Cytotoxic Steroidal Saponins Containing a Rare Fructosyl from the Rhizomes of Paris polyphylla var. latifolia

植物化学 根茎 赫拉 化学 细胞凋亡 细胞毒性T细胞 皂甙 细胞毒性 糖苷 PI3K/AKT/mTOR通路 天然产物 立体化学 细胞培养 部分 流式细胞术 传统医学 IC50型 生物化学 生物 体外 分子生物学 病理 医学 替代医学 遗传学
作者
Tianyi Li,Yang Du,Minchang Wang,Ke Liu,Yang Liu,Yu Cao,Yuan‐Yuan Wang,Wenwen Chen,Xiao-Ying Qian,Pengcheng Qiu,Hai‐Feng Tang,Yang Lu
出处
期刊:International Journal of Molecular Sciences [Multidisciplinary Digital Publishing Institute]
卷期号:24 (8): 7149-7149 被引量:1
标识
DOI:10.3390/ijms24087149
摘要

A phytochemical investigation of the steroidal saponins from the rhizomes of Paris polyohylla var. latifolia led to the discovery and characterization of three new spirostanol saponins, papolatiosides A–C (1–3), and nine known compounds (4–12). Their structures were established via extensive spectroscopic data analysis and chemical methods. Interestingly, compounds 1 and 2 possessed a fructosyl in their oligosaccharide moiety, which is rare in natural product and was firstly reported in family Melanthiaceae. The cytotoxicity of these saponins against several human cancer cell lines was evaluated by a CCK-8 experiment. As a result, compound 1 exhibited a significant cytotoxic effect on LN229, U251, Capan-2, HeLa, and HepG2 cancer cells with IC50 values of 4.18 ± 0.31, 3.85 ± 0.44, 3.26 ± 0.34, 3.30 ± 0.38 and 4.32 ± 0.51 μM, respectively. In addition, the result of flow cytometry analysis indicated that compound 1 could induce apoptosis of glioma cells LN229. The underlying mechanism was explored by network pharmacology and western bolt experiments, which indicated that compound 1 could induce glioma cells LN229 apoptosis by regulating the EGFR/PI3K/Akt/mTOR pathway.

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