Cell cycle arrest is not yet senescence, which is not just cell cycle arrest: terminology for TOR-driven aging

被引:220
作者
Blagosklonny, Mikhail V. [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Cell Stress Biol, BLSC, Buffalo, NY 14263 USA
来源
AGING-US | 2012年 / 4卷 / 03期
关键词
senescence; geroconversion; gerosuppressants; rapamycin; mTOR; EXTENDS LIFE-SPAN; OXIDATIVE DAMAGE THEORY; INSULIN-RESISTANCE; CAENORHABDITIS-ELEGANS; GROWTH ARREST; C; ELEGANS; AMINO-ACID; P53; MTOR; RAPAMYCIN;
D O I
10.18632/aging.100443
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Cell cycle arrest is not yet senescence. When the cell cycle is arrested, an inappropriate growth-promotion converts an arrest into senescence (geroconversion). By inhibiting the growth-promoting mTOR pathway, rapamycin decelerates geroconversion of the arrested cells. And as a striking example, while causing arrest, p53 may decelerate or suppress geroconversion (in some conditions). Here I discuss the meaning of geroconversion and also the terms gerogenes, gerossuppressors, gerosuppressants, gerogenic pathways, gero-promoters, hyperfunction and feedback resistance, regenerative potential, hypertrophy and secondary atrophy, pro-gerogenic and gerogenic cells.
引用
收藏
页码:159 / 165
页数:7
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