Stilbene analogues as inhibitors of breast cancer Stem cells through P-glycoprotein efflux; A 3D quantitative structure-activity relationship study (Inhibitory activity of stilbenes analogues on breast cancer stem cells)

A. Tripathi, K. Misra
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引用次数: 4

Abstract

Some stilbene analogues are essentially important for inhibiting the expression of P-glycoprotein in cancer stem cells. P-glycoprotein is a ATP binding cassette (ABC) transporter that mediates efflux process through ATP hydrolysis. This protein is composed of nucleotide binding and transmembrane domains. The expression level of P-glycoprotein is reported to be high in the cancer stem cell population. Stilbenes are phenylpropanoid-derived naturally occurring secondary metabolites of plants, reported as third generation inhibitors of P-glycoprotein. Based on biological activities of stilbenes against breast cancer cell line, the 3D quantitative structure-activity relationship and docking simulation study was carried out to predict the pharmacophoric features of these compounds. This study is likely to enable researchers to design and synthesize novel therapeutic analogues for reducing the growth of breast cancer stem cells by inhibiting the expression level of P-glycoprotein.
二苯乙烯类似物通过p -糖蛋白外排抑制乳腺癌干细胞二苯乙烯类似物对乳腺癌干细胞抑制活性的三维定量构效关系研究
某些苯乙烯类似物对抑制肿瘤干细胞p -糖蛋白的表达具有重要作用。p -糖蛋白是ATP结合盒(ABC)转运体,通过ATP水解介导外排过程。该蛋白由核苷酸结合和跨膜结构域组成。据报道,p -糖蛋白在肿瘤干细胞群体中的表达水平较高。二苯乙烯是类苯丙烷衍生的植物次生代谢产物,被报道为第三代p糖蛋白抑制剂。根据二苯乙烯类化合物对乳腺癌细胞系的生物活性,进行三维定量构效关系和对接模拟研究,预测化合物的药效特性。这项研究可能使研究人员能够设计和合成新的治疗类似物,通过抑制p -糖蛋白的表达水平来减少乳腺癌干细胞的生长。
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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