Quantitative measurement of phenotype dynamics during cancer drug resistance evolution using genetic barcoding

Cancer treatment frequently fails due to the evolution of drug-resistant cell phenotypes driven by genetic or non-genetic changes. The origin, timing, and rate of spread of these adaptations are critical for understanding drug resistance mechanisms but remain challenging to observe directly. We present a mathematical framework to infer drug resistance dynamics from genetic lineage tracing and population size data without direct measurement of resistance phenotypes. Simulation experiments demonstrate that the framework accurately recovers ground-truth evolutionary dynamics. Experimental evolution to 5-Fu chemotherapy in colorectal cancer cell lines SW620 and HCT116 validates the framework. In SW620 cells, a stable pre-existing resistant subpopulation was inferred, whereas in HCT116 cells, resistance emerged through phenotypic switching into a slow-growing resistant state with stochastic progression to full resistance. Functional assays, including scRNA-seq and scDNA-seq, validate these distinct evolutionary routes. This framework facilitates rapid characterisation of resistance mechanisms across diverse experimental settings.

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Publication Details

Journal
Nature Communications
Published
2025-06-20
DOI
https://doi.org/10.1038/s41467-025-59479-7
Citations
4
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
3.75

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article

Quantitative measurement of phenotype dynamics during cancer drug resistance evolution using genetic barcoding

Richard A. Nichols, C. Barnes, Trevor A. Graham, Andrea Sottoriva et al.
4 citations
Nature Communications
Cancer Genomics and Diagnostics
3.75
article

Quantitative measurement of phenotype dynamics during cancer drug resistance evolution using genetic barcoding

Richard A. Nichols, C. Barnes, Trevor A. Graham, Andrea Sottoriva, Ann‐Marie Baker, Erika Yara-Romero, Christopher Kimberley, Maximilian Mossner, Calum Gabbutt, Frederick J.H. Whiting
article en
4 citations

Abstract

Cancer treatment frequently fails due to the evolution of drug-resistant cell phenotypes driven by genetic or non-genetic changes. The origin, timing, and rate of spread of these adaptations are critical for understanding drug resistance mechanisms but remain challenging to observe directly. We present a mathematical framework to infer drug resistance dynamics from genetic lineage tracing and population size data without direct measurement of resistance phenotypes. Simulation experiments demonstrate that the framework accurately recovers ground-truth evolutionary dynamics. Experimental evolution to 5-Fu chemotherapy in colorectal cancer cell lines SW620 and HCT116 validates the framework. In SW620 cells, a stable pre-existing resistant subpopulation was inferred, whereas in HCT116 cells, resistance emerged through phenotypic switching into a slow-growing resistant state with stochastic progression to full resistance. Functional assays, including scRNA-seq and scDNA-seq, validate these distinct evolutionary routes. This framework facilitates rapid characterisation of resistance mechanisms across diverse experimental settings.

Nature CommunicationsVol. 16(1)
Institute of Cancer Research (GB), Queen Mary University of London (GB), MRC Laboratory for Molecular Cell Biology (GB), NIHR Imperial Biomedical Research Centre (GB), Human Technopole (IT), University College London (GB), Imperial College London (GB)
Wellcome, Cancer Research UK
Good health and well-being
Openalex Percentile: Top 7%
Cancer Genomics and Diagnostics
3.75
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