The life history of 21 breast cancers

S. Nik-Zainal, P. Van Loo, D.C. Wedge, L.B. Alexandrov, C.D. Greenman, K.W. Lau, K. Raine, D. Jones, J. Marshall, M. Ramakrishna, A. Shlien, S.L. Cooke, J. Hinton, A. Menzies, L.A. Stebbings, C. Leroy, M. Jia, R. Rance, L.J. Mudie, S.J. GambleP.J. Stephens, S. McLaren, P.S. Tarpey, E. Papaemmanuil, H.R. Davies, I. Varela, D.J. McBride, G.R. Bignell, K. Leung, A.P. Butler, J.W. Teague, S. Martin, G. Jönsson, O. Mariani, S. Boyault, P. Miron, A. Fatima, A. Langerod, S.A.J.R. Aparicio, A. Tutt, A.M. Sieuwerts, Å. Borg, G. Thomas, A.V. Salomon, A.L. Richardson, A.-L. Borresen-Dale, P.A. Futreal, M.R. Stratton, P.J. Campbell

Research output: Contribution to journalArticlepeer-review


Cancer evolves dynamically as clonal expansions supersede one another driven by shifting selective pressures, mutational processes, and disrupted cancer genes. These processes mark the genome, such that a cancer's life history is encrypted in the somatic mutations present. We developed algorithms to decipher this narrative and applied them to 21 breast cancers. Mutational processes evolve across a cancer's lifespan, with many emerging late but contributing extensive genetic variation. Subclonal diversification is prominent, and most mutations are found in just a fraction of tumor cells. Every tumor has a dominant subclonal lineage, representing more than 50% of tumor cells. Minimal expansion of these subclones occurs until many hundreds to thousands of mutations have accumulated, implying the existence of long-lived, quiescent cell lineages capable of substantial proliferation upon acquisition of enabling genomic changes. Expansion of the dominant subclone to an appreciable mass may therefore represent the final rate-limiting step in a breast cancer's development, triggering diagnosis.
Original languageEnglish
Pages (from-to)994-1007
Number of pages14
Issue number5
Publication statusPublished - 25 May 2012

Research Beacons, Institutes and Platforms

  • Manchester Cancer Research Centre


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