Next-generation mTOR inhibitors in clinical oncology: how pathway complexity informs therapeutic strategy

被引:351
作者
Wander, Seth A. [1 ,2 ]
Hennessy, Bryan T. [3 ,4 ]
Slingerland, Joyce M. [1 ,5 ,6 ]
机构
[1] Univ Miami, Miller Sch Med, BFBCI, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Grad Program Canc Biol, Miami, FL 33136 USA
[3] Beaumont Hosp, Dublin 9, Ireland
[4] Royal Coll Surgeons Ireland, Dublin 2, Ireland
[5] Univ Miami, Miller Sch Med, Dept Med, Miami, FL 33136 USA
[6] Univ Miami, Miller Sch Med, Dept Biochem & Mol Biol, Miami, FL 33136 USA
关键词
PHOSPHATIDYLINOSITOL 3-KINASE/MAMMALIAN TARGET; PHASE-II TRIAL; TUBEROUS SCLEROSIS COMPLEX; RAPAMYCIN KINASE INHIBITOR; SINGLE-AGENT TEMSIROLIMUS; DUAL PI3K/MTOR INHIBITOR; BREAST-CANCER CELLS; ATP-CITRATE LYASE; MAMMALIAN TARGET; P27(KIP1) PHOSPHORYLATION;
D O I
10.1172/JCI44145
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mammalian target of rapamycin (mTOR) is a PI3K-related kinase that regulates cell growth, proliferation, and survival via mTOR complex 1 (mTORC1) and mTORC2. The mTOR pathway is often aberrantly activated in cancers. While hypoxia, nutrient deprivation, and DNA damage restrain mTORC1 activity, multiple genetic events constitutively activate mTOR in cancers. Here we provide a brief overview of the signaling pathways up- and downstream of mTORC1 and -2, and discuss the insights into therapeutic anticancer targets - both those that have been tried in the clinic with limited success and those currently under clinical development - that knowledge of these pathways gives us.
引用
收藏
页码:1231 / 1241
页数:11
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