Exploring the role of EZH2 (PRC2) as epigenetic target

Imlimaong Aier, Utkarsh Raj
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引用次数: 1

Abstract

Polycomb group (PcG) proteins have been observed to maintain the pattern of histone by methylation of the histone tail responsible for the gene expression in various cellular processes. The PcG protein consists of two multicomplex, Polycomb Repressive Complexes 1 and 2, which includes Enhancer of zeste homolog 2 (EZH2) acting so that the histones silences tumor suppressor genes. Overexpression of EZH2 results in hyper activation observed in various forms of cancer, for instance, prostate and breast cancer. In the past decade, potent inhibitors for EZH2 have been discovered. However, reports of natural compounds for targeting EZH2 is significantly less. The druglikeness and pharmacokinetic properties of several natural compounds were analyzed and the compound with top inhibitory property was studied by molecular docking. A GLIDE score of -8.223 kcal/mol with stable interaction between the protein and ligand was observed for a simulation of 50 ns. This suggests the use of selected compound as an effective inhibitor for EZH2.
探讨EZH2 (PRC2)作为表观遗传靶点的作用
Polycomb group (PcG)蛋白通过在各种细胞过程中负责基因表达的组蛋白尾部甲基化来维持组蛋白的模式。PcG蛋白由两个多复合物组成,多梳抑制复合物1和2,其中包括zeste同源增强子2 (EZH2),其作用是使组蛋白沉默肿瘤抑制基因。EZH2的过表达导致多种癌症的过度激活,例如前列腺癌和乳腺癌。在过去的十年中,已经发现了EZH2的有效抑制剂。然而,针对EZH2的天然化合物的报道却少得多。分析了几种天然化合物的药物相似性和药动学性质,并通过分子对接研究了具有顶级抑制性能的化合物。在50 ns的模拟时间内,该蛋白与配体的相互作用稳定,GLIDE分数为-8.223 kcal/mol。这表明使用选定的化合物作为EZH2的有效抑制剂。
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