Genomic alterations shape cell phenotypes and the structure of tumor ecosystems in poorly defined ways. To investigate these relationships, we used imaging mass cytometry to quantify the expression of 37 proteins with subcellular spatial resolution in 483 tumors from the METABRIC cohort. Single-cell analysis revealed cell phenotypes spanning epithelial, stromal and immune types. Distinct combinations of cell phenotypes and cell–cell interactions were associated with genomic subtypes of breast cancer. Epithelial luminal cell phenotypes separated into those predominantly impacted by mutations and those affected by copy number aberrations. Several features of tumor ecosystems, including cellular neighborhoods, were linked to prognosis, illustrating their clinical relevance. In summary, systematic analysis of single-cell phenotypic and spatial correlates of genomic alterations in cancer revealed how genomes shape both the composition and architecture of breast tumor ecosystems and will enable greater understanding of the phenotypic impact of genomic alterations.
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IMC data, including cell masks and processed single-cell data, have been deposited to the Image Data Resource (https://idr.openmicroscopy.org/) under accession code idr0076 (see https://idr.openmicroscopy.org/about/download.html). Previously published METABRIC copy number, gene expression, miRNA and targeted sequencing data that were reanalyzed here are available under accession codes EGAS00000000083, EGAS00000000122 and EGAS00001001753 at the European Genome–Phenome Archive (http://www.ebi.ac.uk/ega/). Updated METABRIC clinical data analyzed here are available as part of the supplementary information in ref. 14. All other data supporting the findings of this study are available from the corresponding authors upon reasonable request.
In-house image preprocessing scripts are available at https://github.com/BodenmillerGroup/imctools. Other analysis code is available from the authors upon request.
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H.R.A. was supported by a Cancer Research UK (CRUK) Clinician Scientist Fellowship. We thank N. De Souza for critical review of the manuscript. The research of B.B. is funded by an SNSF R’Equip grant, an SNSF Assistant Professorship grant, an NIH grant (UC4 DK108132) and by the European Research Council (ERC) under the European Union’s Seventh Framework Program (FP/2007-2013)/ERC grant agreement 336921. The laboratories of B.B. and C.C. were supported by the CRUK IMAXT Grand Challenge for this work.
C.C. is a member of the External Science Panel of AstraZeneca, and his laboratory has received research grants (administered by the University of Cambridge) from Genentech, Roche, AstraZeneca and Servier. The other authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Representative cell masks annotated by protein expression levels (left) and by inferred cell identities separated by tumour versus stroma (right). For protein expression levels, mean counts per cell were normalised relative to all cells analysed. White scale bars (top left) represent 100 µm.
a, Box-and-whisker plot of the distribution of SMA expression by stromal cell types (n = 141, 818 cells). Boxes represent the interquartile range. Lines dividing boxes indicate the median, and vertical lines represent range of expression from the 1st to 99th percentile. b, Pathway enrichment analysis of genes (hypergeometric test; adjusted for multiple comparisons) linked to miRNAs positively correlated with myofibroblast and vascular smooth muscle cell proportions (n = 371 tumours; related to Fig. 4).
a, Stacked bar plot depicting phenotypic composition of cell neighbours separately by each cell phenotype for all tumours. b, Stacked bar plots depicting the phenotypic composition of cells neighbouring all stromal phenotypes separately by IntClust subtype, illustrating patterns of stromal cell enrichment among IntClust subtypes (related to Fig. 4). c, Heatmap of median expression values for stromal cells based on both whole-cell and 3-pixel annular segmentation methods; rows and columns ordered by hierarchical clustering using Ward’s method.
