Department of Pharmaceutical Oncology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Eur J Cancer. 2010 Mar;46(5):954-65. doi: 10.1016/j.ejca.2009.12.024. Epub 2010 Jan 14.
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.
Y 盒结合蛋白 1(YB-1)通过转录激活耐药基因和生长因子受体基因,在获得全局耐药和促进细胞生长方面发挥关键作用。在这项研究中,我们研究了 YB-1 是否参与调节人类癌细胞的细胞周期和细胞增殖。YB-1 siRNA 的处理导致癌细胞的细胞增殖和细胞周期相关基因 CDC6 的表达明显受到抑制。在癌细胞的细胞周期中,YB-1 的敲低特异性地降低了 S 期含量。CDC6 的过表达消除了对细胞增殖和 S 期进入的这种抑制作用。ChIP 分析表明 YB-1 结合到 CDC6 基因启动子区域的 Y 盒。当用 YB-1 siRNA 处理时,细胞周期蛋白 D1、CDK1 和 CDK2 的表达也减少,同时 p21(Cip1)和 p16(INK4A)的表达增加。此外,乳腺癌患者的核 YB-1 表达与 CDC6 核表达水平显著相关。总之,YB-1 在人类癌细胞的 G1/S 期细胞周期进展中发挥重要作用。因此,YB-1 可能是与 CDC6 密切相关的肿瘤生长和细胞周期的有效生物标志物。