Cell division rates decrease with age, providing a potential explanation for the age-dependent deceleration in cancer incidence Journal Article


Authors: Tomasetti, C.; Poling, J.; Roberts, N. J.; London, N. R. Jr; Pittman, M. E.; Haffner, M. C.; Rizzo, A.; Baras, A.; Karim, B.; Kim, A.; Heaphy, C. M.; Meeker, A. K.; Hruban, R. H.; Iacobuzio-Donahue, C. A.; Vogelstein, B.
Article Title: Cell division rates decrease with age, providing a potential explanation for the age-dependent deceleration in cancer incidence
Abstract: A new evaluation of previously published data suggested to us that the accumulation of mutations might slow, rather than increase, as individuals age. To explain this unexpected finding, we hypothesized that normal stem cell division rates might decrease as we age. To test this hypothesis, we evaluated cell division rates in the epithelium of human colonic, duodenal, esophageal, and posterior ethmoid sinonasal tissues. In all 4 tissues, there was a significant decrease in cell division rates with age. In contrast, cell division rates did not decrease in the colon of aged mice, and only small decreases were observed in their small intestine or esophagus. These results have important implications for understanding the relationship between normal stem cells, aging, and cancer. Moreover, they provide a plausible explanation for the enigmatic age-dependent deceleration in cancer incidence in very old humans but not in mice. © 2019 National Academy of Sciences. All rights reserved.
Keywords: controlled study; aged; nonhuman; cancer incidence; animal cell; mouse; cell division; animal experiment; stem cell; aging; mutation rate; epithelium; small intestine; colon; esophagus; ethmoid bone; cancer; article; deceleration
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 116
Issue: 41
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2019-10-08
Start Page: 20482
End Page: 20488
Language: English
DOI: 10.1073/pnas.1905722116
PUBMED: 31548407
PROVIDER: scopus
PMCID: PMC6789572
DOI/URL:
Notes: Article -- Export Date: 1 November 2019 -- Source: Scopus
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