Yang Heejung, Kim Hyun Woo, Kim Young Choong, Sung Sang Hyun
College of Pharmacy, Kangwon National University, Chuncheon, Republic of Korea.
College of Pharmacy and Research Institute of Pharmaceutical Science, Seoul National University, Seoul, Republic of Korea.
Pharmacogn Mag. 2017 Jan-Mar;13(49):118-122. doi: 10.4103/0973-1296.196308.
It is well known that the naturally occurring modified triterpenes in plants have a wide diversity of chemical structures and biological functions. The lupane-, oleanane-, and ursane-type triterpenes are the three major members of natural triterpenes with a wide range of biological properties. A systematic approach is necessary to review their structures and biological activities according to the backbones and the different substituents.
Thirty lupane-(L1-7), oleanane-(O1-14), and ursane-type (U1-9) triterpenes with structural diversity were examined to evaluate their cytotoxic activities against two cancer cell lines, human hepatocellular carcinoma (HepG2) and AGS cells.
They were isolated from , , and using a series of column chromatography methods and were treated to evaluate their cytotoxic activities against HepG2 and AGS human gastric adenocarcinoma cell. Further, two triterpenes showing the most potent activities were subjected to the apoptotic screening assay using flow cytometry.
The polar groups, such as an oxo group at C-1, a free hydroxyl at C-2, C-3, or C-23, and a carboxylic moiety at C-28, as well as the type of backbone, explicitly increased the cytotoxic activity on two cancer cells. O5 and U5 showed significantly the potent cytotoxic activity in comparison to other glycosidic triterpenes. In annexin-V/propidium iodide (PI) staining assay, the percentage of late apoptosis (annexin-V+/PI+) 12 and 24 h after treatment with O5 and U5 at 25 μM increased from 14.5% to 93.1% and from 46.4% to 49.1%, respectively, in AGS cells. The cytotoxicity induced by O5 showed a significant difference compared to U5 for 12 and 24 h.
In the study, we can suggest the potent moieties which influence their cytotoxic activities against two cancer cells. The polar groups at C-1, C-2, C-3, C-23, and C-28 and the linkage of sugar moieties influenced the different cytotoxic activities.
Thirty naturally occurring oleanane-, ursane-, and lupane-type triterpenes were isolated from , , and An oxo, a free hydroxyl, a carboxylic moiety, and the types of aglycone influenced the cell cytotoxicityCorosolic acid and α-hederin showed the most potent cytotoxicity via apoptosis.
众所周知,植物中天然存在的修饰三萜类化合物具有广泛多样的化学结构和生物学功能。羽扇豆烷型、齐墩果烷型和乌苏烷型三萜是天然三萜的三大主要成员,具有广泛的生物学特性。有必要采用系统的方法,根据骨架和不同取代基来综述它们的结构和生物活性。
研究30种具有结构多样性的羽扇豆烷型(L1 - 7)、齐墩果烷型(O1 - 14)和乌苏烷型(U1 - 9)三萜对两种癌细胞系,即人肝癌细胞(HepG2)和AGS细胞的细胞毒性活性。
它们分别从[具体植物1]、[具体植物2]和[具体植物3]中通过一系列柱色谱法分离得到,并进行处理以评估其对HepG2和AGS人胃腺癌细胞的细胞毒性活性。此外,对两种活性最强的三萜采用流式细胞术进行凋亡筛选试验。
C - 1位的羰基、C - 2、C - 3或C - 23位的游离羟基、C - 28位的羧基等极性基团以及骨架类型,均显著增强了对两种癌细胞的细胞毒性活性。与其他糖苷型三萜相比,O5和U5表现出显著的强细胞毒性活性。在膜联蛋白 - V/碘化丙啶(PI)染色试验中,在AGS细胞中,用25 μM的O5和U5处理12小时和24小时后,晚期凋亡(膜联蛋白 - V + /PI +)的百分比分别从14.5%增加到93.1%和从46.4%增加到49.1%。O5诱导的细胞毒性在12小时和24小时时与U5相比有显著差异。
在本研究中,我们可以指出影响其对两种癌细胞细胞毒性活性的有效基团。C - 1、C - 2、C - 3、C - 23和C - 28位的极性基团以及糖基的连接方式影响了不同的细胞毒性活性。
从[具体植物1]、[具体植物2]和[具体植物3]中分离出30种天然存在的齐墩果烷型、乌苏烷型和羽扇豆烷型三萜。羰基、游离羟基、羧基和苷元类型影响细胞毒性。熊果酸和α - 常春藤皂苷通过凋亡表现出最强的细胞毒性。