Ellagic Acid Enhances the Efficacy of PI3K Inhibitor GDC-0941 in Breast Cancer Cells

被引:25
作者
Shi, L. [1 ,2 ]
Gao, X. [1 ,3 ]
Li, X. [1 ]
Jiang, N. [1 ]
Luo, F. [4 ]
Gu, C. [3 ]
Chen, M. [2 ]
Cheng, H. [4 ]
Liu, P. [1 ]
机构
[1] Dalian Med Univ, Inst Canc Stem Cell, Dalian 116044, Peoples R China
[2] Dalian Med Univ, Dept Nutr & Food Sci, Dalian 116044, Peoples R China
[3] Dalian Med Univ, Affiliated Hosp 1, Dept Thorac Surg, Dalian 116011, Peoples R China
[4] Dalian Med Univ, Affiliated Hosp 2, Canc Res Inst, Dalian 116027, Peoples R China
基金
中国国家自然科学基金;
关键词
Breast cancer; combination therapy; ellagic acid; GDC-0941; PI3K; targeted therapy; IN-VITRO; KINASE; GROWTH; PATHWAY; CARCINOGENESIS; PUNICALAGIN; COMBINATION; METASTASIS; RECEPTORS; APOPTOSIS;
D O I
10.2174/1566524015666150505161046
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The fact that the phosphatidylinositol 3 kinase (PI3K) signaling pathway is one of the most frequently deregulated signaling networks has triggered intensive efforts in the development of PI3K pathway inhibitors. However, recent clinical trial data have shown only limited activity of PI3K inhibitors at tolerated doses. Thus, there is an urgent need to identify rational combination therapy to improve the efficacy of PI3K-targeted cancer treatment. In this study, we investigated if dietary compound ellagic acid (EA) could improve the therapeutic efficacy of PI3K inhibitor GDC-0941 in breast cancer. Specifically, using a panel of breast cancer cell lines, we showed that combined use of EA and GDC-0941 significantly inhibited cell growth under attached and detached conditions, blocked migration and invasion in vitro as well as tumor initiation and metastasis in vivo. Furthermore, we found that EA promoted apoptosis and further reduced AKT/mTOR activation in GDC-0941-treated breast cancer cells. Together, our data suggest that EA may be a safe and effective agent to boost the efficacy of PI3K-directed breast cancer therapy and that such drug combination may merit further clinical investigation.
引用
收藏
页码:478 / 486
页数:9
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