首页> 外文期刊>Journal of Agricultural and Food Chemistry >Theaflavins Depolymerize Microtubule Network through Tubulin Binding and Cause Apoptosis of Cervical Carcinoma HeLa Cells
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Theaflavins Depolymerize Microtubule Network through Tubulin Binding and Cause Apoptosis of Cervical Carcinoma HeLa Cells

机译:茶黄素通过微管蛋白结合解聚微管网络,并导致宫颈癌HeLa细胞凋亡。

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Here we studied the antiproliferative activity of theaflavins in cervical carcinoma HeLa cells by investigating their effects on cellular microtubules and purified goat brain tubulin. Theaflavins inhibited proliferation of HeLa cells with IC_(50) value of 110 ± 2.1 μg/mL (p - < 0.01), caused cell cycle arrest at G2/M phase and induced apoptosis with alteration of expression of pro- and antiapoptotic proteins. Along with these antiproliferative activities, theaflavins act as microtubule depolymerizers. Theaflavins disrupted the microtubule network accompanied by alteration of cellular morphology and also decreased the polymeric tubulin mass of the cells. The polymerization of cold treated depolymerized microtubules in HeLa cells was prevented in the presence of theaflavins, In vitro polymerization of purified tubulin into microtubules was also inhibited by theaflavins with an IC_(50) value of 78 ± 2.43 μg/mL (P < 0.01). Thus, disruption of cellular microtubule network of HeLa cells through microtubule depolymerization may be one of the possible mechanisms of antiproliferative activity of theaflavins.
机译:在这里,我们通过研究茶黄素对宫颈癌HeLa细胞的抑制作用,研究了茶黄素对细胞微管和纯化的山羊脑微管蛋白的作用。茶黄素以110±2.1μg/ mL(p-<0.01)的IC_(50)值抑制HeLa细胞的增殖,引起细胞周期停滞在G2 / M期,并诱导凋亡和促凋亡蛋白和抗凋亡蛋白表达的改变。除这些抗增殖活性外,茶黄素还起微管解聚剂的作用。茶黄素破坏了微管网络,伴随着细胞形态的改变,还降低了细胞的聚合微管蛋白质量。在茶黄素存在下阻止了冷处理的解聚的微管在HeLa细胞中的聚合,茶黄素还抑制了纯化的微管蛋白在体外的聚合成微管,IC_(50)值为78±2.43μg/ mL(P <0.01) 。因此,通过微管解聚破坏HeLa细胞的细胞微管网络可能是茶黄素抗增殖活性的可能机制之一。

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