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Y-box binding protein-1 (YB-1) promotes cell cycle progression through CDC6-dependent pathway in human cancer cells.

机译:Y盒结合蛋白1(YB 1)促进人类癌细胞中CDC6依赖性途径的细胞周期进程。

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摘要

Y-box binding protein-1 (YB-1) plays pivotal roles in acquisition of global drug resistance and cell growth promotion through transcriptional activation of genes for both drug resistance and growth factor receptors. In this study, we investigated whether YB-1 is involved in regulation of the cell cycle and cell proliferation of human cancer cells. Treatment with YB-1 siRNA caused a marked suppression of cell proliferation and expression of a cell cycle related gene, CDC6 by cancer cells. Of cell cycle of cancer cells, S phase content was specifically reduced by knockdown of YB-1. The overexpression of CDC6 abrogated this inhibition of both cell proliferation and S phase entry. ChIP assay demonstrated that YB-1 binds to a Y-box located in the promoter region of the CDC6 gene. Expression of cyclin D1, CDK1 and CDK2 was also reduced with increased expression of p21(Cip1) and p16(INK4A) when treated with YB-1 siRNA. Furthermore, the nuclear YB-1 expression was significantly associated with the level of CDC6 nuclear expression in patients with breast cancer. In conclusion, YB-1 plays an important role in cell cycle progression at G1/S of human cancer cells. YB-1 thus could be a potent biomarker for tumour growth and cell cycle in its close association with CDC6.
机译:Y-box结合蛋白1(YB-1)在获得全球耐药性和通过耐药性和生长因子受体基因的转录激活促进细胞生长中起关键作用。在这项研究中,我们调查了YB-1是否参与人类癌细胞的细胞周期调控和细胞增殖。用YB-1 siRNA进行治疗可显着抑制癌细胞的增殖和细胞周期相关基因CDC6的表达。在癌细胞的细胞周期中,通过敲除YB-1可以特异性降低S相含量。 CDC6的过表达消除了对细胞增殖和S期进入的抑制。 ChIP分析表明,YB-1与位于CDC6基因启动子区域的Y-box结合。当用YB-1 siRNA处理时,随着p21(Cip1)和p16(INK4A)表达的增加,细胞周期蛋白D1,CDK1和CDK2的表达也降低了。此外,在乳腺癌患者中,核YB-1表达与CDC6核表达水平显着相关。总之,YB-1在人类癌细胞G1 / S的细胞周期进程中起着重要作用。因此,YB-1与CDC6密切相关,可能是肿瘤生长和细胞周期的有效生物标志物。

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