Quantifying cell divisions along evolutionary lineages in cancer

Martin Blohmer, David M. Cheek, Wei Ting Hung, Maria Kessler, Foivos Chatzidimitriou, Jiahe Wang, William Hung, I. Hsiu Lee, Alexander N. Gorelick, Emma C.E. Wassenaar, Ching Yeuh Yang, Yi Chen Yeh, Hsiang Ling Ho, Dorothee Speiser, Maria M. Karsten, Michael Lanuti, Sara I. Pai, Onno Kranenburg, Jochen K. Lennerz, Teh Ying ChouMatthias Kloor, Kamila Naxerova*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Cell division drives somatic evolution but is challenging to quantify. We developed a framework to count cell divisions with DNA replication-related mutations in polyguanine homopolymers. Analyzing 505 samples from 37 patients, we studied the milestones of colorectal cancer evolution. Primary tumors diversify at ~250 divisions from the founder cell, while distant metastasis divergence occurs significantly later, at ~500 divisions. Notably, distant but not lymph node metastases originate from primary tumor regions that have undergone surplus divisions, tying subclonal expansion to metastatic capacity. Then, we analyzed a cohort of 73 multifocal lung cancers and showed that the cell division burden of the tumors’ common ancestor distinguishes independent primary tumors from intrapulmonary metastases and correlates with patient survival. In lung cancer too, metastatic capacity is tied to more extensive proliferation. The cell division history of human cancers is easily accessible using our simple framework and contains valuable biological and clinical information.

Original languageEnglish
Pages (from-to)706–717
Number of pages12
JournalNature genetics
Volume57
Issue number3
Early online date4 Feb 2025
DOIs
Publication statusPublished - Mar 2025

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