Detecting repeated cancer evolution from multiregion tumor sequencing data

被引:237
作者
Caravagna, Giulio [1 ,2 ]
Giarratano, Ylenia [2 ,3 ]
Ramazzotti, Daniele [4 ]
Tomlinson, Ian [5 ]
Graham, Trevor A. [6 ]
Sanguinetti, Guido [2 ]
Sottoriva, Andrea [1 ]
机构
[1] Inst Canc Res, Ctr Evolut & Canc, Evolutionary Genom & Modelling Lab, London, England
[2] Univ Edinburgh, Sch Informat, Edinburgh, Midlothian, Scotland
[3] Univ Edinburgh, Usher Inst, Ctr Med Informat, Edinburgh, Midlothian, Scotland
[4] Stanford Univ, Dept Pathol, Stanford, CA 94305 USA
[5] Univ Birmingham, Inst Canc & Genom Sci, Birmingham, W Midlands, England
[6] Queen Mary Univ London, Barts Canc Inst, Ctr Tumour Biol, London, England
基金
英国惠康基金; 美国国家科学基金会;
关键词
INTRATUMOR HETEROGENEITY; STATISTICAL-INFERENCE; LUNG ADENOCARCINOMA; CELL CARCINOMAS; BREAST-TUMORS; GENOME; PROGRESSION; REVEALS; ARCHITECTURE; PATTERNS;
D O I
10.1038/s41592-018-0108-x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recurrent successions of genomic changes, both within and between patients, reflect repeated evolutionary processes that are valuable for the anticipation of cancer progression. Multi-region sequencing allows the temporal order of some genomic changes in a tumor to be inferred, but the robust identification of repeated evolution across patients remains a challenge. We developed a machine-learning method based on transfer learning that allowed us to overcome the stochastic effects of cancer evolution and noise in data and identified hidden evolutionary patterns in cancer cohorts. When applied to multi-region sequencing datasets from lung, breast, renal, and colorectal cancer (768 samples from 178 patients), our method detected repeated evolutionary trajectories in subgroups of patients, which were reproduced in single-sample cohorts (n = 2,935). Our method provides a means of classifying patients on the basis of how their tumor evolved, with implications for the anticipation of disease progression.
引用
收藏
页码:707 / +
页数:11
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