mTOR Signaling Pathway and mTOR Inhibitors in Cancer Therapy

被引:107
作者
Gomez-Pinillos, Alejandro [1 ]
Ferrari, Anna C. [1 ]
机构
[1] NYU, Sch Med, NYU Canc Inst, Dept Med, New York, NY 10016 USA
关键词
mTOR; Inhibitor; Rapalog; Cancer; RENAL-CELL CARCINOMA; GROWTH-FACTOR RECEPTOR; ORAL MAMMALIAN TARGET; PHASE-II TRIAL; MET PROTOONCOGENE EXPRESSION; SINGLE-AGENT TEMSIROLIMUS; ACTIVATED PROTEIN-KINASES; PTEN GENOMIC DELETION; K-RAS MUTATIONS; TUMOR-SUPPRESSOR;
D O I
10.1016/j.hoc.2012.02.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mammalian target of rapamycin (mTOR) is a serine/threonine protein kinase. It is ubiquitously expressed in cells and is a therapeutic target for the cancer treatment arsenal. Despite the great responses obtained in tumors addicted to specific mutations or overactivation of key members of the mTOR pathway (HiF1 alpha in RCC, cyclin D1 in MCL, or TSC in SEGA), mTOR inhibitors as single agents have modest activity. Dual PI3K/mTOR kinase inhibitors have been developed with the idea of overcoming resistance to the mTOR inhibition through preventing the activation of PI3K/Akt as a result of release negative feedback loops.
引用
收藏
页码:483 / +
页数:24
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