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从苦叶树中提取的互变异构植物甾醇及其抗宫颈癌活性。

Tautomeric phytosterols from Vernonia amygdalina Delile and their anti-cervical cancer activity.

机构信息

Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.

Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.

出版信息

Bioorg Chem. 2022 Nov;128:106068. doi: 10.1016/j.bioorg.2022.106068. Epub 2022 Aug 1.

Abstract

Vernonia amygdalina Delile is generally used as green vegetables for cuisine in Nigeria and health tea or products in southeast of china. It was also used as folk medicine for the treatment of anti-helminth, febrifuge, digestive tonic and wounds. In this study, eleven undescribed phytosterols (1-2, 4-12) and six known analogues (3, 13-17) were isolated from the stems of V. amygdalina. Their structures including absolute configurations were elucidated by comprehensive spectroscopic methods (1D and 2D NMR, HRESIMS), X-ray diffraction and comparison of their ECD spectra. Besides, the tautomerism of phytosterols (1, 3-6, 12-17) with hemiacetal moiety were analyzed by solution NMR with different deuterated solvent and variable-temperature experiments. In addition, the cytotoxic activities of isolates against HeLa cells were evaluated. As a result, compound 10 exhibited the most potent anti-cervical cancer activity with the IC of 22.44 μM. Mechanism studies indicated that 10 triggered HeLa cells apoptosis through activating caspase signaling pathway. Furthermore, 10 could arrest the cell cycle in S phase and suppress the activation of the PI3K/AKT/mTOR pathway, leading to the inhibition of HeLa cells proliferation.

摘要

苦枥木树通常在尼日利亚被当作绿色蔬菜食用,在中国东南部则被当作健康茶饮或产品。它也被用作民间药物,用于治疗驱虫、退热、助消化和治疗创伤。在这项研究中,从苦枥木树的茎中分离出了 11 种未被描述的植物甾醇(1-2、4-12)和 6 种已知类似物(3、13-17)。通过综合光谱方法(1D 和 2D NMR、HRESIMS)、X 射线衍射和比较它们的 ECD 光谱,确定了它们的结构,包括绝对构型。此外,通过不同氘代溶剂和变温实验的溶液 NMR 分析了具有半缩醛部分的植物甾醇(1、3-6、12-17)的互变异构现象。此外,还评估了分离物对 HeLa 细胞的细胞毒性。结果表明,化合物 10 对宫颈癌的抑制活性最强,IC 为 22.44 μM。机制研究表明,10 通过激活 caspase 信号通路诱导 HeLa 细胞凋亡。此外,10 可以将细胞周期阻滞在 S 期,并抑制 PI3K/AKT/mTOR 通路的激活,从而抑制 HeLa 细胞的增殖。

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