Targeting the biology of aging with mTOR inhibitors

被引:162
作者
Mannick, Joan B. [1 ]
Lamming, Dudley W. [2 ]
机构
[1] Tornado Therapeut, New York, NY USA
[2] Univ Wisconsin Madison, Dept Med, Madison, WI 53706 USA
来源
NATURE AGING | 2023年 / 3卷 / 06期
关键词
EXTENDS LIFE-SPAN; TRANSFER-RNA SYNTHETASE; (LRS)-TARGETED MAMMALIAN TARGET; HEMATOPOIETIC STEM-CELLS; TERM CALORIC RESTRICTION; MOUSE MODEL; AMINO-ACID; RAPAMYCIN TREATMENT; INSULIN-RESISTANCE; PROTEIN-SYNTHESIS;
D O I
10.1038/s43587-023-00416-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lamming and Mannick discuss work over the past decade showing that rapamycin promotes survival in multiple species and how recent clinical trials have finally begun to explore whether existing mTOR inhibitors can safely prevent, delay or treat multiple diseases of aging in humans. Inhibition of the protein kinase mechanistic target of rapamycin (mTOR) with the Food and Drug Administration (FDA)-approved therapeutic rapamycin promotes health and longevity in diverse model organisms. More recently, specific inhibition of mTORC1 to treat aging-related conditions has become the goal of basic and translational scientists, clinicians and biotechnology companies. Here, we review the effects of rapamycin on the longevity and survival of both wild-type mice and mouse models of human diseases. We discuss recent clinical trials that have explored whether existing mTOR inhibitors can safely prevent, delay or treat multiple diseases of aging. Finally, we discuss how new molecules may provide routes to the safer and more selective inhibition of mTOR complex 1 (mTORC1) in the decade ahead. We conclude by discussing what work remains to be done and the questions that will need to be addressed to make mTOR inhibitors part of the standard of care for diseases of aging.
引用
收藏
页码:642 / 660
页数:19
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