mTORC1型
mTORC2型
西罗莫司
PI3K/AKT/mTOR通路
雷帕霉素的作用靶点
药理学
长寿
生物
信号转导
细胞生物学
遗传学
生物化学
作者
Sebastian I. Arriola Apelo,Dudley W. Lamming
出处
期刊:The Journals of Gerontology
[Oxford University Press]
日期:2016-05-21
卷期号:71 (7): 841-849
被引量:168
标识
DOI:10.1093/gerona/glw090
摘要
Rapamycin (sirolimus) is a macrolide immunosuppressant that inhibits the mechanistic target of rapamycin (mTOR) protein kinase and extends lifespan in model organisms including mice. Although rapamycin is an FDA-approved drug for select indications, a diverse set of negative side effects may preclude its wide-scale deployment as an antiaging therapy. mTOR forms two different protein complexes, mTORC1 and mTORC2; the former is acutely sensitive to rapamycin whereas the latter is only chronically sensitive to rapamycin in vivo. Over the past decade, it has become clear that although genetic and pharmacological inhibition of mTORC1 extends lifespan and delays aging, inhibition of mTORC2 has negative effects on mammalian health and longevity and is responsible for many of the negative side effects of rapamycin. In this review, we discuss recent advances in understanding the molecular and physiological effects of rapamycin treatment, and we discuss how the use of alternative rapamycin treatment regimens or rapamycin analogs has the potential to mitigate the deleterious side effects of rapamycin treatment by more specifically targeting mTORC1. Although the side effects of rapamycin are still of significant concern, rapid progress is being made in realizing the revolutionary potential of rapamycin-based therapies for the treatment of diseases of aging.
科研通智能强力驱动
Strongly Powered by AbleSci AI