Panax notoginseng saponins (PNS) inhibits breast cancer metastasis

被引:90
作者
Wang, Peiwei
Cui, Jingang
Du, Xiaoye
Yang, Qinbo
Jia, Chenglin
Xiong, Minqi
Yu, Xintong
Li, Li
Wang, Wenjian
Chen, Yu [1 ]
Zhang, Teng
机构
[1] Shanghai Univ Tradit Chinese Med, Clin Res Inst Integrat Med, Shanghai 200437, Peoples R China
基金
中国国家自然科学基金;
关键词
Panax notoginseng saponins; 4T1 mammary carcinoma; Metastasis; CARCINOMA CELLS; IN-VITRO; EXPRESSION; MIGRATION; EXTRACT; GROWTH; ROOTS; GENES; LUNG; RATS;
D O I
10.1016/j.jep.2014.04.037
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Panax notoginseng (Burkill) F.H. Chen (Araliaceae) has been extensively used as a therapeutic agent to treat a variety of diseases. Panax notoginseng saponins (PNS) consist of major therapeutically active components of Panax notoginseng. PNS inhibit the growth of a variety of tumor cells in vitro and in vivo. The aim of the study is to investigate the effects and underlying mechanisms of PNS on breast cancer metastasis. Materials and methods: 4T1 cell, a highly metastatic mouse breast carcinoma cell line, was utilized for in vitro and in vivo assays. In vitro assays were first performed to examine the effects of PNS on 4T1 cell viability, migration and invasion, respectively. Real-time PCR analyses were also performed to examine the effects of PNS on the expression of genes associated with tumor metastasis. The effect of PNS on 4T1 tumor cell metastasis was further assessed in spontaneous and experimental metastasis models in vivo. Results: PNS treatment exhibited a dose-dependent effect on impairing 411 cell viability in vitro. However, when examined at a lower dose that did not affect cell viability, the migration and invasion of 4T1 cell was remarkably inhibited in vitro. Meanwhile, PNS treatment led to upregulated expression of genes known to inhibit metastasis and downregulated expression of genes promoting metastasis in cultured 4T1 cells. These results suggested a selective effect of PNS on 4T1 migration and invasion. This hypothesis was further addressed in 4T1 metastasis models in vivo. The results showed that the lung metastasis was significantly inhibited by PNS treatment in both spontaneous and experimental metastasis models. Conclusion: Taken together, our results demonstrated an inhibitory effect of PNS on 4T1 tumor metastasis, warranting further evaluation of PNS as a therapeutic agent for treating breast cancer metastasis. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:663 / 671
页数:9
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