Lai Paul B S, Chi Tian-Yi, Chen George G
Department of Surgery, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong SAR, China.
Apoptosis. 2007 Feb;12(2):387-93. doi: 10.1007/s10495-006-0571-1.
Induction of p53 gene expression in cancer cells can lead to both cell cycle arrest and apoptosis. To clarify whether the level of p53 expression determines the apoptotic response of hepatocellular carcinoma (HCC) cells, we assessed the effect of various levels of expression of p53 gene on a p53-deficient HCC cell line, Hep3B, utilizing a doxycycline (Dox)-regulated inducible p53 expression system. Our results showed that apoptosis was induced in HCC cells with high levels of p53 expression. However, lower level of p53 expression induced only cell cycle arrest but not apoptosis. Bax expression was up-regulated following high levels of p53 expression, while bcl-2 expression was not altered by the level of p53 expression. Moreover, p21 expression was observed in both high and low expression of p53. These results suggest the level of p53 expression could determine if the HCC cells would go into cell cycle arrest or apoptosis. Bax may participate, at least in part, in inducing p53-dependent apoptosis and the induction of p21 alone was able to cause cell cycle arrest but not apoptosis.
癌细胞中p53基因表达的诱导可导致细胞周期停滞和细胞凋亡。为了阐明p53表达水平是否决定肝细胞癌(HCC)细胞的凋亡反应,我们利用强力霉素(Dox)调控的诱导型p53表达系统,评估了不同水平的p53基因表达对p53缺陷的HCC细胞系Hep3B的影响。我们的结果表明,p53高表达的HCC细胞中诱导了细胞凋亡。然而,较低水平的p53表达仅诱导细胞周期停滞,而不诱导细胞凋亡。p53高表达后Bax表达上调,而bcl-2表达不受p53表达水平的影响。此外,在p53高表达和低表达时均观察到p21表达。这些结果表明,p53表达水平可以决定HCC细胞是进入细胞周期停滞还是发生细胞凋亡。Bax可能至少部分参与诱导p53依赖性细胞凋亡,单独诱导p21能够导致细胞周期停滞,但不能诱导细胞凋亡。