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Substantial contribution of extrinsic risk factors to cancer development.
Wu, Song; Powers, Scott; Zhu, Wei; Hannun, Yusuf A.
Affiliation
  • Wu S; Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, New York 11794, USA.
  • Powers S; Stony Brook Cancer Center, Stony Brook University, Health Sciences Center, Stony Brook, New York 11794, USA.
  • Zhu W; Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, New York 11794, USA.
  • Hannun YA; Stony Brook Cancer Center, Stony Brook University, Health Sciences Center, Stony Brook, New York 11794, USA.
Nature ; 529(7584): 43-7, 2016 Jan 07.
Article in En | MEDLINE | ID: mdl-26675728
ABSTRACT
Recent research has highlighted a strong correlation between tissue-specific cancer risk and the lifetime number of tissue-specific stem-cell divisions. Whether such correlation implies a high unavoidable intrinsic cancer risk has become a key public health debate with the dissemination of the 'bad luck' hypothesis. Here we provide evidence that intrinsic risk factors contribute only modestly (less than ~10-30% of lifetime risk) to cancer development. First, we demonstrate that the correlation between stem-cell division and cancer risk does not distinguish between the effects of intrinsic and extrinsic factors. We then show that intrinsic risk is better estimated by the lower bound risk controlling for total stem-cell divisions. Finally, we show that the rates of endogenous mutation accumulation by intrinsic processes are not sufficient to account for the observed cancer risks. Collectively, we conclude that cancer risk is heavily influenced by extrinsic factors. These results are important for strategizing cancer prevention, research and public health.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Self Renewal / Models, Biological / Neoplasms Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nature Year: 2016 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Cell Self Renewal / Models, Biological / Neoplasms Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nature Year: 2016 Type: Article Affiliation country: United States