Triple-negative breast cancers (TNBC) lack estrogen and progesterone receptors and HER2 amplification, and are resistant to therapies that target these receptors. Tumors from TNBC patients are heterogeneous based on genetic variations, tumor histology, and clinical outcomes. We used high throughput genomic data for TNBC patients (n = 137) from TCGA to characterize inter-tumor heterogeneity. Similarity network fusion (SNF)-based integrative clustering combining gene expression, miRNA expression, and copy number variation, revealed three distinct patient clusters. Integrating multiple types of data resulted in more distinct clusters than analyses with a single datatype. Whereas most TNBCs are classified by PAM50 as basal subtype, one of the clusters was enriched in the non-basal PAM50 subtypes, exhibited more aggressive clinical features and had a distinctive signature of oncogenic mutations, miRNAs and expressed genes. Our analyses provide a new classification scheme for TNBC based on multiple omics datasets and provide insight into molecular features that underlie TNBC heterogeneity.
Breast cancer is heterogeneous in nature, as breast tumors can arise from different cells of origin, and can present with distinct mutational signatures, biological and clinical phenotypes, and survival outcomes1,2,3. Breast tumors have been categorized clinically based on histological analyses of the levels of two hormonal receptors, estrogen (ER) and progesterone (PR), and human epidermal growth factor receptor 2 (HER2) amplification4. This classification system has been proven to have predictive power about a patient’s prognosis and is routinely used to make decisions about therapy. Perou et al. analyzed the inter-tumor heterogeneity in breast cancer using microarrays and developed a classification system that defined intrinsic subtypes (luminal A, luminal B, HER2-enriched, basal-like, and normal)5. New breast tumors can now be assigned to one of these classes based on the expression pattern of 50 informative genes termed PAM50 (ref.5). These breast cancer subtypes have different molecular characteristics and clinical outcomes6. Luminal A has the best clinical outcome. Comparing luminal A and luminal B tumors, luminal B tumors have higher expression of cell cycle and cell proliferation genes, lower expression of luminal genes such as PR, higher mutational burden and more copy number changes. HER2-enriched tumors have the highest mutational burden of all subtypes and display high expression levels of HER2-regulated and cell proliferation genes. Basal-like tumors highly express cytokeratins that are usually present in the basal cells of normal breast, and cell proliferation genes. Another intrinsic subtype called claudin-low was subsequently identified7. The claudin-low subtype is associated with signatures related to mammary stem cells and epithelial-to-mesenchymal transition. In a large-scale study (~500 breast cancer patients) by The Cancer Genome Atlas (TCGA), the authors sought to identify breast cancer subtypes based on a combination of genomic, mutational, and epigenetic signatures. This study revealed four groups that showed high concordance with the four intrinsic PAM50 subtypes8.
The majority of breast cancers (80–85%) are positive for hormonal receptors and/or HER2 amplification, and therefore respond to therapies that target these markers6. Triple negative breast cancer (TNBC) is clinically defined based on the absence of the estrogen and progesterone receptor, and HER2 overexpression. TNBC constitutes approximately 16% of breast cancer cases9. It is a particularly proliferative and aggressive subtype of breast cancer, associated with large size, high tumor grade, high mitotic rate, and metastasis10. Because of the lack of druggable targets, TNBC are treated with conventional chemotherapy, and only approximately 50% of patients respond11. The 5-year survival rate is only 14%12, much worse than for other breast cancer subtypes. TNBC are more prevalent in young women and in women of African or Hispanic descent13.
TNBC demonstrates genomic heterogeneity, as there is a substantial variation in mutational burden, copy number alterations, and genomic rearrangements across TNBC patients14,15,16. In contrast to other types of breast cancer in which several genes are mutated at high frequency, only two genes (TP53 and PIK3CA) are mutated in >10% of TNBC patients16,17. Thus, there are many different oncogenic drivers of TNBC. TNBC also demonstrates histological heterogeneity as nine different histologic subtypes have been identified based on immunohistochemistry (IHC), with invasive ductal carcinoma being the most prevalent type15,16.
