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反向分子对接阐明蛇麻草天然产物黄腐酚及其代谢物的抗癌潜力

Inverse Molecular Docking Elucidating the Anticarcinogenic Potential of the Hop Natural Product Xanthohumol and Its Metabolites.

作者信息

Kores Katarina, Kolenc Zala, Furlan Veronika, Bren Urban

机构信息

Laboratory of Physical Chemistry and Chemical Thermodynamics, Faculty for Chemistry and Chemical Technology, University of Maribor, Smetanova 17, SI-2000 Maribor, Slovenia.

Department of Applied Natural Sciences, Faculty of Mathematics, Natural Sciences and Information Technologies, University of Primorska, Glagoljaška 8, SI-6000 Koper, Slovenia.

出版信息

Foods. 2022 Apr 26;11(9):1253. doi: 10.3390/foods11091253.

Abstract

Natural products from plants exert a promising potential to act as antioxidants, antimicrobials, anti-inflammatory, and anticarcinogenic agents. Xanthohumol, a natural compound from hops, is indeed known for its anticarcinogenic properties. Xanthohumol is converted into three metabolites: isoxanthohumol (non-enzymatically) as well as 8- and 6-prenylnaringenin (enzymatically). An inverse molecular docking approach was applied to xanthohumol and its three metabolites to discern their potential protein targets. The aim of our study was to disclose the potential protein targets of xanthohumol and its metabolites in order to expound on the potential anticarcinogenic mechanisms of xanthohumol based on the found target proteins. The investigated compounds were docked into the predicted binding sites of all human protein structures from the Protein Data Bank, and the best docking poses were examined. Top scoring human protein targets with successfully docked compounds were identified, and their experimental connection with the anticarcinogenic function or cancer was investigated. The obtained results were carefully checked against the existing experimental findings from the scientific literature as well as further validated using retrospective metrics. More than half of the human protein targets of xanthohumol with the highest docking scores have already been connected with the anticarcinogenic function, and four of them (including two important representatives of the matrix metalloproteinase family, MMP-2 and MMP-9) also have a known experimental correlation with xanthohumol. Another important protein target is acyl-protein thioesterase 2, to which xanthohumol, isoxanthohumol, and 6-prenylnaringenin were successfully docked with the lowest docking scores. Moreover, the results for the metabolites show that their most promising protein targets are connected with the anticarcinogenic function as well. We firmly believe that our study can help to elucidate the anticarcinogenic mechanisms of xanthohumol and its metabolites as after consumption, all four compounds can be simultaneously present in the organism.

摘要

植物中的天然产物具有作为抗氧化剂、抗菌剂、抗炎剂和抗癌剂的巨大潜力。来自啤酒花的天然化合物黄腐酚确实以其抗癌特性而闻名。黄腐酚可转化为三种代谢产物:异黄腐酚(非酶促转化)以及8-和6-异戊烯基柚皮素(酶促转化)。采用反向分子对接方法研究黄腐酚及其三种代谢产物,以识别它们潜在的蛋白质靶点。我们研究的目的是揭示黄腐酚及其代谢产物潜在的蛋白质靶点,以便基于所发现的靶蛋白阐述黄腐酚潜在的抗癌机制。将所研究的化合物对接至蛋白质数据库中所有人类蛋白质结构的预测结合位点,并检查最佳对接构象。确定与成功对接化合物得分最高的人类蛋白质靶点,并研究它们与抗癌功能或癌症的实验联系。将所得结果与科学文献中现有的实验结果进行仔细核对,并使用回顾性指标进一步验证。对接得分最高的黄腐酚的人类蛋白质靶点中,超过一半已与抗癌功能相关联,其中四个(包括基质金属蛋白酶家族的两个重要代表,MMP-2和MMP-9)也与黄腐酚存在已知的实验相关性。另一个重要的蛋白质靶点是酰基蛋白硫酯酶2,黄腐酚、异黄腐酚和6-异戊烯基柚皮素以最低的对接得分成功对接至该靶点。此外,代谢产物的研究结果表明,它们最有前景的蛋白质靶点也与抗癌功能相关。我们坚信,我们的研究有助于阐明黄腐酚及其代谢产物的抗癌机制,因为在摄入后,所有这四种化合物可同时存在于生物体内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d573/9104229/cd1bebd2223f/foods-11-01253-g001.jpg

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