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Targeting the biology of aging with mTOR inhibitors

Journal

NATURE AGING
Volume 3, Issue 6, Pages 642-660

Publisher

SPRINGERNATURE
DOI: 10.1038/s43587-023-00416-y

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Lamming and Mannick discuss the research in the past decade showing the survival-promoting effects of rapamycin in multiple species and the recent clinical trials exploring the use of existing mTOR inhibitors in preventing, delaying or treating aging-related diseases in humans.
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.

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