 bootstrap samples.
Associations between expression subtype and the five most significant gain and loss events were assessed as in [11]. First, for each subject the mean CN value over the corresponding confidence interval was computed. This was done with the smoothed and median centered CN values that were used to compute the confidence intervals, as described above. Then Kruskal-Wallis tests were applied to assess the association between each subject's mean CN value and the expression subtype labels.

Copy Number Gains and Losses of Canonical Cancer Genes
The gene-specific copy number was determined by computing the mean of all segmented copy number values at probes lying within or immediately adjacent to the gene. For each subject we classified a gene as having a copy number gain (loss) if the genespecific copy number was above.35 (below 2.35), which is approximately two standard deviations above (below) the mean of all segmented copy number values.  [50] was used to perform all survival analyses, and all p-values were computed using the log rank test. Recurrence-free survival (RFS) time was defined to be the time in months from tumor biopsy to death, recurrence, or loss to follow-up. Complete clinical data for all subjects, including RFS time, is presented in Table S10.

Chromosomal Instability Index
For a given subject, we computed the median of the absolute value of the smoothed, segmented copy number values in each chromosome arm. The median of the arm-specific medians was defined to be the chromosomal instability index, which is similar to the definition that appears in [11].

Cancer Cell Line Data
CN and GE data are available for 18 esophagus and 19 upper aerodigestive tract cell lines that were classified as squamous cell carcinoma in the Cancer Cell Line Encyclopedia [30]. GE data in the cell lines are available for 803 of the 840 genes in our classifier. After restricting to these common genes, we normalized the GE data for the cell lines so that it had the same gene-specific means and standard deviations as in our classifier. We then used the centroid-based method described above to predict expression subtypes for the cell lines.

Data Availability
GE, CN, and select clinical data are available from GEO (accession number GSE39368). Copy number plots show that genomic events detected in the UNC HNSCC cohort can also be found in the HNSCC cell lines from the Cancer Cell Line Encyclopedia. A. Amplifications in chromosome 3q are seen in all predicted subtypes, and the predicted classical subtype exhibits focal amplification of the region containing SOX2. B. SCC15 (predicted basal) exhibits focal amplification of EGFR, while HS840T (predicted atypical) has normal copy number. C. Both KYSE140 (predicted mesenchymal) and KYSE70 (predicted classical) exhibit focal deletion of CDKN2A. D. Both FADU (predicted mesenchymal) and SCC15 (predicted basal) exhibit focal amplification of CCND1. Note that gains of 11q22 are also seen for SCC15. (TIF)

Supporting Information
Table S1 Differentially Expressed Genes in the Expression Subtypes. The R package samr was used to identify genes that were differentially expressed when each subtype was compared to all other subtypes combined based on an FDR threshold of q = .01. (XLSX) Table S2 Biological Characteristics of Expression Subtypes. Table S1 lists genes that were differentially expressed when each subtype was compared to all other subtypes combined. Biological characteristics and molecular pathways representative of the highly expressed genes were then identified, as were other relevant genes (e.g. growth/transcription factors). (DOCX)  Unadjusted Kruskal-Wallis Test p-values are given for associations between expression subtype and subject-specific mean copy numbers in the confidence intervals containing the five most significant gain and loss events. Adjusted p-values were computed using a Bonferroni adjustment (ten tests). (DOCX)