Anti-tumor effect of hot aqueous extracts from Sonchus oleraceus (L.) L. and Juniperus sabina L - Two traditional medicinal plants in China

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• 作者：Ting Huyan^a ; ¹ ; Qi Li^a ; ¹ ; ^{liqi_1111@nwpu.edu.cn" class="auth_mail" title="E-mail the corresponding author} ; Yi-Lin Wang^a ; Jing Li^a ; Jian-Yang Zhang^a ; Ya-Xiong Liu^a ; Muhammad Riaz Shahid^a ; Hui Yang^a ; Huan-Qing Li^b
• 关键词：Sonchus oleraceus (L.) L. ; Juniperus sabina L ; Inhibition effects ; Apoptosis ; Caspase ; pSTATs
• 刊名：Journal of Ethnopharmacology
• 出版年：2016
• 出版时间：5 June 2016
• 年：2016
• 卷：185
• 期：Complete
• 页码：289-299
• 全文大小：7833 K

文摘

Sonchus oleraceus (L.) L (SO) and Juniperus sabina L (JS) are traditional medicinal plants in China. And the aqueous extracts of them have been used to treat tumor, inflammatory diseases, infection and so on in Chinese folk culture. However, the underlying mechanisms of their anti-tumor activities have not been illustrated yet.

Objective

This study aims to evaluate the inhibitory effects of aqueous extracts from SO and JS on tumor cells.

Materials and methods

The prepared aqueous extracts of SO and JS were used to treat HepG-2 and K562 tumor cells, while the human peripheral blood mononuclear cells (PBMCs) were set as normal control. The viabilities, cell cycle and apoptosis of tumor cells after extracts treatment were assessed, in addition the expression of apoptosis-related genes (FasL, caspase 3, 6, 7, 8, 9, and 10) were analyzed. Meanwhile, the adherence and migration of HepG-2 were tested, and the expression levels of MMPs and ICAM-1 were analyzed. On top of that, the pSTAT in the two cells were also analyzed and suggested the related signaling pathway that the extracts acted on with in these tumor cells.

Results

Results showed that aqueous extracts of SO and JS have inhibitory effects on HepG-2 and K562 cells by decreasing cell viability and inducing apoptosis via up-regulation of the expression of the apoptosis-related genes FasL, caspase 3 and caspase 9. The extracts had different IC₅₀ on tumor cells and PBMCs, which could block the tumor cell cycle at the G⁰/G¹ stage and significantly inhibit the adherence of HepG-2 cells. The extracts inhibited migration of these cells by inhibiting the expression of ICAM-1, MMP-2 and MMP-9. Further study indicated that the inhibition of pSTAT1 and 3 might be responsible for the inhibitory effects of the extracts on tumor cells.

Discussion and conclusion

The results of this study indicated that SO and JS extracts had the anti-tumor effects, which may be developed as novel anti-tumor drugs and used in cancer therapy.