Rapamycin and quasi-programmed aging Four years later

被引:87
作者
Blagosklonny, Mikhail V. [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA
关键词
aging; senescence; aging-suppression; rapamycin; mTOR; LIFE-SPAN EXTENSION; CELLULAR SENESCENCE; DIETARY RESTRICTION; S6; KINASE; MTOR; GROWTH; DAMAGE; OVEREXPRESSION; INHIBITION; ARREST;
D O I
10.4161/cc.9.10.11872
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In 2006, Cell Cycle featured the concept that aging is not caused by molecular damage (nor by free radicals) but instead is a purposeless quasi-program (program-like, but not a program) driven in part by TOR (Target of Rapamycin). Taken together with the analysis of clinical data, this pointed to Sirolimus (rapamycin) as a genuine anti-aging drug which will prolong life in humans and prevent age-related diseases by slowing down aging. Since that time many predictions of this concept have been confirmed. Rapamycin was shown to suppress aging in mammalian cells, prolong life span in mice and flies, improve immunity and stem cell function in old animals, thus confirming twelve predictions as discussed herein. One prediction remains to be confirmed: rapamycin will become the cornerstone of anti-aging therapy in our life time.
引用
收藏
页码:1859 / 1862
页数:4
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