a, Example heatmap of Spearman’s correlation statistics between 100 FlowSOM groups and Phenograph clusters based on median protein expression values, to illustrate the methodology for mapping FlowSOM groups to cell phenotypes assigned using Phenograph. Solid squares indicate largest positive correlations. Rows and columns are ordered by hierarchical clustering using Ward’s method (comparison based on n = 479, 844 cells). b, Bar chart on the left shows the number of cells assigned to the Phenograph cell phenotypes. Bar chart on the right depicts frequency of FlowSOM groups mapped to each Phenograph-clustered phenotypes, arising from 100 runs of FlowSOM each generating 100 groups (10,000 groups mapped in total). This illustrates that most phenotypes were assigned by both methods and that the frequency of mapped groups was related to the number of cells represented by each phenotype. c, Bar charts comparing patterns of association (tested using linear regression) with breast cancer molecular subtypes between mapped cell phenotypes (from 100 runs of FlowSOM each generating 100 groups as in panel b) and the Phenograph-assigned phenotypes. Green and red bars distinguish between enrichment and depletion of a given cell phenotype for each molecular subtype. ‘Original’ on the x-axis indicates associations based on the Phenograph clustering methodology.
Extended Data Fig. 5 Patterns of cell phenotype and cell-cell interaction enrichment among breast cancer molecular subtypes.
a, Patterns of enrichment among metaclusters defined by combining subsets of Phenograph-assigned cell types by descriptive label (for example, fibroblasts, myofibroblasts, T cells). tSNE map on the right indicates position by cell identity (median values for 22 metaclusters computed based on n = 479, 844 cells). Coloured markers indicate significant enrichment. Depicted associations derived from linear regression (n = 390 tumours; two-sided tests; adjusted for multiple comparisons), restricted to those with an adjusted p-value < 0.05, were identified by linear models where the dark grey background is proportional to the derived point estimate, providing an indication of the relative strength of the association. b, Co-occurrence plots of cell-cell interactions identified by permutation testing and found to be significantly enriched (p-value < 0.05 after adjustment for multiple comparisons) among the molecular subtypes indicated (limited to samples that contain both cells for a given interaction; range of n between 86 and 361 tumours for depicted associations). Rows and columns correspond to cell types in the same order as labelled on the y-axis.
tSNE reference maps representing cell types as light grey makers (tSNE map based on median marker expression values derived from n = 479, 844 cells). Neighbourhood enrichment for each cell type within tumour molecular subtypes was determined by fitting a linear model taking mean neighbourhood values as the dependent variable and tumour molecular subtype as independent variable. Coloured markers indicate those significantly enriched within a given subtype (p-value < 0.05). Dark grey background is proportional to the point estimate from the linear model, providing an indication of the strength (size) of the association.
Scatter plots depicting adjusted p-values derived from linear models testing for associations between cell phenotype and genomic alterations (n = 390 tumours; two-sided; adjusted for multiple comparisons). Coloured points represent significant associations (red, gains; blue, losses). Depicted points are restricted to those associated with positive coefficients. Shown are cell phenotypes most affected by copy-number aberrations.
Box and whisker plots of the distributions of cell types as proportions versus quartiles of genomic instability. Boxes represent the interquartile range. Lines dividing boxes indicate the median, and vertical lines represent range of expression from the 1st to 99th percentile. The p-values were derived from two-sided Kruskal-Wallis tests; depicted are those cell phenotypes with a p-value < 0.05 (adjusted for multiple comparisons; n = 404 tumours).
Explained variances (right y-axis) for each of a series of four linear models are depicted as connected circles (n = 357 tumours). Distributions of cell type proportions per tumour (left y-axis) depicted as boxes and whiskers. Boxes represent the interquartile range. Lines dividing boxes indicate the median, and vertical lines represent range of expression from the 1st to 99th percentile.
Stacked bar plot depicting cell phenotype composition per tissue-microarray spot for a subset of fifteen tumours represented by at least two spots. The order of columns was determined using single-linkage hierarchical clustering. Patient IDs are on the x axis. Grey bars highlight where two tissue spots from the same tumour cluster together.
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Ali, H.R., Jackson, H.W., Zanotelli, V.R.T. et al. Imaging mass cytometry and multiplatform genomics define the phenogenomic landscape of breast cancer. Nat Cancer 1, 163–175 (2020). https://doi.org/10.1038/s43018-020-0026-6
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