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Chemical Components Analyzed by UPLC-QTOF-MS and In Vitro Antitumor Effects of the Chestnut Mushroom Pholiota adiposa (Agaricomycetes)

文献类型： 外文期刊

作者： Wang, Xiaoyan 1 ; Liu, Yan 2 ; Kong, Fanli 3 ; Li, Gang 3 ;

作者机构： 1.Jilin Agr Sci & Technol Univ, Acad Tradit Chinese Med, Jilin 132109, Peoples R China

2.Changchun Scitech Univ, Acad Med, Changchun 130600, Peoples R China

3.Jilin Acad Agr Sci, Inst Agr Qual Stand & Testing Technol, Changchun 130033, Peoples R China

关键词： Pholiota adiposa; UPLC-QTOF-MS; CCK-8 method; apoptosis; medicinal mushrooms

期刊名称：INTERNATIONAL JOURNAL OF MEDICINAL MUSHROOMS （ 影响因子：1.2； 五年影响因子：1.4 ）

ISSN： 1521-9437

年卷期： 2023 年 25 卷 4 期

页码：

收录情况： SCI

摘要： We investigated the chemical constituents and anti-tumor activity of cultivated Pholiota adiposa in vi-tro using ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry. HepG-2, A549, HeLa, and MCF-7 cells, which are 4 kinds of human cancer cell lines, were cultured in vitro, treated with different concentrations of the ethanol extract of Ph. adiposa (EPA), and cytotoxicity was determined using the cell counting kit-8 assay. Flow cytometry was used to analyze the apoptosis of HepG-2 cells via annexin V-fluorescein isothiocyanate/ propidium iodide double staining. Expression levels of apoptosis-associated proteins were determined via Western blot-ting analysis. Thirty-five components were consistent with those recorded in the chemical composition database, with sterols, fatty acids, and polysaccharide compounds accounting for a relatively high proportion. EPA showed the strongest cytotoxicity against HepG-2 cells, increasing the apoptosis rate up to 23.71 +/- 1.59% at a concentration of 50 mu g/mL. Ph. adiposa has various functional chemical constituents and potential anti-tumor applications. We found that the functional constituents exerted anti-tumor activity by inducing apoptosis. Furthermore, the expression levels of BCL-2-associated X were increased, whereas those of BCL-2 were decreased in cells after treatment with EPA. These results suggest that EPA induces HepG-2 cell apoptosis via a caspase-mediated pathway.

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