Understanding the molecular basis of TNBC heterogeneity will be important for the development of precision therapy that targets specific molecular markers present in some TNBCs (genes, miRNAs etc.). Previous studies have defined subtypes of TNBC based on gene expression18,19,20,21. Most TNBCs are classified as basal-like subtype based on PAM50 gene expression signatures19. Further classification schemes focused more specifically on TNBC have also been developed. Lehmann et al.18 and Burstein et al.20 identified six and four TNBC subtypes, respectively, using microarray analysis. The six subtypes defined by Lehmann et al. have unique gene expression signatures and respond differently to chemotherapy. Some of the gene expression signatures associated with two (immunomodulatory and mesenchymal stem-like) of the six subtypes likely reflect the presence of cells from the tumor microenvironment, rather than the cancer cells themselves19,21. To address this, Lehmann et al. recently published a revised classification containing four TNBC subtypes (basal-like 1 (BL1), basal-like 2 (BL2), mesenchymal (M), and luminal androgen receptor (LAR)) using RNA-seq data from TCGA21. The survival outcome of patients with the BL1 subtype was found to be significantly better than the survival for patients from the other three subtypes combined.
Inter-tumor heterogeneity for breast cancers, including TNBC, has been measured mainly by clustering tumors based on gene expression data from microarray or RNA sequencing methods. The availability of data from other sources (miRNA, DNA methylation, CNVs, protein arrays) has provided new avenues to understand tumor heterogeneity. Recently, three TNBC subtypes based on DNA methylation sequencing have been proposed and shown to have different clinical courses22. Integrative clustering methods23,24 combining gene expression data with other data types such miRNAs and CNVs have been performed to identify novel subtypes for breast25,26 and other tumors27. Integrative approaches have been shown to be more robust in comparison to methods using biomarkers of one type only23. To date, methods that integrate different datatypes have not been applied to understand TNBC heterogeneity.
Given the clinical importance of TNBC and the clear need for classification systems that capture the inter-tumor heterogeneity of TNBC in a comprehensive manner, we performed integrative clustering combining information from multiple types of omics data (gene expression, miRNA expression, and CNV) collected from TNBC tumors. This led to the identification of three TNBC clusters with distinct molecular and clinical features. This new classification scheme may have implications for the treatment of TNBC.
Selection of TNBC patients
Out of 1098 breast invasive carcinomas in the TCGA database, 180 have been classified as triple-negative by Lehmann et al. based on low expression levels of ER, PR, and HER221. In addition to the cancer cells, a tumor sample may contain cells from the tumor microenvironment (TME), such as fibroblasts, endothelial cells, and immune cells. The presence of these cells may confound the signals originating from cancer cells. Sequencing data provided by TCGA were collected from only those cancer tissues with >60% cancer cells (>60% tumor purity) as determined by counting the tumor nuclei28. Recently, more refined computational methods using sequencing data (gene expression, methylation, and CNV) have been used to estimate tumor purity by taking into account the contribution of non-cancer cells29. Aran et al. provided consensus purity estimations (CPE) based on a combination of four methods—gene expression of non-cancer cells, somatic CNVs, immune-related methylation pattern, and immunohistochemical analysis. In an independent analysis, tumor purity scores (from Clonal Heterogeneity Analysis Tool (CHAT)) for the same tumors were determined based on an analysis of copy number alterations30,31. For this study, we only included those TNBC primary tumors for which the tumor purity scores were estimated to be >60% by either Aran et al. or Li et al. (Supplementary Table S1). One hundred thirty-seven out of 180 TNBC tumors met these criteria. About 39% of these patients were 50 years of age or younger (Table 1) and most of these patients (76%) had tumors that were classified as basal-like PAM50 subtype.
Single-data clustering to determine TNBC heterogeneity
In order to assess inter-patient heterogeneity among the TNBC samples, we performed consensus clustering (combining clustering information from different runs into one cluster)32 of patients using non-negative matrix factorization (NMF)33. Consensus clustering was performed separately using gene expression (RNA-seq), miRNA expression (miRNA-seq), and copy number variants (CNV) (SNP 6.0 array) data provided by TCGA (Fig. 1, see Methods). Consensus clustering was performed on the subset of genes, miRNAs, and CNVs with the largest variation across the patients (pre-selection step, Fig. 1).
Gene expression-based NMF clustering was performed on 137 patients using two different distance metrics: Kullback-Leibler and Euclidean. To test the quality of the clusters, three different validation metrics34 were applied that analyzed the degree of cluster compactness (RMSSTD, r-squared) and cluster separation (SD validity index). Out of two distance metrics, the Euclidean metric performed the best based on top scores in all the three validation tests (Supplementary Table S2). For Euclidean metric-based clustering (NMF-gene), the optimal number of clusters was determined to be four (see Methods) (Supplementary Fig. S1). We also performed single-data clustering using miRNA expression and CNV data obtained from TCGA (Fig. 1). For both of these data types, the Euclidean distance metric again provided the best solution (Supplementary Table S2). Four and three cluster solutions were considered optimal for miRNA-based (NMF-miRNA) and CNV-based (NMF-CNV) clustering, respectively, using the Euclidean distance metric (Supplementary Fig. S1).
