Abstract
Chromosomal instability (CIN) results in the accumulation of large-scale losses, gains and rearrangements of DNA1. The broad genomic complexity caused by CIN is a hallmark of cancer2; however, there is no systematic framework to measure different types of CIN and their effect on clinical phenotypes pan-cancer. Here we evaluate the extent, diversity and origin of CIN across 7,880 tumours representing 33 cancer types. We present a compendium of 17 copy number signatures that characterize specific types of CIN, with putative aetiologies supported by multiple independent data sources. The signatures predict drug response and identify new drug targets. Our framework refines the understanding of impaired homologous recombination, which is one of the most therapeutically targetable types of CIN. Our results illuminate a fundamental structure underlying genomic complexity in human cancers and provide a resource to guide future CIN research.
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Data availability
All data used in this study were obtained from publicly available sources and are described in detail in Supplementary Table 1, section ‘Data and Code’ in the Supplementary Methods. Some raw data have restricted access (TCGA dbGaP accession number: phs000178.v11.p8; ICGC EGA accession number: EGAS00001001692). Access can be obtained by applying to the relevant Data Access Committees (TCGA or ICGC). The authors declare that all other data supporting the findings of this study, including the source data for all figures, are publicly available without restrictions and are also available in the Supplementary Information and the Github repositories. All data supporting the analysis of our copy number signatures are navigable via our web portal (https://markowetz.cruk.cam.ac.uk/cincompendium/).
Code availability
The code is publicly accessible via our hub repository (https://github.com/markowetzlab/Drews2022_CIN_Compendium), which describes how the CIN signatures were derived and how to reproduce the figures and tables in this publication. The repository also contains the publicly accessible data and intermediary results used and produced in this study. The hub repository links to other repositories containing the code for specialized tasks.
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Acknowledgements
We thank M. Eldridge for setting up the online resource and A. Berman for bug fixes. R.M.D., P.S.S., D.-L.C., J.D.B. and F.M. are funded by Cancer Research UK (core grants C14303/A17197, A22905 and A19274) and the Cambridge Cancer Centre (grant C9685/A25117). G.M. and B.H. are hosted by the Centro Nacional de Investigaciones Oncológicas (CNIO), which is supported by the Instituto de Salud Carlos III and recognized as a ‘Severo Ochoa’ Centre of Excellence (ref. CEX2019-000891-S) by the Spanish Ministry of Science and Innovation (MCIN/AEI/ 10.13039/501100011033). G.M. and B.H. were also supported by a Spanish Ministry of Science and Innovation grant PID2019-111356RA-I00 (MCIN/AEI/ 10.13039/501100011033). M.T. was supported as a postdoctoral researcher of the F.R.S.-FNRS. L.M.G. was supported by the Wellcome Trust PhD programme in Mathematical Genomics and Medicine (grant number RG92770). M.S. was supported by the Horizon 2020 (H2020) Integrated Training Network CONTRA (grant 766030-CONTRA-H2020-MSCA-ITN-2017). This work was supported by the Francis Crick Institute, which receives its core funding from Cancer Research UK (FC001202), the UK Medical Research Council (FC001202) and the Wellcome Trust (FC001202). P.V.L. is a Winton Group Leader in recognition of the Winton Charitable Foundation’s support towards the establishment of The Francis Crick Institute.
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Contributions
G.M. and F.M. contributed equally to this work. R.M.D., G.M. and F.M. conceived and designed the study. R.M.D., B.H., D.-L.C., M.S. and G.M. developed the methodology of the study. R.M.D., B.H., M.T., K.H., T.L., P.S.S., L.M.G., L.L., M.S. and G.M. developed the software for the study. R.M.D., M.T., K.H., T.L., P.S.S., D.-L.C. and G.M. contributed to the validation of the method and results. R.M.D., B.H., L.M.G., D.-L.C., L.L. and G.M. contributed to the formal analysis presented in this study. R.M.D., B.H., K.H., T.L., P.S.S., L.M.G. and P.V.L. provided access to data and contributed to gathering, processing and curating data. R.M.D., J.D.B., P.V.L., G.M. and F.M. wrote the original draft. R.M.D., B.H., G.M. and F.M. produced and contributed to the visualizations of the study. R.M.D., G.M. and F.M. supervised the project. All authors had access to all of the data in the study. All authors contributed to the review and the editing of the manuscript. All authors approved the manuscript before the initial submission and all other resubmissions.
