Polydatin down-regulates the phosphorylation level of Creb and induces apoptosis in human breast cancer cell

被引:41
作者
Chen, Sijia [1 ]
Tao, Jialong [1 ]
Zhong, Fengyun [1 ]
Jiao, Yang [2 ]
Xu, Jiaying [2 ]
Shen, Qiang [3 ]
Wang, Haichao [4 ]
Fan, Saijun [2 ]
Zhang, Yusong [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 2, Dept Oncol, Suzhou, Jiangsu, Peoples R China
[2] Soochow Univ, Coll Med, Sch Radiat Med & Protect, Suzhou, Jiangsu, Peoples R China
[3] Univ Texas MD Anderson Canc Ctr, Dept Clin Canc Prevent, Div Canc Prevent & Populat Sci, Houston, TX 77030 USA
[4] Feinstein Inst Med Res, 350 Community Dr, Manhasset, NY USA
关键词
ACTIVATED PROTEIN-KINASES; RESVERATROL; EXPRESSION; TUMOR; GROWTH; ANTITUMOR;
D O I
10.1371/journal.pone.0176501
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polydatin (PD), a component isolated from Polygonum cuspidatum, has a number of biological functions. However, the antitumor activity of PD has been poorly investigated. In this study, the effect of PD on cell proliferation was evaluated by thiazolyl blue tetrazolium bromide assay. Cell cycle distribution and apoptosis were investigated by flow cytometry. The phosphorylation levels of panel of phosphor-kinases were detected by human phosphokinase arrays. The expression of several proteins associated with cell cycle and apoptosis were analyzed by Western blot analysis. Results showed that PD effectively inhibited the growth of MDA-MB-231 and MCF-7 breast cancer cell lines. Cell cycle analysis demonstrated that PD induced S-phase cell cycle arrest. Human phosphor-kinase arrays showed that the phosphorylation level of cAMP response element-bingding proteins(Creb) was down-regulated, and the results were further confirmed by Western blot analysis. Western blot analysis showed that the expression of protein of cyclin D1 decreased in a time-and dose-dependent manner. Results suggest that PD is a potential therapeutic natural compound.
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页数:13
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