Comparison of the best NMF clustering solutions obtained from three data types (NMF-gene, NMF-miRNA, and NMF-CNV) did not show much agreement as indicated by very low (NMF-gene/NMF-miRNA and NMF-miRNA/NMF-CNV) and negative (NMF-gene/NMF-CNV) adjusted rand index scores35 (a metric of the similarity between two clustering solutions) (Fig. 2A). To gain further insight into these single-data NMF clusters, we determined the signature genes, miRNAs, and CNVs that displayed the largest variation between the clusters for NMF-gene (1187 genes), NMF-miRNA (61 miRNAs), and NMF-CNV (2044 CNVs), respectively (see Methods). This identified gene sets 1 and 2, miRNA set 1, and CNV set 1 that showed prominent variation between the clusters (Fig. 2B). Thus, different data-types captured different information about the heterogeneity in TNBC tumors.
Comparison of single-data clusters with PAM50 and Lehmann subtypes
For each of the NMF-miRNA and NMF-CNV clusters, more than half of the tumors were classified as basal-like PAM50 subtype (Supplementary Fig. S2). The fraction of basal-like tumors in these clusters ranged from 57–84% for miRNA-based clusters and 70–81% for CNV-based clusters. For NMF-gene clustering, the fraction of basal-like tumors in three out of four clusters was found to be >65% (Supplementary Fig. S2). These results agree with previous studies showing TNBC tumors to be predominantly of basal-like subtype19. The clustering indicates heterogeneity within the basal-like subtype as these tumors did not cluster together, but rather were split into separate clusters. One exception among single-data clusters was cluster 4 of the NMF-gene classification (Supplementary Fig. S2). The tumors in this cluster were composed primarily of luminal A (38%) and HER2-enriched (25%) subtypes. Among the NMF clusters, the NMF-gene clusters correlated best with Lehmann subtypes, which were developed based on gene expression data (Supplementary Fig. S2). The majority of patient tumors from cluster 1 were M subtype; the majority of patients in cluster 3 were basal-like; and the majority of the patients in cluster 4 were LAR.
Integrative clustering of TNBC patients
Integrative clustering methods that combine different data types are based on more “information content” than methods that rely on a single data clustering23. They consequently have the potential to provide a comprehensive view of inter-tumor heterogeneity. The low concordance among the single-data clusters from the three data types (Fig. 2A) suggests that the different data types capture the variation among the tumors in different ways. We reasoned that integrative clustering might be better suited for TNBC classification because it would combine information from the three data types. The similarity network fusion (SNF) method36 was used to integrate gene, miRNA, and CNV data from 134 TNBC patients. Each of the three data types was first used to construct individual patient networks. These networks were then combined to generate a single fused network. Spectral clustering was then performed on this fused network to reveal patient clusters or subtypes. In contrast to single-data clustering (Fig. 1), no pre-selection of genes, miRNAs, or CNVs was required for SNF analysis, thus removing any bias due to a pre-selection step.
SNF-based clustering produced three clusters (SNF clusters 1–3) upon combining gene, miRNA, and CNV data (Fig. 3A). The three SNF clusters were less distinct when considering patient networks based on a single data type (Fig. 3B,C and E). Coverage scores (ratio of intra-cluster edges to total edges)37 for SNF clusters showed higher coverage for the fused patient network constructed using the combination of three data types (gene + miRNA + CNV, 85%) compared to those generated by single-data types (gene only, 69%; miRNA only, 67%; and CNV only, 58%). The higher fraction of edges connecting the nodes within the clusters for the fused network indicates better separation (lower fraction of inter-cluster edges) compared to single-data types. The separations among SNF clusters 1–3 were maintained when DNA methylation data was incorporated with gene, miRNA, and CNV data (see Methods) to generate the fused network (Supplementary Fig. S3).
Comparison of SNF clusters with single-data clusters, PAM50, and Lehmann classifications
The clusters generated by an integration of the three datatypes did not correspond to the clusters generated with any single datatype using NMF clustering methods. SNF Cluster 2 had the most overlap with NMF-gene cluster 4 (71%), NMF-miRNA cluster 4 (68%), and NMF-CNV cluster 1 (71%) (Supplementary Fig. S4). Most of the patient tumors in SNF cluster 3 were assigned to NMF-gene cluster 1 (63%) and NMF-miRNA cluster 1 (63%). There was no major overlap (>50%) of SNF cluster 1 with any of the single-data clusters.
