Delayed ageing through damage protection by the Arf/p53 pathway

被引:360
作者
Matheu, Ander
Maraver, Antonio
Klatt, Peter
Flores, Ignacio
Garcia-Cao, Isabel
Borras, Consuelo
Flores, Juana M.
Vina, Jose
Blasco, Maria A.
Serrano, Manuel [1 ]
机构
[1] Spanish Natl Canc Res Ctr CNIO, Tumor Suppress Grp, Madrid 28029, Spain
[2] Spanish Natl Canc Res Ctr CNIO, Telomeres & Telomerase Grp, Madrid 28029, Spain
[3] Univ Valencia, Dept Physiol, Valencia 46010, Spain
[4] Univ Complutense Madrid, Dept Anim Surg & Med, E-28040 Madrid, Spain
关键词
D O I
10.1038/nature05949
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The tumour-suppressor pathway formed by the alternative reading frame protein of the Cdkn2a locus (Arf) and by p53 (also called Trp53) plays a central part in the detection and elimination of cellular damage, and this constitutes the basis of its potent cancer protection activity(1,2). Similar to cancer, ageing also results from the accumulation of damage and, therefore, we have reasoned that Arf/p53 could have anti-ageing activity by alleviating the load of age-associated damage. Here we show that genetically manipulated mice with increased, but otherwise normally regulated, levels of Arf and p53 present strong cancer resistance and have decreased levels of ageing-associated damage. These observations extend the protective role of Arf/p53 to ageing, revealing a previously unknown anti-ageing mechanism and providing a rationale for the co-evolution of cancer resistance and longevity.
引用
收藏
页码:375 / U14
页数:6
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