Reconstructing tumor evolutionary histories and clone trees in polynomial-time with SubMARine

Tumors contain multiple subpopulations of genetically distinct cancer cells. Reconstructing their evolutionary history can improve our understanding of how cancers develop and respond to treatment. Subclonal reconstruction methods cluster mutations into groups that co-occur within the same subpopulations, estimate the frequency of cells belonging to each subpopulation, and infer the ancestral relationships among the subpopulations by constructing a clone tree. However, often multiple clone trees are consistent with the data and current methods do not efficiently capture this uncertainty; nor can these methods scale to clone trees with a large number of subclonal populations. Here, we formalize the notion of a partially-defined clone tree (partial clone tree for short) that defines a subset of the pairwise ancestral relationships in a clone tree, thereby implicitly representing the set of all clone trees that have these defined pairwise relationships. Also, we introduce a special partial clone tree, the Maximally-Constrained Ancestral Reconstruction (MAR), which summarizes all clone trees fitting the input data equally well. Finally, we extend commonly used clone tree validity conditions to apply to partial clone trees and describe SubMARine, a polynomial-time algorithm producing the subMAR, which approximates the MAR and guarantees that its defined relationships are a subset of those present in the MAR. We also extend SubMARine to work with subclonal copy number aberrations and define equivalence constraints for this purpose. Further, we extend SubMARine to permit noise in the estimates of the subclonal frequencies while retaining its validity conditions and guarantees. In contrast to other clone tree reconstruction methods, SubMARine runs in time and space that scale polynomially in the number of subclones. We show through extensive noise-free simulation, a large lung cancer dataset and a prostate cancer dataset that the subMAR equals the MAR in all cases where only a single clone tree exists and that it is a perfect match to the MAR in most of the other cases. Notably, SubMARine runs in less than 70 seconds on a single thread with less than one Gb of memory on all datasets presented in this paper, including ones with 50 nodes in a clone tree. On the real-world data, SubMARine almost perfectly recovers the previously reported trees and identifies minor errors made in the expert-driven reconstructions of those trees. The freely-available open-source code implementing SubMARine can be downloaded at https://github.com/morrislab/submarine.

[1]  Daniel Q. Naiman,et al.  SubClonal Hierarchy Inference from Somatic Mutations: Automatic Reconstruction of Cancer Evolutionary Trees from Multi-region Next Generation Sequencing , 2015, bioRxiv.

[2]  Benjamin J. Raphael,et al.  THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data , 2013, Genome Biology.

[3]  Nathan M. Wilson,et al.  A community effort to create standards for evaluating tumor subclonal reconstruction , 2019, Nature Biotechnology.

[4]  Benjamin J. Raphael,et al.  Inferring the Mutational History of a Tumor Using Multi-state Perfect Phylogeny Mixtures. , 2016, Cell systems.

[5]  Benjamin J. Raphael,et al.  Tumor phylogeny inference using tree-constrained importance sampling , 2017, Bioinform..

[6]  Shibu Yooseph,et al.  Haplotyping as Perfect Phylogeny: A Direct Approach , 2003, J. Comput. Biol..

[7]  P. A. Futreal,et al.  Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. , 2012, The New England journal of medicine.

[8]  Joshua F. McMichael,et al.  Clonal evolution in relapsed acute myeloid leukemia revealed by whole genome sequencing , 2011, Nature.

[9]  Mohammed El-Kebir,et al.  Implications of non-uniqueness in phylogenetic deconvolution of bulk DNA samples of tumors , 2019, Algorithms for Molecular Biology.

[10]  Jenny Taylor,et al.  Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns. , 2012, Blood.

[11]  R. Karp,et al.  Efficient reconstruction of haplotype structure via perfect phylogeny. , 2002, Journal of bioinformatics and computational biology.

[12]  Hanlee P. Ji,et al.  Pan-cancer analysis of the extent and consequences of intratumor heterogeneity , 2015, Nature Medicine.

[13]  Iman Hajirasouliha,et al.  Fast and scalable inference of multi-sample cancer lineages , 2014, Genome Biology.

[14]  G. Parmigiani,et al.  Heterogeneity of genomic evolution and mutational profiles in multiple myeloma , 2014, Nature Communications.

