PI3K/AKT/mTOR通路
雷帕霉素的作用靶点
mTOR抑制剂的发现与发展
变构调节
医学
RPTOR公司
激酶
西罗莫司
mTORC2型
药品
药理学
药物发现
癌症研究
mTORC1型
化学
生物
信号转导
细胞生物学
生物信息学
生物化学
酶
作者
Don Benjamin,Marco Colombi,Christoph Moroni,Michael N. Hall
摘要
Mammalian target of rapamycin (mTOR) is an atypical protein kinase that controls growth and metabolism in response to nutrients, growth factors and cellular energy levels, and it is frequently dysregulated in cancer and metabolic disorders. Rapamycin is an allosteric inhibitor of mTOR, and was approved as an immuno-suppressant in 1999. In recent years, interest has focused on its potential as an anticancer drug. However, the performance of rapamycin and its analogues (rapalogues) has been undistinguished despite isolated successes in subsets of cancer, suggesting that the full therapeutic potential of targeting mTOR has yet to be exploited. A new generation of ATP-competitive inhibitors that directly target the mTOR catalytic site display potent and comprehensive mTOR inhibition and are in early clinical trials.
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