mTOR in breast cancer: Differential expression in triple-negative and non-triple-negative tumors

被引:61
|
作者
Walsh, S. [2 ]
Flanagan, L. [1 ]
Quinn, C. [1 ]
Evoy, D. [2 ]
McDermott, E. W. [2 ]
Pierce, A. [2 ]
Duffy, M. J. [1 ,2 ]
机构
[1] St Vincents Univ Hosp, Dept Pathol & Lab Med, Dublin 4, Ireland
[2] Univ Coll Dublin, Conway Inst, UCD Sch Med & Med Sci, Dublin 2, Ireland
来源
BREAST | 2012年 / 21卷 / 02期
基金
爱尔兰科学基金会;
关键词
Breast cancer; Triple-negative; mTOR; Rapamycin; TARGET; PATHWAY; CELLS;
D O I
10.1016/j.breast.2011.09.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer (TNBC) is defined by the absence of estrogen receptors (ER), progesterone receptors (PR) and overexpression of HER2. Targeted therapy is currently unavailable for this subgroup of breast cancer patients. mTOR controls cancer cell growth, survival and invasion and is thus a potential target for the treatment of patients with TNBC. Using immunohistochemistry, mTOR and p-mTOR were measured in 89 TNBCs and 99 non-TNBCs. While mTOR expression was confined to tumor cell cytoplasm, p-mTOR staining was located in the nucleus, perinuclear area and in the cytoplasm. Potentially important, was our finding that nuclear p-mTOR was found more frequently in triple-negative than non triple-negative cancers (p < 0.001). These results suggest that mTOR may play a more important role in the progression of TNBC compared to non-TNBC. Based on these findings, we conclude that mTOR may be a new target for the treatment of triple-negative breast cancer. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:178 / 182
页数:5
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