Dual blocking of PI3K and mTOR signaling by NVP-BEZ235 inhibits proliferation in cervical carcinoma cells and enhances therapeutic response

被引:33
作者
Xie, Guifang [1 ,2 ,3 ]
Wang, Zhaoyong [4 ]
Chen, Yong [5 ]
Zhang, Shuya [3 ]
Feng, Lu [6 ]
Meng, Fanhui [3 ]
Yu, Zhiyun [1 ,7 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Clin Med, Zhengzhou, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, Zhengzhou, Peoples R China
[3] Jilin Univ, Hosp 1, Dept Obstet & Gynecol, Changchun, Peoples R China
[4] Jilin Univ, Hosp 2, Dept Pathol, Changchun, Peoples R China
[5] Jilin Univ, Hosp 1, Dept Neurosurg, Changchun, Peoples R China
[6] Zhengzhou Univ, Dept Pharm, Affiliated Hosp 1, Zhengzhou, Peoples R China
[7] Zhengzhou Univ, Affiliated Hosp 1, Dept Neurosurg, Zhengzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
NVP-BEZ235; Cervical cancer; Cervical carcinoma; PI3K/mTOR; PHOSPHATIDYLINOSITOL 3-KINASE/MAMMALIAN TARGET; RAPAMYCIN INHIBITOR; GLIOMA-CELLS; IN-VIVO; CANCER; PATHWAY; TEMOZOLOMIDE; AUTOPHAGY; STRATEGY; GROWTH;
D O I
10.1016/j.canlet.2016.11.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
NVP-BEZ235 is a novel dual PI3K/mTOR inhibitor that shows dramatic effects on many tumors, but its effects on cervical carcinoma cells are largely unknown. In the present study, we investigated the effects of NVP-BEZ235 on the proliferation and invasion of cervical carcinoma cells in vitro and clarified its mechanism of action. In cellular settings with human cervical carcinoma cell lines, this molecule effectively and specifically blocked dysfunctional PI3K/mTOR pathway activation, suppressed cell-growth in a time- and concentration-dependent manner, led to G1 cell cycle arrest, and induced apoptosis. NVP-BEZ235 suppressed HeLa cell invasiveness and metastasis by inhibiting the PI3K/Akt/MMP-2 pathway. We further demonstrated that NVP-BEZ235 treatment in combination with cisplatin or carboplatin induced a synergistic anti-tumoral response in cervical carcinoma cells. These findings suggested that NVP-BEZ235 could regulate growth and invasion of cervical carcinoma cells; thus it may provide a potential therapy for cervical carcinoma. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:12 / 20
页数:9
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