The SNF clusters that we generated did not align with the PAM50 intrinsic subtypes defined for all breast cancers (Fig. 4A) or the subtypes defined by Lehmann et al. specifically for TNBC (Fig. 4B). Of the three SNF clusters, the fraction of tumors with a basal-like subtype classification based on PAM50 was least for cluster 2 (41%) compared to clusters 1 (86%) and 3 (92%) (Fig. 4A). Cluster 2 had higher fractions of HER2 (18%) and luminal (32%) PAM50 subtypes compared to clusters 1 (0% HER2 and 4% luminal) and 3 (0% HER2 and 8% luminal). When compared with the Lehmann subtypes (Fig. 4B), clusters 1 and 3 were mainly composed of basal-like 1 (47%) and mesenchymal subtypes (65%), respectively, while basal-like 2 (38%) and luminal androgen receptor subtypes (50%) represented the majority of the tumors in cluster 2. The SNF clusters we generated did share a similarity to NMF-gene clusters (Supplementary Fig. S2) and Lehmann subtypes21 in that they all contained a cluster (cluster 4 of NMF-gene and LAR subtype by Lehmann et al.) that was enriched in HER2 and luminal PAM50 subtypes, with the rest of the clusters containing a high fraction of tumors with a basal-like subtype.
Clinical properties of SNF clusters
SNF cluster 2 had a greater fraction of patients (26%) with larger tumor size (tumor score of T3 and T4 in TNM staging system), compared to clusters 1 (11%) or 3 (4%) (p = 0.03, Fisher’s exact test) (Fig. 4C). Higher T numbers (T3 and T4) indicate larger tumor size and/or greater extent of tumor growth into nearby tissues38. Thirty two percent of cluster 2 patients had tumors of higher pathologic stage (stages III and IV). In comparison, only 9% and 15% of cluster 1 and cluster 3 patient tumors, respectively, were of stage III and stage IV (p = 0.01, Fisher’s exact test) (Fig. 4D). In addition to tumor size, pathologic stage is also dictated by regional lymph node and distant organ metastasis38. Disease-free survival analysis revealed that cluster 2 TNBC patients (n = 34) had poorer disease-free survival (p = 0.000024) compared to the remaining breast cancer patient cohort from TCGA (breast invasive carcinomas, n = 1098) (Fig. 4E). In contrast, no significant difference was found between disease-free survival for clusters 1 (n = 74) or 3 (n = 26) compared with the remaining breast cancer patient cohort.
Differentially expressed genes and miRNAs between SNF clusters
In order to understand the biological basis for the segregation of the TNBC tumors into the clusters generated with integrated SNF clustering, we ranked the features (genes, miRNAs, and CNVs) based on their normalized mutual information (NMI) scores36 (see Methods section of Cavalli et al.27). These scores (Supplementary Table S3) provide a measure of the importance of different features for the construction of the fused network obtained by SNF. Analysis of all the features with the top-ranked NMI scores (top 1% genes, top 5% miRNAs, and top 5% CNVs) across the three SNF clusters revealed a subset of genes and miRNAs (gene set 1, gene set 2, and miRNA set 1) that were differentially expressed in cluster 2 compared to clusters 1 and 3 (Fig. 5). Thus, the top-ranked NMI features contributed more toward separation of cluster 2 from clusters 1 and 3. The 605 genes with the top 1% NMI scores (Fig. 5A) were enriched for genes related to transcriptional regulation, mesenchymal cell differentiation, embryo development and morphogenesis. The gene targets for the top 5% NMI-ranked miRNAs (94 miRNAs) (Fig. 5B) were involved in positive regulation of cellular and metabolic processes, development, and cell proliferation. The genes affected by the top 5% NMI-ranked CNVs (1809 CNVs) (Fig. 5C) participate in amino acid metabolism and phosphatidylcholine 1-acylhydrolase activity. These CNVs are mainly present on chromosomes 1, 5, and 14 (Supplementary Fig. S5). Out of 1809 CNVs, about 722 CNVs were not closely associated with any genes.
