Timosaponin AIII induces apoptosis and autophagy in human melanoma A375-S2 cells

被引:35
|
作者
Wang, Ye [1 ]
Xu, Lei [1 ]
Lou, Li-Li [1 ,2 ]
Song, Shao-Jiang [2 ]
Yao, Guo-Dong [1 ]
Ge, Meng-Yao [1 ]
Hayashi, Toshihiko [1 ]
Tashiro, Shin-ichi [3 ]
Onodera, Satoshi [4 ]
Ikejima, Takashi [1 ]
机构
[1] Shenyang Pharmaceut Univ, China Japan Res Inst Med Pharmaceut Sci, 103 Wenhua Rd, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Peoples R China
[3] Kyoto Prefectural Univ Med, Kyoto 6020866, Japan
[4] Showa Pharmaceut Univ, Dept Clin & Biomed Sci, Tokyo 1948543, Japan
基金
中国国家自然科学基金;
关键词
Timosaponin AIII; Apoptosis; Autophagy; NO; JNK; ERK; GROWTH-FACTOR; KAPPA-B; DEATH; CARCINOMA; CANCER; ACTIVATION; P38; ERK;
D O I
10.1007/s12272-016-0763-3
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Timosaponin AIII (AIII), a steroidal saponin isolated from Anemarrhena asphodeloides Bge. Our study showed that AIII induced both apoptosis and autophagy, and autophagy inhibited apoptosis in A375S2 cells. Furtherly, this study was carried out to investigate what kind of cytokines plays an important role in this process. The results revealed that AIII induced apoptosis through activating c-Jun N-terminal protein kinase (JNK) or extracellular signal related kinase (ERK) signaling pathway and generating NO. However, JNK or ERK inhibited autophagy, while NO had no effect on autophagy. Therefore, JNK, ERK or NO regulates two programmed death processes in different ways. AIII did not show obvious cytotoxic effect on human peripheral blood mononuclear cells, which indicated that AIII has less side effects on normal cells, and could be considered as a leading compound for developing novel anticancer drug.
引用
收藏
页码:69 / 78
页数:10
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