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大罗伞三萜皂苷及其对MDA-MB-231细胞增殖的抑制机制

Triterpenoid Saponins from Ardisia gigantifolia and Mechanism on Inhibiting Proliferation of MDA-MB-231 Cells.

作者信息

Mu Li-Hua, Yan Hong, Wang Yu-Ning, Yu Teng-Fei, Liu Ping

机构信息

Department of Clinical Pharmacology, Chinese PLA General Hospital.

Department of Obstetrics and Gynecology, Chinese PLA General Hospital.

出版信息

Biol Pharm Bull. 2019 Feb 1;42(2):194-200. doi: 10.1248/bpb.b18-00569. Epub 2018 Nov 21.

DOI:10.1248/bpb.b18-00569
PMID:30464092
Abstract

Seventeen 13,28-epoxy triterpenoid saponins obtained from Ardisia gigantifolia STAPF. were evaluated their anti-proliferative activities on MCF-7 cells. The structure-activity relationship analysis indicated that CH group at C-30, four saccharide units with L-rhamnose at R6 in the sugar units are crucial for the cytotoxic activity on MCF-7. Compounds 1, 2, 6, 7, 12, and 14 were selected to identify the anti-proliferative activity on the other three breast cancer cell lines (T47D, MDA-MB-231 and SK-BR-3). Compounds 2, 6, and 7 with good activity on MCF-7 also showed activity on T47D, MDA-MB-231, and SK-BR-3. Compounds 12 and 14 without cytotoxic activity on MCF-7 almost showed no activities on the other three cell lines. For the triple-negative breast cancer MDA-MB-231, Saponins 7 and 14 showed selective cytotoxic activity, 7 showed much more activity than 14, suggesting the six saccharide units in sugar units and CH on C-30 were the key moieties for the anti-proliferative activities. Further molecular mechanism of saponin 7 was studied on inhibiting cell proliferation of MDA-MB-231 cells. Saponin 7 could enhance apoptosis, arrest cell cycles, decrease mitochondrial membrane potentials (MMPs), and considered the involvement of reactive oxygen species (ROS) may explain this conundrum.

摘要

对从大罗伞(Ardisia gigantifolia STAPF.)中获得的17种13,28-环氧三萜皂苷进行了MCF-7细胞抗增殖活性评估。构效关系分析表明,C-30位的CH基团、糖单元中R6位带有L-鼠李糖的四个糖单元对MCF-7细胞的细胞毒性活性至关重要。选择化合物1、2、6、7、12和14对其他三种乳腺癌细胞系(T47D、MDA-MB-231和SK-BR-3)进行抗增殖活性鉴定。在MCF-7细胞上具有良好活性的化合物2、6和7在T47D、MDA-MB-231和SK-BR-3细胞系上也表现出活性。在MCF-7细胞上无细胞毒性活性的化合物12和14在其他三种细胞系上几乎没有活性。对于三阴性乳腺癌MDA-MB-231,皂苷7和14表现出选择性细胞毒性活性,7的活性比14高得多,表明糖单元中的六个糖单元和C-30位的CH是抗增殖活性的关键部分。进一步研究了皂苷7抑制MDA-MB-231细胞增殖的分子机制。皂苷7可增强细胞凋亡、阻滞细胞周期、降低线粒体膜电位(MMPs),并且认为活性氧(ROS)的参与可能解释这一难题。

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