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J.D.B., G.M., F.M. are co-founders, directors and share holders of Tailor Bio Ltd. Cancer Research UK, the University of Cambridge and the Spanish National Cancer Research Centre (CNIO) are in the process of applying for a patent application GB2114203.9 covering the copy number signature methodology and drug target associations that lists R.M.D., B.H., G.M. and F.M. as inventors. G.M., F.M. and J.D.B are listed on a patent on using copy number signatures to predict response to doxorubicin treatment in ovarian cancer (PCT/EP2021/065058).
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Extended data figures and tables
Extended Data Fig. 1 Workflow of sample filtering and detectable chromosomal instability (dCIN).
a, REMARK diagram showing flow of samples through the study. b, For each copy number feature of the previous ovarian signatures: a histogram of number of events per sample that could not be assigned to an ovarian copy number signature on the TCGA ovarian cohort. Red dotted line indicates the quantile 0.95. c, Scatterplot of cancer types comparing our estimate of detectable CIN (Supplementary Methods) to estimates reported in the Mitelman database. d,e, Boxplots comparing our estimate of detectable CIN with aneuploidy score and four CNA-specific metrics. Boxes represent the interquartile range (IQR) with the median as a bolded line. The whiskers extend to the largest/smallest value no further than 1.5 * IQR from the hinge. Outliers beyond the end of the whiskers are marked individually as points. Results of two-sided Welch’s t-test shown on top of the boxplots.
Extended Data Fig. 2 Overview of copy number features and signature identification.
a, A schematic showing the 5 fundamental copy number features that were computed using 6,335 samples with detectable CIN (dCIN). Note, a feature capturing absolute copy number is not included in our method. b, A schematic showing how mixture modelling is used to split the genome-wide feature distributions into smaller components by either Variational Bayes Gaussian mixture models or Finite Poisson mixture models. The actual number of resulting components is listed below each feature distribution. These components represent basic building blocks of each feature distribution. c, An example of how the probability of a CNA belonging to a mixture component (posterior probability) is calculated and how these are summed. d, (Right) The resulting 43-dimensional feature vectors for each sample, after all posterior probabilities are summed for each component. (Left) A schematic of how the sum-of-posterior matrix for all 6,335 samples was split in two matrices by a Bayesian implementation of the non-negative matrix factorisation (NMF), resulting in a signature catalogue and an activity catalogue.
Extended Data Fig. 3 Schematic of the signature compendium identification.
a, From the complete input matrix 10 pan-cancer signatures were identified. b, For the 20 cancer types with over 100 samples each, 128 cancer-type enriched signatures (CTES) were identified. c, All CTES were removed that had a cosine similarity over 0.74 with any pan-cancer signature. d, From the groups of CTES that had cosine similarities over 0.74 to each other, the signature with activities in the largest number of samples was taken as a representative signature. e, We performed non-negative least squares on each pair of pan-cancer specific signatures to each CTES. For any combination which showed a reconstruction error below 0.1, this CTES was removed. f, The sets of 10 pan-cancer and 7 CTES were joined to a compendium of 17 signatures. g, Using linear combination decomposition, the signature activities were calculated for the 6,335 TCGA samples.
Extended Data Fig. 4 Signature interpretation matrix.
Displayed on the left are the five features, their mixture components and component means. The heatmap on the right shows the signature interpretation values, which combine information from the sum-of-posterior matrix, signature activity matrix and the signature definition matrix (Supplementary Methods). Only components that are positively correlated with signature activity levels are displayed. Interpretation values are normalised per feature and signature.
Extended Data Fig. 5 Monte Carlo simulation results for determining signature-specific noise thresholds.
a, Each plot (1 per signature) shows the interquartile range of sample signature activities after the introduction of noise in the copy number features using a Monte Carlo simulation. Samples are ordered by their observed signature activity (red line). b, Schematic showing how we fitted a Gaussian distribution to the simulated values of all samples with an observed signature activity of 0 (red line). The horizontal black line represents the quantile 0.95 of the fitted Gaussian and forms the basis of our signature specific noise threshold, where values below this line are not distinguishable from 0. c, Plot of the signature-specific thresholds for the 17 copy number signatures.
Extended Data Fig. 6 Signature stability across different copy number profiling technologies.
Across the same set of 478 tumours, we compared the SNP6-array based copy number profiles and signatures to copy number profiles and signatures derived using different copy number profiling technologies. The columns contain results for the different technologies and the rows contain results for comparison between copy number profiles (top), signature activities (middle) and signature definitions (bottom, limited to pan-cancer signatures). For each comparison we show results for a range of penalties for ASCAT’s piecewise constant fitting or ASCAT.sc’s circular binary segmentation. (*): For settings marked with a star it was not possible to derive solutions for K = 10, instead the optimal number of K was chosen (lower than K = 10).
