首页> 外文会议>2016 International Conference on Bioinformatics and Systems Biology >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)
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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)

机译:Stilbene类似物通过P-糖蛋白外排作为乳腺癌干细胞的抑制剂; 3D定量结构-活性关系研究(Stilbenes类似物对乳腺癌干细胞的抑制活性)

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摘要

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.
机译:一些二苯乙烯类似物对于抑制癌症干细胞中P-糖蛋白的表达至关重要。 P-糖蛋白是一种ATP结合盒(ABC)转运蛋白,可通过ATP水解介导外排过程。该蛋白质由核苷酸结合和跨膜结构域组成。据报道在癌症干细胞群体中P-糖蛋白的表达水平很高。 Stilbenes是植物的苯丙烷类天然衍生的次生代谢产物,据报道是P-糖蛋白的第三代抑制剂。基于对苯二酚对乳腺癌细胞系的生物学活性,进行了3​​D定量构效关系和对接模拟研究,以预测这些化合物的药效学特征。这项研究可能使研究人员能够设计和合成新颖的治疗类似物,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。

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