Department of Life Science, Division of Molecular and Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Cancer Lett. 2010 Jun 1;292(1):125-32. doi: 10.1016/j.canlet.2009.11.015. Epub 2009 Dec 24.
We investigated the effect of HMGB2 on the stability of p53 protein in HeLa cells. Overexpression of HMGB2 led to accumulation of the p53 protein, whereas HMGB2 knockdown with siRNA resulted in a substantial decrease in the p53 protein level. The HMGB2-dependent increase of p53 stability was specific for HPV-positive HeLa cells as HCT116 and MCF7 cell lines did not demonstrate this response. Co-expression of HMGB2 and HPV E6 prevented HPV E6 protein-mediated ubiquitination and degradation of p53. FACS analysis exhibited that HeLa cells transfected with HMGB2 displayed decreased cell proliferation, with a concomitant increase of the p53 protein and arrest of the cell cycle, predominantly in G1 phase. Our findings collectively suggest that HMGB2 could stabilize p53 by interfering with E6/E6AP-mediated p53 degradation in HPV-positive HeLa cells.
我们研究了 HMGB2 对 HeLa 细胞中 p53 蛋白稳定性的影响。HMGB2 的过表达导致 p53 蛋白积累,而用 siRNA 敲低 HMGB2 则导致 p53 蛋白水平显著下降。HMGB2 依赖性 p53 稳定性增加是 HPV 阳性 HeLa 细胞特有的,因为 HCT116 和 MCF7 细胞系没有表现出这种反应。HMGB2 与 HPV E6 的共表达可防止 HPV E6 蛋白介导的 p53 泛素化和降解。FACS 分析显示,转染 HMGB2 的 HeLa 细胞显示出细胞增殖减少,同时 p53 蛋白增加,细胞周期停滞主要在 G1 期。我们的研究结果表明,HMGB2 可以通过干扰 HPV 阳性 HeLa 细胞中 E6/E6AP 介导的 p53 降解来稳定 p53。