The Anti-Lung Cancer Activities of Steroidal Saponins of P. polyphylla Smith var. chinensis (Franch.) Hara through Enhanced Immunostimulation in Experimental Lewis Tumor-Bearing C57BL/6 Mice and Induction of Apoptosis in the A549 Cell Line

被引:48
作者
Li, Yu [1 ,2 ,3 ]
Gu, Jun-Fei [2 ]
Zou, Xi [1 ]
Wu, Jian [1 ]
Zhang, Ming-Hua [2 ]
Jiang, Jun [2 ]
Qin, Dong [2 ]
Zhou, Jin-Yong [1 ]
Liu, Bao-Xin-Zi [1 ]
Zhu, Yun-Tao [4 ]
Jia, Xiao-Bin [2 ]
Feng, Liang [2 ]
Wang, Rui-Ping [1 ]
机构
[1] Nanjing Univ Chinese Med, Affiliated Hosp, Dept Oncol, Nanjing 210029, Jiangsu, Peoples R China
[2] Jiangsu Prov Acad Chinese Med, Key Lab New Drug Delivery Syst Chinese Meteria Me, Nanjing 210028, Jiangsu, Peoples R China
[3] Guangxi Univ Chinese Med, Affiliated Hosp 1, Dept Oncol, Nanning 530001, Guangxi, Peoples R China
[4] Nanjing Univ Chinese Med, Clin Med Coll 1, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
P. polyphylla Smith var. chinensis (Franch.) Hara; steroidal saponins; immunostimulation; inflammation; apoptosis; INDUCED OXIDATIVE DAMAGE; LUNG-CANCER; PARIS-POLYPHYLLA; IN-VITRO; MESENCHYMAL TRANSITION; ANTICANCER ACTIVITY; CARCINOMA; CYTOKINES; GROWTH; INFLAMMATION;
D O I
10.3390/molecules181012916
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P. polyphylla Smith var. chinensis (Franch.) Hara (PPSCFH) has been used as medicinal Paris for the prevention and treatment of cancers in China for thousands of years. Its main components, steroidal saponins (PRS), have been confirmed to inhibit tumor growth. In the present study, the immunostimulation of PRS was investigated in Lewis bearing-C57BL/6 mice while the induction of apoptosis in A549 cells was also studied. The treatment with PRS (2.5, 5.0 and 7.5 mg/kg) significantly inhibited tumor, volume, and weight in the C57BL/6 mice. The rates of inhibition of PRS (at 2.5, 5.0 and 7.5 mg/kg) were 26.49 +/- 17.30%, 40.32 +/- 18.91% and 54.94 +/- 16.48%, respectively. The spleen and thymus indexes were increased remarkably, while the levels of inflammatory cytokines including TNF-alpha, IL-8 and IL-10 in serum were decreased according to ELISA assays. For A549 cells, Hoechst 33342 staining and annexin V/PI by flow cytometry showed that PRS (0.25, 0.50 and 0.75 mg/mL) induced nuclear changes of A549 cells with DNA condensation and fragmentations of chromatin, as well as inducing apoptosis. Furthermore, PRS could also attenuate the over-generation of intracellular ROS. Western blotting analysis showed a significant decrease on the expressions of proinflammatory cytokines MCP-1, IL-6 and TGF-beta 1, as well as cell adhesion molecule ICAM-1, by treatment with PRS. Our results demonstrated that the inhibition of PRS on tumor growth might be associated with the amelioration of inflammation responses, induction of apoptosis, as well as the decrease of ROS. These results suggested that PRS implied a potential therapeutic effect in the lung cancer treatment.
引用
收藏
页码:12916 / 12936
页数:21
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