Anti-Proliferative Activities of Terpenoids Isolated from Alisma orientalis and their Structure-Activity Relationships

被引:40
作者
Xu, Wen [1 ]
Li, Ting [2 ]
Qiu, Jian-Fang [1 ]
Wu, Shui-Sheng [1 ]
Huang, Ming-Qing [1 ]
Lin, Li-Gen [2 ]
Zhang, Qing-Wen [2 ]
Chen, Xiu-Ping [2 ]
Lu, Jin-Jian [2 ]
机构
[1] Fujian Univ Tradit Chinese Med, Coll Pharm, Fuzhou, Peoples R China
[2] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
基金
中国国家自然科学基金;
关键词
Alisma orientalis; alisol B; anti-proliferative; protostane; structure-activity relationships; triterpenoid; PROTOSTANE-TYPE TRITERPENES; ABSOLUTE STEREOSTRUCTURES; AQUATIC PLANTS; CRUDE DRUGS; B ACETATE; RHIZOMA; APOPTOSIS; CONSTITUENTS; CANCER; CELLS;
D O I
10.2174/1871520614666140601213514
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
This study aimed to isolate terpenoids from Alisma orientalis (Sam.) Juzep. and elucidate their antiproliferative activities, as well as structure-activity relationships. Fourteen protostane-type triterpenoids were isolated from the rhizome of A. orientalis. Among these triterpenoids, alisol A (1), alisol A 24-acetate (2), alisol B (3), alisol B 23-acetate (4), and alisol G (8) presented inhibitory effects on cancer cell lines tested. Compounds 3 and 4 showed the highest potential; IC50 values for HepG2, MDA-MB-231, and MCF-7 cells were 16.28, 14.47, and 6.66 mu M for 3 and 18.01, 15.97, and 13.56 mu M for 4, respectively. Based on these results, we concluded that the degree of C-16 oxidation and the double bond between C-13 and C-17 may be significant in anti-proliferative activities. Further study showed that 3 and 4 effectively induced apoptosis, as confirmed by flow cytometry. Increased intracellular calcium concentration and endoplasmic reticulum stress were detected after treatment with 4 in HepG2 cells. Although compounds 1 and 2 induced minimal apoptosis, they evidently delayed the G2/M phase in HepG2 cells. Further study showed that 1-4 also enhanced LC3II expression, indicating autophagy is occured.
引用
收藏
页码:228 / 235
页数:8
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