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Mutations That Increase the Life Span of C. elegans Inhibit Tumor Growth
Julie M. Pinkston,
Delia Garigan,
Malene Hansen,
Cynthia Kenyon*
Abstract:
Mutations in gld-1 cause lethal germline tumors in the nematodeCaenorhabditis elegans. We find that a wide variety of mutationsthat extend C. elegans' life span confer resistance to thesetumors. The long life spans of daf-2/insulin-receptor mutantswere not shortened at all by gld-1 mutations; we attribute thisfinding to decreased cell division and increased DAF-16/p53dependentapoptosis within the tumors. Mutations that increase life spanby restricting food intake or inhibiting respiration did notaffect apoptosis but reduced tumor cell division. Unexpectedly,none of these longevity mutations affected mitosis in normalgermlines; this finding suggests that cellular changes thatlead to longevity preferentially antagonize tumor cell growth.
Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158, USA.
* To whom correspondence should be addressed. E-mail: ckenyon{at}biochem.ucsf.edu
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