Alimirah Fatouma, Panchanathan Ravichandran, Chen Jianming, Zhang Xiang, Ho Shuk-Mei, Choubey Divaker
Edward Hines Jr. VA Hospital, Hines, IL 60141, USA.
Neoplasia. 2007 Dec;9(12):1152-9. doi: 10.1593/neo.07769.
Increased expression of androgen receptor (AR) in prostate cancer (PC) is associated with transition to androgen independence. Because the progression of PC to advanced stages is often associated with the loss of p53 function, we tested whether the p53 could regulate the expression of AR gene. Here we report that p53 negatively regulates the expression of AR in prostate epithelial cells (PrECs). We found that in LNCaP human prostate cancer cells that express the wild-type p53 and AR and in human normal PrECs, the activation of p53 by genotoxic stress or by inhibition of p53 nuclear export downregulated the expression of AR. Furthermore, forced expression of p53 in LNCaP cells decreased the expression of AR. Conversely, knockdown of p53 expression in LNCaP cells increased the AR expression. Consistent with the negative regulation of AR expression by p53, the p53-null HCT116 cells expressed higher levels of AR compared with the isogenic HCT116 cells that express the wildtype p53. Moreover, we noted that in etoposide treated LNCaP cells p53 bound to the promoter region of the AR gene, which contains a potential p53 DNA-binding consensus sequence, in chromatin immunoprecipitation assays. Together, our observations provide support for the idea that the loss of p53 function in prostate cancer cells contributes to increased expression of AR.
前列腺癌(PC)中雄激素受体(AR)表达增加与向雄激素非依赖状态转变相关。由于PC进展至晚期常与p53功能丧失有关,我们检测了p53是否能调节AR基因的表达。在此我们报告p53在前列腺上皮细胞(PrECs)中负向调节AR的表达。我们发现在表达野生型p53和AR的LNCaP人前列腺癌细胞以及人正常PrECs中,基因毒性应激或抑制p53核输出激活p53后会下调AR的表达。此外,在LNCaP细胞中强制表达p53会降低AR的表达。相反,在LNCaP细胞中敲低p53表达会增加AR的表达。与p53对AR表达的负向调节一致,与表达野生型p53的同基因HCT116细胞相比,p53基因缺失的HCT116细胞表达更高水平的AR。此外,我们注意到在依托泊苷处理的LNCaP细胞中,在染色质免疫沉淀试验中p53与AR基因的启动子区域结合,该区域含有一个潜在的p53 DNA结合共有序列。总之,我们的观察结果支持了前列腺癌细胞中p53功能丧失导致AR表达增加这一观点。