[15]  David C Wedge,et al.  Principles of Reconstructing the Subclonal Architecture of Cancers. , 2017, Cold Spring Harbor perspectives in medicine.

[16]  F. Markowetz,et al.  The evolutionary history of 2,658 cancers , 2017, bioRxiv.

[17]  A. Børresen-Dale,et al.  The Life History of 21 Breast Cancers , 2012, Cell.

[18]  Christopher J. R. Illingworth,et al.  High-Definition Reconstruction of Clonal Composition in Cancer , 2014, Cell reports.

[19]  Ali Bashashati,et al.  Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer , 2016, Nature Genetics.

[20]  Nancy R. Zhang,et al.  Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencing , 2016, Proceedings of the National Academy of Sciences.

[21]  Mohammed El-Kebir,et al.  Summarizing the solution space in tumor phylogeny inference by multiple consensus trees , 2019, Bioinform..

[22]  Franziska Michor,et al.  Myeloma Cell Dynamics in Response to Treatment Supports a Model of Hierarchical Differentiation and Clonal Evolution , 2016, Clinical Cancer Research.

[23]  S. Blagden,et al.  Harnessing Pandemonium: The Clinical Implications of Tumor Heterogeneity in Ovarian Cancer , 2015, Front. Oncol..

[24]  Andrew Menzies,et al.  The patterns and dynamics of genomic instability in metastatic pancreatic cancer , 2010, Nature.

[25]  Nancy R. Zhang,et al.  Allele-specific copy number profiling by next-generation DNA sequencing , 2014, Nucleic acids research.

[26]  Junfeng Wang,et al.  Inferring Clonal Composition from Multiple Sections of a Breast Cancer , 2014, PLoS Comput. Biol..

[27]  Obi L. Griffith,et al.  SciClone: Inferring Clonal Architecture and Tracking the Spatial and Temporal Patterns of Tumor Evolution , 2014, PLoS Comput. Biol..

[28]  Nicolai J. Birkbak,et al.  Tracking the Evolution of Non‐Small‐Cell Lung Cancer , 2017, The New England journal of medicine.

[29]  Benjamin J. Raphael,et al.  Reconstruction of clonal trees and tumor composition from multi-sample sequencing data , 2015, Bioinform..

[30]  Shankar Vembu,et al.  PhyloWGS: Reconstructing subclonal composition and evolution from whole-genome sequencing of tumors , 2015, Genome Biology.

[31]  Sohrab P. Shah,et al.  TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data , 2014, Genome research.

[32]  Benjamin J. Raphael,et al.  Accurate quantification of copy-number aberrations and whole-genome duplications in multi-sample tumor sequencing data , 2020, Nature communications.

[33]  Nilgun Donmez,et al.  Clonality inference in multiple tumor samples using phylogeny , 2015, Bioinform..

[34]  Y. Kluger,et al.  TrAp: a tree approach for fingerprinting subclonal tumor composition , 2013, Nucleic acids research.

[35]  Jack Kuipers,et al.  Single-cell sequencing data reveal widespread recurrence and loss of mutational hits in the life histories of tumors , 2017, Genome research.

[36]  Eugene W. Myers,et al.  Finding All Spanning Trees of Directed and Undirected Graphs , 1978, SIAM J. Comput..

[37]  Shankar Vembu,et al.  Inferring clonal evolution of tumors from single nucleotide somatic mutations , 2012, BMC Bioinformatics.

[38]  Mark Cobbold,et al.  Tracking Genomic Cancer Evolution for Precision Medicine: The Lung TRACERx Study , 2014, PLoS biology.

[39]  Iman Hajirasouliha,et al.  A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data , 2014, Bioinform..

[40]  A. Bouchard-Côté,et al.  PyClone: statistical inference of clonal population structure in cancer , 2014, Nature Methods.

[41]  M. Nykter,et al.  The Evolutionary History of Lethal Metastatic Prostate Cancer , 2015, Nature.

[42]  Z. Szallasi,et al.  Sequenza: allele-specific copy number and mutation profiles from tumor sequencing data , 2014, Annals of oncology : official journal of the European Society for Medical Oncology.