西罗莫司
PI3K/AKT/mTOR通路
自噬
mTORC1型
血管生成
药理学
生物
癌症研究
医学
信号转导
细胞生物学
内科学
遗传学
细胞凋亡
作者
Christine Hartford,Mark J. Ratain
标识
DOI:10.1038/sj.clpt.6100317
摘要
The molecular target of rapamycin (mTOR) is central to a complex intracellular signaling pathway and is involved in diverse processes including cell growth and proliferation, angiogenesis, autophagy, and metabolism. Although sirolimus (rapamycin), the oldest inhibitor of mTOR, was discovered more than 30 years ago, renewed interest in this pathway is evident by the numerous rapalogs recently developed. These newer agents borrow from the structure of sirolimus and, although there are some pharmacokinetic differences, they appear to differ little in terms of pharmacodynamic effects and overall tolerability. Given the multitude of potential applications for this class of agents and the decrease in cost that can be expected upon the expiration of sirolimus patents, renewed focus on this agent is warranted. Clinical Pharmacology & Therapeutics (2007) 82, 381–388. doi:10.1038/sj.clpt.6100317; published online 29 August 2007
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