Declining p53 function in the aging process: A possible mechanism for the increased tumor incidence in older populations Journal Article


Authors: Feng, Z.; Hu, W.; Teresky, A. K.; Hernando, E.; Cordon-Cardo, C.; Levine, A. J.
Article Title: Declining p53 function in the aging process: A possible mechanism for the increased tumor incidence in older populations
Abstract: Cancer is a disease of aging. The accumulation of mutations in individual cells over a lifetime is thought to be the reason. In this work, we explored an additional hypothesis: could p53 function decline with age, which would contribute to an enhanced mutation frequency and tumorigenesis in the aging process? The efficiency of the p53 response to γ-irradiation was found to decline significantly in various tissues of aging mice from several inbred strains, including lower p53 transcriptional activity and p53-dependent apoptosis. This decline resulted from a decreased stabilization of the p53 protein after stress. The function of the Ataxia-telangiectasia mutated (ATM) kinase declined significantly with age, which may then be responsible for the decline of the p53 response to radiation. Declining p53 responses to other stresses were also observed in the cultured splenocytes from aging mice. Interestingly, the time of onset of this decreased p53 response correlated with the life span of mice; mice that live longer delay their onset of decreased p53 activity with time. These results suggest an enhanced fixation of mutations in older individuals because of the declining fidelity of p53-mediated apoptosis or senescence in response to stress, and they suggest a plausible explanation for the correlation between tumorigenesis and the aging process. © 2007 by The National Academy of Sciences of the USA.
Keywords: controlled study; gene mutation; mutation; dna-binding proteins; nonhuman; cancer incidence; protein function; neoplasms; animal cell; mouse; animals; cell cycle proteins; mice; animal tissue; mus; apoptosis; animal experiment; gene frequency; transcription, genetic; protein p53; carcinogenesis; tumorigenesis; protein-serine-threonine kinases; tumor suppressor proteins; atm protein; tumor suppressor protein p53; gamma irradiation; aging; mutagenesis; ataxia telangiectasia; ataxia-telangiectasia mutated (atm); cheirogaleidae
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 104
Issue: 42
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2007-10-16
Start Page: 16633
End Page: 16638
Language: English
DOI: 10.1073/pnas.0708043104
PUBMED: 17921246
PROVIDER: scopus
PMCID: PMC2034252
DOI/URL:
Notes: --- - "Cited By (since 1996): 57" - "Export Date: 17 November 2011" - "CODEN: PNASA" - "Source: Scopus"
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