The mTOR Pathway: A New Target in Cancer Therapy

被引:150
作者
Ciuffreda, L. [1 ]
Di Sanza, C. [1 ]
Incani, U. C. [1 ]
Milella, M. [1 ]
机构
[1] Regina Elena Inst Canc Res, Div Med Oncol A, I-00144 Rome, Italy
关键词
mTOR; growth inhibition; angiogenesis; cancer therapy; rapamycin-like agents; renal cell carcinoma; TUBEROUS SCLEROSIS COMPLEX; SINGLE-AGENT TEMSIROLIMUS; RENAL-CELL CARCINOMA; RICH AKT-SUBSTRATE; PHASE-II TRIAL; EVERY; WEEKS; MAMMALIAN TARGET; RAPAMYCIN INHIBITOR; KINASE INHIBITOR; DEFOROLIMUS AP23573;
D O I
10.2174/156800910791517172
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mammalian target of rapamycin (mTOR) is a key protein kinase controlling signal transduction from various growth factors and upstream proteins to the level of mRNA translation and ribosome biogenesis, with pivotal regulatory effects on cell cycle progression, cellular proliferation and growth, autophagy and angiogenesis. The mTOR pathway, and its upstream regulators in the PI3K/PTEN/AKT cascade, are altered in a variety of experimental and human malignancies. This has led to the prediction that mTOR inhibitors may be used as anticancer agents. With the recent approval of two mTOR-targeted drugs (temsirolimus and everolimus) for the treatment of renal cell carcinoma and mantle cell lymphoma, this paradigm has been effectively translated into the clinical setting. In this review, we discuss mTOR biology and regulation, the mode of action of mTOR inhibitors as anti-cancer agents, and current clinical evidence supporting the use of rapamycin-like mTOR inhibitors in cancer treatment.
引用
收藏
页码:484 / 495
页数:12
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