Extended Data Fig. 7 Workflow for determining signature aetiology and confidence rating.
a, Flowchart showing how an association between a mutated gene and signature activity was used to derive a hypothesis for a putative aetiology. b, Flowchart representing the decision making process leading to the assignment of a 3-star rating confidence score. c, Example of the star rating process for CX3.
Extended Data Fig. 8 Summary of associations between signatures and other covariates.
a, Main panel shows significant associations between copy number signatures and mutated genes. Gene annotations summarised in the panels below. Boxes with a red line indicate significant associations that were not considered when determining signature aetiologies as the significant enrichment was via amplification of the gene, which also resided in an ecDNA amplicon, which could be a consequence of the signature rather than a cause, potentially causing a spurious correlation with amplification signatures (CX8, CX9, CX11, CX13). b, Each row shows highly significant associations between signatures and different covariates. Unless otherwise specified, only positive correlations are shown.
Extended Data Fig. 9 Impaired homologous recombination signatures and their associations.
a, Boxplots summarise signature activities of different patient groups (rows) defined by their driver gene mutation status. Ovarian samples are coloured in dark green and breast in orange. Boxes represent the interquartile range (IQR) with the median as a bolded line. The whiskers extend to the largest/smallest value no further than 1.5 * IQR from the hinge. Outliers beyond the end of the whiskers are marked individually as points. Significance tested with two-sided Welch’s t-test between WT BRCA1/2 and each of the categories and corrected for multiple testing by using Benjamini-Hochberg method. Statistically significant comparisons are shown to the right of the boxplots with stars denoting significance (q < 0.05) and arrows denoting the two groups used for the statistical test. (BRCA1/2 = BRCA1 and BRCA2, WT = wild type; LOH = loss of heterozygosity). b, Boxplots (with same characteristics as in a) summarise the scaled signature activities of 5,466 TCGA samples split by low, medium and high cell cycle scores. The brackets and stars (q < 0.05) show where there was a significant increase from low to medium to high cell cycle groups tested with a Welch’s t-test and corrected for multiple testing with Benjamini-Hochberg method. c, Volcano plots showing the results of a correlation between signature activity and expression of genes involved in nucleotide excision repair (NER). Each dot represents a gene, coloured dots show significant correlations. d, Spearman correlation coefficient (y-axis) of correlation between signature activities and seven common metrics of HRD (listed at top). Individual coefficients are displayed for impaired homologous recombination (IHR) signatures and the distribution of coefficients from remaining signatures are represented by boxplots (with same characteristics as in a).
Extended Data Fig. 10 Performance of classifiers for predicting platinum sensitivity.
a, Kaplan-Meier estimator showing the overall survival probabilities of TCGA ovarian cancer patients split into two groups using our CX3/CX2 classifier. b, Hazard ratios and their 95% confidence interval obtained from a Cox proportional hazards model trained on our CX3/CX2 classification predicting overall survival of TCGA ovarian cancer patients. The model also corrected for age and cancer stage of the patients. P-value represents the significance of a Wald test. c,d, Median survival and hazard ratios generated for five cancer cohorts from the TCGA, PCAWG and ICGC projects using predictions from three classifiers (our CX3/CX2 classifier, HRDetect and Myriad myChoice based on the HRD score). Improvements in median survival tested by log-rank test (Kaplan-Meier survival analysis), with the minus symbol representing the predicted resistant group and the plus symbol the predicted sensitive group. Hazard ratios, their 95% confidence interval, and Wald test significance of the predicted sensitive group compared to the predicted resistant group are obtained from Cox proportional hazards models correcting for stage and age of patients, except for HRDetect where tumour stage was omitted as the models did not converge if included. The number and proportion of patients predicted to be sensitive (with HRD) and resistant (without HRD) by each classifier are listed on the right.
Supplementary information
Supplementary Methods
This file contains full descriptions of all methods, links to software, additional results and Supplementary Tables 1–13.
Supplementary Figures
This file contains Supplementary Figs. 1–54.
Supplementary Tables
This zip folder contains Supplementary Tables 14-64 and their accompanying legends.
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Drews, R.M., Hernando, B., Tarabichi, M. et al. A pan-cancer compendium of chromosomal instability. Nature 606, 976–983 (2022). https://doi.org/10.1038/s41586-022-04789-9
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DOI: https://doi.org/10.1038/s41586-022-04789-9
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