Analysis of the genes with the top NMI scores revealed differences between cluster 2 and clusters 1 and 3 (Fig. 5, gene sets 1 and 2 and miRNA set 1). In order to find signature genes specific to clusters 1, 2, and 3, we performed differential gene expression analysis for three cluster pairs (1 vs. 2, 2 vs. 3, and 1 vs. 3) and then extracted the genes that are specifically upregulated (up_1, up_2, and up_3) or downregulated (down_1, down_2, and down_3) in each of the three clusters (Supplementary Table S4 and Fig. 6). Of the top 100 NMI-scored genes, 68 were specifically upregulated (46 genes) or downregulated (22 genes) in cluster 2. This supports the importance of cluster 2-specific genes in determining the pattern of the fused patient network. The gene ontology (Supplementary Table S4) and pathway analysis (Fig. 6) suggests that different cellular pathways are activated in clusters 1, 2, and 3. For instance, the androgen receptor (AR) was specifically upregulated in cluster 2 (up_2, Supplementary Table S4). AR-dependent signaling is activated in tumors classified by Lehmann as LAR subtype39 and 50% of cluster 2 tumors are classified as LAR subtype (Fig. 6B). Pathway terms enriched among the genes induced in cluster 2 include “Rho GTPases activate PKNs” and “activated PKN1 stimulates transcription of AR regulated genes KLK1 and KLK2”, thus identifying a signaling pathway associated with androgen receptor expression upregulated in cluster 2. The expression of cluster 2 -specific genes (up_2 and down_2) was similar across the PAM50 and Lehmann subtypes (Supplementary Fig. S6).
The miRNAs specifically upregulated and downregulated in each of the three SNF clusters (Supplementary Table S5) were obtained using the same strategy used to extract cluster-specific genes. Fifty-two of the top 100 NMI-ranked miRNAs (38 upregulated and 14 downregulated) were unique to cluster 2. The oncogenic miRNA miR-10b was specifically upregulated in cluster 2. Overexpression of miR-10b in non-metastatic breast cancer cells has been shown to induce cancer cell invasion and metastasis, and expression of miR-10b in primary breast tumors is associated with metastasis40,41. Two tumor suppressor miRNAs41,42, miR-17 and miR-206, were downregulated in cluster 2. miR-17-5p targets amplified in breast cancer (AIB1), which in turn promotes cell proliferation43. miR-206 is downregulated in many cancers and has been shown to target K-Ras, annexin a2, and cell cycle genes44,45. Oncogenic miRNA miR-9 (produced from the mir-9-3 locus) was upregulated in cluster 346. miR-9 targets E-cadherin and thereby promotes cell migration and invasion. As with genes, the expression of cluster 2-specific miRNAs (up_2 and down_2) did not vary depending on PAM50 and Lehmann subtypes (Supplementary Fig. S6).
Structural variations and mutational profile of SNF clusters
Genomic alterations such as single-base mutations and CNVs (covering regions >1 kilobase) are important drivers of carcinogenesis and can maintain the fitness of cancer cells47,48. These alterations are a potential source of inter-tumor heterogeneity. We determined the extent of gene amplifications due to CNVs in the tumors that constitute the three SNF clusters (Supplementary Table S6). Clusters 1 and 3 had 126 genes and 168 genes with amplification frequencies above 10%, respectively. In contrast, only 28 genes were altered with >10% frequency in cluster 2.
In addition to CNVs, activating and inactivating mutations can also serve as oncogenic drivers. Mutational analysis showed that tumor protein p53 (TP53) and titin (TTN) were commonly mutated in tumors in all three clusters with frequencies ranging from 63–78% and 23–27%, respectively (Supplementary Table S6). Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) was mutated at higher frequency in cluster 2 (23%) compared to clusters 1 (3%) and 3 (8%). Cluster 2 tumors contain a higher frequency of AR-positive tumors, and PIK3CA is frequently mutated in AR-positive tumors39,49.
Predictive modeling and biological properties of predictors
Because the three SNF clusters have different biological and clinical properties, the ability to assign a new tumor to one of the three existing clusters could be beneficial for patients with TNBC. We sought to develop a classifier (see Methods) that would assign a new TNBC patient to one of the SNF clusters based on the patient’s mRNA, miRNA, and CNV data. The workflow for training and testing the classifier is shown in Fig. 7A. We divided the 134 patients used for SNF clustering into a training set (n = 95) for developing the classifier and a test set (n = 39) for classifier testing. We trained three different classifiers (random forest, elastic net logistic regression, and support vector machine) and evaluated their performances. The elastic net logistic regression had the highest accuracy (90%) and F1 score metrics (see Methods) (Fig. 7B and Supplementary Table S7). The accuracy for random forest and support vector classifiers were 79% and 87%, respectively. When applied to a test data set not used for training, the elastic net logistic regression classifer was able to correctly predict 35 out of 39 patient labels (clusters 1–3) indicating an accuracy of 90% (Fig. 7C). This classifier (see Methods) could be used to identify the cluster label of TNBC patients if gene, miRNA, and CNV data were available.
