Comparative lesion sequencing provides insights into tumor evolution

Siân Jones(Howard Hughes Medical Institute), Wei-Dong Chen(Howard Hughes Medical Institute), Giovanni Parmigiani(Howard Hughes Medical Institute), Frank Diehl(Howard Hughes Medical Institute), Niko Beerenwinkel(Harvard University), Tibor Antal(Harvard University), Arne Traulsen(Harvard University), Martin A. Nowak(Harvard University), Christopher Siegel, Victor E. Velculescu(Howard Hughes Medical Institute), Kenneth W. Kinzler(Howard Hughes Medical Institute), Bert Vogelstein(Howard Hughes Medical Institute), Joseph Willis(University Hospitals of Cleveland), Sanford D. Markowitz(Howard Hughes Medical Institute)
Proceedings of the National Academy of Sciences
March 12, 2008
Cited by 830Open Access
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Abstract

We show that the times separating the birth of benign, invasive, and metastatic tumor cells can be determined by analysis of the mutations they have in common. When combined with prior clinical observations, these analyses suggest the following general conclusions about colorectal tumorigenesis: (i) It takes approximately 17 years for a large benign tumor to evolve into an advanced cancer but <2 years for cells within that cancer to acquire the ability to metastasize; (ii) it requires few, if any, selective events to transform a highly invasive cancer cell into one with the capacity to metastasize; (iii) the process of cell culture ex vivo does not introduce new clonal mutations into colorectal tumor cell populations; and (iv) the rates at which point mutations develop in advanced cancers are similar to those of normal cells. These results have important implications for understanding human tumor pathogenesis, particularly those associated with metastasis.


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