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
相关论文
共 39 条
[1]   PROGESTERONE-RECEPTOR REGULATION IN UTERINE CELLS - STIMULATION BY ESTROGEN, CYCLIC ADENOSINE-3',5'-MONOPHOSPHATE, AND INSULIN-LIKE GROWTH FACTOR-I AND SUPPRESSION BY ANTIESTROGENS AND PROTEIN-KINASE INHIBITORS [J].
ARONICA, SM ;
KATZENELLENBOGEN, BS .
ENDOCRINOLOGY, 1991, 128 (04) :2045-2052
[2]   Randomized phase II study of multiple dose levels of CCI-779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced refractory renal cell carcinoma [J].
Atkins, MB ;
Hidalgo, M ;
Stadler, WM ;
Logan, TF ;
Dutcher, JP ;
Hudes, GR ;
Park, Y ;
Lion, SH ;
Marshall, B ;
Boni, JP ;
Dukart, G ;
Sherman, ML .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :909-918
[3]  
BUCKLEY MF, 1993, ONCOGENE, V8, P2127
[4]   Phosphatidylinositol 3-kinase/AKT-mediated activation of estrogen receptor α -: A new model for anti-estrogen resistance [J].
Campbell, RA ;
Bhat-Nakshatri, P ;
Patel, NM ;
Constantinidou, D ;
Ali, S ;
Nakshatri, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :9817-9824
[5]  
Chan S, 2003, BREAST CANCER RES TR, V82, pS82
[6]   Insulin-like growth factor-I inhibits progesterone receptor expression in breast cancer cells via the phosphatidylinositol 3-kinase/akt/mammalian target of rapamycin pathway: Progesterone receptor as a potential indicator of growth factor activity in breast cancer [J].
Cui, XJ ;
Zhang, P ;
Deng, WL ;
Oesterreich, S ;
Lu, YL ;
Mills, GB ;
Lee, AV .
MOLECULAR ENDOCRINOLOGY, 2003, 17 (04) :575-588
[7]   Issues and progress with protein kinase inhibitors for cancer treatment [J].
Dancey, J ;
Sausville, EA .
NATURE REVIEWS DRUG DISCOVERY, 2003, 2 (04) :296-313
[8]  
DEGRAFFENRIED L, 2002, EUR J CANCER, P158
[9]  
DILLING MB, 1994, CANCER RES, V54, P903
[10]   ACTIVITY OF RAPAMYCIN (AY-22,989) AGAINST TRANSPLANTED TUMORS [J].
ENG, CP ;
SEHGAL, SN ;
VEZINA, C .
JOURNAL OF ANTIBIOTICS, 1984, 37 (10) :1231-1237