The breast epithelial layer consists of an inner layer of luminal cells and an outer layer of basal or myoepithelial cells50. Gene expression-based PAM50 intrinsic classification of breast cancer5 includes basal-like and luminal A/B subtypes, and two models have been proposed to explain the cellular origin of these tumor subtypes50. In the cell of origin model, luminal tumors originate from committed late progenitors of luminal cells, while basal tumors originate from early progenitors of luminal cells. The alternative genetic mutation model postulates that luminal and basal-like tumors result from different genetic insults acting upon similar populations of luminal progenitors. With this model, TNBC tumors result from additional changes that lead to a loss of expression of ER and PR in tumors without amplification of HER2. Much less is known about the origin of HER2-enriched PAM50 subtype. The tumors in this subtype are heterogeneous with respect to the expression of hormonal receptors (ER and PR) and only 70% of these tumors are classified as HER2+, suggesting a different cell of origin of these tumors50.
Using an integrative approach to clustering, we discovered that we could classify TNBC tumors into three distinct tumor clusters using a combination of gene, miRNA, and CNV data. Comparison of our integrative clusters with the PAM50 subtypes revealed that integrative clusters contained a mixture of tumors from multiple PAM50 subtypes. Cluster 1 and cluster 3 had a similar composition of tumors based on PAM50 classification. Tumors from both clusters were 80–90% basal-like, which is the subtype often associated with triple negative breast cancer, and contained a small amount of luminal A (4–8%), with normal making up the rest (Fig. 4A). In contrast, cluster 2 had the worst clinical features and disease outcome out of all the three integrative clusters, and the lowest proportion of patients identified as PAM50 basal subtype (41%). This cluster contained the highest proportion of HER2-enriched (18%) and luminal A (26%), with smaller contributions from luminal B and normal (Fig. 4A). Thus, by interrogating different types of features (genes, miRNAs, and CNVs) and interactions among them, our clustering resulted in distinct clusters from those produced by the PAM50 gene expression-only approach. We interpret the relationship between our integrative clusters and PAM50 gene expression as supporting a model in which there are two quite distinct pathways to TNBC, one involving mostly basal cells and leading largely to tumors in integrative clusters 1 and 3, and another that can result from luminal or HER2-enriched cells, that we believe leads to tumors in integrative cluster 2. These two pathways may reflect a different cell of origin or differences in the most critical oncogenic drivers.
We also compared the three clusters generated by our integrative analysis with the four TNBC subtypes of the gene expression-based Lehmann classification21. Each of the integrative clusters contains tumors that had been assigned to multiple different Lehmann subtypes (Fig. 4B). Integrative cluster 1 includes more basal-like 1 (47%) than the other subtypes, with mesenchymal (28%) the second most frequent. Integrative cluster 2, the cluster with poor clinical properties, is enriched in luminal androgen receptor (50%) and basal-like 2 (38%) Lehmann subtypes. The basal-like 1 Lehmann subtype, which has the best survival outcome compared to the rest of the subtypes combined21, is least represented in integrative cluster 2 (3%), suggesting agreement of integrative clusters with Lehmann subtypes in terms of clinical characteristics of the TNBCs. Cluster 3 of the integrative clustering was most strongly enriched (>60%) in the mesenchymal Lehmann subtype, with basal-like 1 (27%) the next most abundant. Comparing all of the classifications, we observe that three out of four Lehmann subtypes (BL1, BL2, and M) mostly consisted of TNBCs that were assigned as basal-like PAM50 subtype, while the majority of LAR tumors were HER2-enriched and luminal PAM50 types. Therefore, clusters 1 and 3 were similar in being mostly comprised of tumors classified as basal-like by PAM50 and as either basal-like 1 or mesenchymal by Lehmann. Cluster 2 was enriched for basal-like 2 and luminal androgen receptor by Lehmann classification, making it distinct from clusters 1 and 3, a finding also supported by its low levels of basal-like tumors by PAM50. By generating cluster 2, our integrative clustering found similarities between tumors called basal, HER2-enriched or luminal A by PAM50, or basal-like 2, luminal androgen receptor or mesenchymal by Lehmann classification, that were not detected by previous clustering approaches. Our findings also suggest that there are global distinctions identified by the features we considered that lead to two distinct and separable groups (cluster 1 and cluster 3) among tumors that are assigned basal-like by PAM50 and basal-like 1 or mesenchymal by Lehmann.
