PI3K/AKT/mTOR通路
mTOR抑制剂的发现与发展
医学
癌症研究
药理学
癌症
替西罗莫司
依维莫司
蛋白激酶B
细胞凋亡
化学
肿瘤科
内科学
生物化学
作者
Xianbo Wu,Yihua Xu,Qi Liang,Xinwei Yang,Jianli Huang,Jie Wang,Hong Zhang,Jianyou Shi
标识
DOI:10.3389/fphar.2022.875372
摘要
The PI3K-Akt-mTOR pathway is a viable target for cancer treatment and can be used to treat various malignant tumours, including follicular lymphoma and breast cancer. Both enzymes, PI3K and mTOR, are critical in this pathway. Hence, in recent years, an array of inhibitors targeting these two targets have been studied, showing dual PI3K/mTOR inhibition compared with single targeting small molecule inhibitors. Inhibitors not only inhibit cell proliferation but also promote cell apoptosis. These inhibitors show high potency and little drug resistance even at low doses, suggesting that PI3K/mTOR inhibitors are promising cancer drugs. Herein, we summarised the recent research of PI3K/mTOR dual inhibitors-for example, structure-activity relationship, pharmacokinetics, and clinical practice, and briefly commented on them. Clinical Trial Registration: https://clinicaltrials.gov.
科研通智能强力驱动
Strongly Powered by AbleSci AI