New targets for therapy in breast cancer - Mammalian target of rapamycin (mTOR) antagonists

被引:83
|
作者
Carraway, H [1 ]
Hidalgo, M [1 ]
机构
[1] Johns Hopkins Univ Hosp, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21287 USA
关键词
CCI-779; epidermal growth factor receptor; mammalian target of rapamycin; phosphatidylinositol 3-kinase pathway; PTEN;
D O I
10.1186/bcr927
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 kinase member of the cellular phosphatidylinositol 3-kinase (PI3K) pathway, which is involved in multiple biologic functions such as transcriptional and translational control. mTOR is a downstream mediator in the PI3K/Akt signaling pathway and plays a critical role in cell survival. In breast cancer this pathway can be activated by membrane receptors, including the HER (or ErbB) family of growth factor receptors, the insulin-like growth factor receptor, and the estrogen receptor. There is evidence suggesting that Akt promotes breast cancer cell survival and resistance to chemotherapy, trastuzumab, and tamoxifen. Rapamycin is a specific mTOR antagonist that targets this pathway and blocks the downstream signaling elements, resulting in cell cycle arrest in the G(1) phase. Targeting the Akt/PI3K pathway with mTOR antagonists may increase the therapeutic efficacy of breast cancer therapy.
引用
收藏
页码:219 / 224
页数:6
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