Each integrative cluster had a distinct profile with regard to genes, microRNAs and CNVs. Cluster 2 was the most distinct and its gene expression signature included genes in the RhoA-PKN1-androgen receptor pathway. PIKC3 was more frequently mutated in the tumors in this cluster, while copy number variants and gene amplification events were relatively rare. Tumors in this cluster also contained higher levels of the oncogenic microRNA miR-10b. Clusters 1 and 3 were similar to each other in terms of being mostly basal PAM50-subtype, similar disease-free progression and tumor size, similar numbers of copy number variants, and a similar set of oncogenic mutations with frequent mutations in p53 and titin. Tumors in clusters 1 and 3 were most strongly differentiated by downregulation of genes associated with the nervous system and synaptic transmission in the tumors in cluster 1 and downregulation of genes associated with the complement pathway and the humoral immune response in cluster 3. The variable expression of neuronal genes in TNBC clusters 1–3 is surprising, but neuronal-specific markers have been reported to be expressed in breast cancer cell lines and primary tumor tissues, possibly due to an abnormal trans-differentiation process51.
TNBC patients do not respond to hormone-based or anti-HER2 therapies52 and treatment options are mostly limited to chemotherapy (neoadjuvant and adjuvant) and surgery. Furthermore, the heterogeneous nature of TNBC limits the efficacy of standard chemotherapeutic agents because the response to these treatments varies greatly among patients. A few targeted therapies for TNBC have been proposed, including mTOR inhibitors, FGFR inhibitors, and EGFR-directed antibodies such as cetuximab52. Our results include the discovery that the androgen receptor is expressed in tumors in cluster 2. This finding suggests there may be an opportunity to treat this group of patients with anti-androgens53. Also, we identified two oncogenic miRNAs, miR-10b and miR-9, that are specifically upregulated in clusters 2 and 3, respectively. Silencing of miR-10b using an antagomir oligonucleotide54 and silencing of miR-9 using a miRNA sponge46 have been shown to inhibit metastasis in mouse models of breast cancer.
Collectively, our results indicate that a new classification system for TNBC that addresses its inherent heterogeneity can be defined by an integrative clustering methodology that incorporates multiple different data types. With this approach, we identified specific molecular signatures for different TNBC clusters. The distinctiveness of the integrative clusters we identified in terms of their genetic and epigenetic properties, oncogenic drivers and clinical features suggests that this new cluster assignment could provide another perspective on TNBC heterogeneity.
Acquisition of patient data
All the sequencing and clinical data associated with TNBC patients (n = 180) were obtained from The Cancer Genome Atlas (TCGA) hosted by the Genomic Data Commons (GDC). Patients (n = 180) were identified as triple negative breast cancer patients based on the analysis performed by Lehmann et al.21. RNA-Seq and miRNA-Seq data were downloaded as raw counts. The CNV data from Affymetrix SNP 6.0 array was processed by GDC into output files containing segment mean values (transformed copy number values for each of the segmented genomic regions), which were used for this work. DNA methylation levels (as beta values) from Illumina Infinium Human Methylation 450 arrays (if available) were also obtained. (More information on GDC output files and pipelines can be found on the GDC website: https://docs.gdc.cancer.gov/.) Clinical metadata (Supplementary Table S1) were extracted from clinical XML files provided by GDC.
Purity estimates for the 180 TNBC tumors were obtained from Aran et al.55 and Li et al.30. Patients were kept in the study if they had a consensus purity estimate (CPE) (from Aran et al.) or Clonal Heterogeneity Analysis Tool (CHAT) (from Li et al.) purity measurement of 60% or higher. The purity scores are presented in Supplementary Table S1.
Single data type patient clustering
The workflow for single data type clustering is presented in Fig. 1. The raw reads (genes and miRNAs) were normalized and log2 transformed by DESeq256. The segment mean values for CNV events were processed and converted to a CNV region-by-patient matrix using the CNTools bioconductor package57. Standard deviation (sd) filters (sd >2, sd >1, and sd >0.5 for gene, miRNA, and CNV, respectively) were used to select the genes, miRNAs, and CNVs that showed maximum variation across the patients and, therefore, were indicative of TNBC inter-tumor heterogeneity. Applying these criteria led to the selection of 2587 genes, 369 miRNAs and 5000 CNVs. We applied consensus clustering using non-negative matrix factorization (NMF) as the underlying algorithm. NMF clustering was performed using the NMF bioconductor package58 with Euclidean and Kullback-Leibler divergence as distance measures. The cluster number was selected based on the values of cophentic correlation coefficient59, which is a metric for the stability of clusters58. We evaluated the cluster solutions from NMF methods by following internal validation metrics34: RMSSTD, r-squared and SD validity index.
