Flavonoid Compounds of Buah Merah (Pandanus conoideus Lamk) as a Potent Oxidative Stress Modulator in ROS-induced Cancer: In Silico Approach

A. Umar, Faruk Jayanto Kelutur, J. H. Zothantluanga
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引用次数: 8

Abstract

Buah Merah, a typical fruit from Papua, Indonesia which is used empirically in cancer therapy is rich in carotenoids and flavonoids. However, the mechanisms by which Buah Merah ameliorates cancer remained unknown. Natural antioxidant enzymes and pro-oxidant enzymes modulation significantly suppressed ROS production and cancer growth. Therefore, the determination of target enzymes of Buah Merah contents was studied through an in silico approach. Carotenoid and flavonoid compounds from Buah Merah were docked to 7 ROS modulating enzymes using Autodock Vina and the interaction stability was studied using the CABS Flex 2.0 server. The crucial amino acids of each enzyme were determined using DockFlin and prediction of acute oral toxicity of each test ligand was studied using ProTox-II. Based on the molecular docking results, quercetin 3'-glucoside is the most potent compound in binding to CAT, GR, GPx, SOD, LOX, and NOX with binding energy values of -11.2, -9.7, -8.6, -10.2, -10.7, and -12.8 kcal/mol, respectively. Meanwhile, taxifolin 3-O-α-arabinopyranose produced the highest binding affinity of -10.0 kcal/mol at the XO. Each test ligand formed stable interactions with ROS modulating enzymes and formed bonds with crucial amino acids resulting in strong adhesion compared to native and reference ligands. The glucoside group of quercetin 3'-glucoside plays an essential role in determining the proper position in the attachment and supports the formation of hydrogen bonds with receptors. With low acute oral toxicity, it can be concluded that quercetin 3'-glucoside from Buah Merah is a potent oxidative stress modulator in cancer prevention and therapy.
在ROS诱导的癌症中作为有效氧化应激调节剂的Buah Merah(Pandanus conoideus Lamk)黄酮类化合物的Silico方法
Buah Merah是一种典型的来自印度尼西亚巴布亚的水果,在癌症治疗中有着丰富的类胡萝卜素和黄酮类化合物。然而,Buah Merah改善癌症的机制仍然未知。天然抗氧化酶和前氧化酶调节显著抑制ROS的产生和癌症的生长。因此,采用计算机模拟方法研究了Buah Merah含量的目标酶的测定。使用Autodock Vina将Buah Merah的类胡萝卜素和类黄酮化合物与7种ROS调节酶对接,并使用CABS Flex 2.0服务器研究相互作用的稳定性。使用DockFlin测定每种酶的关键氨基酸,并使用ProTox II研究每种测试配体的急性口服毒性预测。根据分子对接结果,槲皮素3'-葡萄糖苷是与CAT、GR、GPx、SOD、LOX和NOX结合最有效的化合物,结合能值分别为-11.2、-9.7、-8.6、-10.2、-10.7和-12.8 kcal/mol。同时,taxifolin 3-O-α-阿拉伯锥糖在XO处产生最高的结合亲和力,为-10.0kcal/mol。与天然配体和参考配体相比,每个测试配体与ROS调节酶形成稳定的相互作用,并与关键氨基酸形成键,从而产生强粘附性。槲皮素3'-葡萄糖苷的葡萄糖苷基团在确定附着物的适当位置方面起着重要作用,并支持与受体形成氢键。由于急性口服毒性低,因此可以得出结论,Buah Merah的槲皮素3’-葡萄糖苷是癌症预防和治疗中有效的氧化应激调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
10
审稿时长
15 weeks
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