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鞣花酸作为一种有效的抗癌药物:体外、体内、计算机模拟和药物输送研究的综合综述。

Ellagic acid as a potent anticancer drug: A comprehensive review on in vitro, in vivo, in silico, and drug delivery studies.

机构信息

Targeted Drug Delivery Research Center, Institute of Pharmaceutical Technology, Mashhad University of Medical Sciences, Mashhad, Iran.

Department of Medical Biotechnology and Nanotechnology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Biotechnol Appl Biochem. 2022 Dec;69(6):2323-2356. doi: 10.1002/bab.2288. Epub 2021 Dec 15.

Abstract

Ellagic acid as a polyphenol or micronutrient, which can be naturally found in different vegetables and fruits, has gained considerable attention for cancer therapy due to considerable biological activities and different molecular targets. Ellagic acid with low hydrolysis and lipophilic and hydrophobic nature is not able to be absorbed in circulation. So, accumulation inside the intestinal epithelial cells or metabolization to other urolithins leads to the limitation of direct evaluation of EA effects in clinical studies. This review focuses on the studies which supported anticancer activity of pure or fruit-extracted ellagic acid through in vitro, in vivo, in silico, and drug delivery methods. The results demonstrate ellagic acid modulates the expression of various genes incorporated in the cancer-related process of apoptosis and proliferation, inflammation related-gens, and oxidative-related genes. Moreover, the ellagic acid formulation in carriers composed of lipid, silica, chitosan, iron- bovine serum albumin nanoparticles obviously enhanced the stable release and confident delivery with minimum loss. Also, in silico analysis proved that ellagic acid was able to be placed at a position of cocrystal ADP, in the deep cavity of the protein target, and tightly interact with binding pocket residues leading to suppression of substrate availability of protein and its activation inhibition.

摘要

鞣花酸作为一种多酚或微量营养素,可在不同的蔬菜和水果中天然存在,由于具有相当多的生物活性和不同的分子靶点,因此在癌症治疗方面引起了相当大的关注。鞣花酸具有低水解性和亲脂性、疏水性,不能在循环中被吸收。因此,在肠上皮细胞内积累或代谢为其他 urolithins 会限制直接评估 EA 在临床研究中的作用。这篇综述重点介绍了通过体外、体内、计算和药物输送方法支持纯鞣花酸或水果提取鞣花酸抗癌活性的研究。结果表明,鞣花酸调节与细胞凋亡和增殖、炎症相关基因和氧化相关基因相关的各种基因的表达。此外,由脂质、二氧化硅、壳聚糖、铁-牛血清白蛋白纳米粒子组成的载体中的鞣花酸配方明显增强了稳定释放和自信传递,损失最小。此外,计算分析表明,鞣花酸能够位于 cocrystal ADP 的位置,在蛋白质靶标的深腔中,并与结合口袋残基紧密相互作用,从而抑制蛋白质底物的可用性及其激活抑制。

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