Integrative clustering using gene, miRNA, and CNV data was performed using the similarity network fusion (SNF) method36 for the 134 patients for which all the data were available from TCGA. No preselection of genes, miRNAs, or CNVs was required for SNF method. The three data types were aggregated by SNFtool R package to generate a fused patient network and a fused patient similarity matrix using the following parameters: K = 13, alpha = 0.5, and t = 2036. Spectral clustering was performed on the fused patient similarity matrix using the function built into the SNF package. Cluster number was chosen using the supplied function, estimateNumberOfClustersGivenGraph. The networks were visualized in Cytoscape60 by generating a k-nearest neighbors graph from the values of the patient similarity matrix. Normalized mutual information (NMI) scores of the features (genes, miRNAs, and CNVs) were obtained as the output from SNFtools package using its rankFeaturesByNMI function. For the fused patient network generated using gene, miRNA, CNV, and DNA methylation data, only the 87 of 134 patients with associated methylation data were used.
Pathway Analysis of genes, miRNAs, and CNVs
Gene ontology (biological process and molecular function) and pathway analysis (based on KEGG61 and Reactome62 databases of cellular pathways) of genes was performed using g:Cocoa module of g:Profiler63. The statistical significance of the results after multiple testing correction was computed using the built-in g:SCS method. Only the results (enriched pathways) with p values <0.05 were considered significant. The gene targets for miRNAs were obtained from miRTarBase v6.064 and miRTex65. The genes present in the CNV regions were extracted using genomicRanges bioconductor package66. SNF cluster-specific data for genomic alterations (mutations and genes amplified or deleted by CNVs) were obtained from cBioPortal for Cancer Genomics67,68: http://www.cbioportal.org.
Differential expression analysis of genes and miRNAs
Differential gene and miRNA expression between the SNF cluster pairs (1 and 2, 2 and 3, and 1 and 3) was performed using DESeq2 bioconductor package56. Only the significant (adjusted p < 0.05) genes and miRNAs with absolute log2fold change >1 were selected. In order to find cluster-specific genes, we compared the log2fold-change values of the genes across the three pairwise differential expression analyses. Genes were considered specifically upregulated (downregulated) in one cluster if they were upregulated (downregulated) in that cluster compared to each of the other two clusters.
Classifiers were created using the caret package in R69. Initial predictors were selected by taking the top-ranked NMI features from the SNF network analysis (top 1% for genes and CNVs and top 5% for miRNA). A 70/30 split was applied to the data (n = 134) to create a training set (n = 94) and a test set (n = 40). Samples were selected for the training set by the partition function built into the caret software package. Predictor selection was performed on the training set by applying a Kruskal-Wallis test across the top NMI features (FDR < 0.01). Predictors that passed the significance test (525 genes, 112 miRNAs, and 1809 CNVs) were used for the classifiers. Three classifiers (supplied by the carat package) were trained: elastic net logistic regression (glmnet function), random forest (randomForest), and a linear kernel support vector machine (lmSVM). Leave-one-out cross validation (LOOCV) was used to further validate and tune model parameters and the resulting classifiers were evaluated using accuracy and average F1 scores (based on precision and recall) obtained from the carat package (Supplementary Table S7).
Statistical tests employed for each analysis are provided in the text and legends. For all analyses, we used adjusted p < 0.05 to determine statistical significance. p values are adjusted for multiple hypothesis testing. Tests are two-sided.
All the datasets used in the study are publicly available from NCI genomic data commons: https://gdc.cancer.gov/.
The software packages used in this study are listed in Supplementary Table S8. Further information is available upon request.
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The authors wish to thank Eleazar Eskin, the Hoffmann2 Cluster support group (Institute for Digital Research and Education) at UCLA, and the members of the Coller laboratory. HAC was the Milton E. Cassel scholar of the Rita Allen Foundation (http://www.ritaallenfoundation.org). This work was funded by grants to HAC from the PhRMA Foundation grant 2007RSGl9572, National Institute of General Medical Sciences R01 GM081686, National Institute of General Medical Sciences R01 GM0866465, the Eli & Edythe Broad Center of Regenerative Medicine & Stem Cell Research, the Iris Cantor Women’s Health Center/UCLA CTSI NIH Grant UL1TR000124, a Leukemia Lymphoma Society New Idea Award, Innovation Awards from the Broad Stem Cell Research Center (Rose Hills and Ha Gaba), an Award from the UCLA SPORE in Prostate Cancer (National Cancer Institute of the National Institutes of Health under Award Number P50CA092131), and an award from the Cancer Research Institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. HAC is a member of the Jonsson Comprehensive Cancer Center, the Eli & Edythe Broad Center of Regenerative Medicine & Stem Cell Research, the UCLA Molecular Biology Institute, and the UCLA Bioinformatics Interdepartmental Program.