Suppr超能文献

基于细胞的计算机模拟和体外特性分析研究显示,杆状魔芋突变体植物分离物对 MCF-7 细胞上的 FXR 受体具有抑制作用。

In silico and in vitro Characterizations of Rodent Tuber (Typhonium flagelliforme) Mutant Plant Isolates against FXR Receptor on MCF-7 Cells.

机构信息

Biotechnology Department, Faculty of Engineering, Bina Nusantara University.

Food Biotechnology Research Center, Bina Nusantara University.

出版信息

J Oleo Sci. 2024;73(10):1349-1360. doi: 10.5650/jos.ess24020.

Abstract

Typhonium flagelliforme (T. flagelliforme) is an Indonesian rodent tuber plant traditionally used to treat cancer diseases. Although gamma-ray irradiation has been used to increase the content in the chemical compounds of the T. flagelliforme plants with anticancer activity ten times effective, the specific effect of the isolated compounds from the mutant plants has never been reported yet. The potential cytotoxic agents were characterized via nuclear magnetic resonance spectroscopy, infrared spectroscopy, and mass spectrometry as stigmasterol and 7α-hydroxyl stigmasterol; and their anticancer activity was investigated. The in silico biochemical profile of the two compounds were analyzed by molecular docking and molecular dynamics simulation to confirm its interaction with the agonist binding site of Farsenoid X receptor (FXR). Stigmasterol and 7α-hydroxyl stigmasterol can act as a competitive regulator with a high-affinity for the FXR. The results also showed that stigmasterol and 7α-hydroxyl stigmasterol were the most potential and active fraction of the T. flagelliforme mutant plant against the MCF-7 human breast cancer cell line, with IC value 9.13 µM and 12.97 µM, compared with cisplastin as a control about 13.20 µM. These results demonstrate the potential of stigmasterol and 7α-hydroxyl stigmasterol in T. flagelliforme mutant plants to act towards cancer diseases.

摘要

香鳞毛蕨(T. flagelliforme)是印度尼西亚的一种根茎类植物,传统上被用于治疗癌症疾病。尽管伽马射线辐射已被用于将具有抗癌活性的 T. flagelliforme 植物中的化合物含量增加到原来的 10 倍,但从未报道过突变体植物中分离出的化合物的具体效果。通过核磁共振波谱、红外光谱和质谱学对这些潜在的细胞毒性剂进行了表征,鉴定出它们分别为豆甾醇和 7α-羟基豆甾醇;并对它们的抗癌活性进行了研究。通过分子对接和分子动力学模拟对这两种化合物的计算机生化特性进行了分析,以确认它们与法尼醇 X 受体(FXR)的激动剂结合位点的相互作用。豆甾醇和 7α-羟基豆甾醇可以作为一种高亲和力的竞争性调节剂作用于 FXR。研究结果还表明,豆甾醇和 7α-羟基豆甾醇是 T. flagelliforme 突变植物中最具潜力和活性的部分,对 MCF-7 人乳腺癌细胞系的 IC50 值分别为 9.13 µM 和 12.97 µM,而顺铂作为对照约为 13.20 µM。这些结果表明,香鳞毛蕨突变体植物中的豆甾醇和 7α-羟基豆甾醇具有治疗癌症的潜力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验