Yao Kai, Gao Xiao-yan, Huang Bi-jun, Li Zai-shang, Zhou Fang-jian, Li Ben-yi, Han Hui
Department of Urology, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.
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Zhonghua Yi Xue Za Zhi. 2013 Nov 12;93(42):3360-3.
To explore the roles of different casein kinase 2 (CK2) catalytic subunits in androgen receptor (AR) signaling in prostate cancer cell lines.
Prostate cancer cell lines were maintained.Immunofluorescent staining was performed to determine AR nuclear translocation in PC-3/AR cells with R1881 pretreatment and luciferase gene reporter assay used to determine AR transactivation in LNCaP cells. And reverse transcription-polymerase chain reaction (RT-PCR) was employed to evaluate the mRNA level of prostate-specific antigen (PSA).
R1881-induced AR nuclear localization was reduced significantly (P < 0.01).R1881-stimulated ARE-LUC reporter activity in LNCaP cells decreased with reduced level of PSA mRNA, an AR endogenous target (P < 0.05). To confirm the target specificity, the gene-specific siRNAs were used for both CK2α and CK2α' subunits. The results of ARE-LUC assay (38.5 vs 31.4) suggested that both CK2 catalytic subunits were involved in androgen-stimulated AR nuclear translocation and AR-mediated gene expression in prostate cancer cells.
Both CK2 catalytic subunits are involved in androgen receptor signaling of prostate cancer cells.
探讨不同酪蛋白激酶2(CK2)催化亚基在前列腺癌细胞系雄激素受体(AR)信号传导中的作用。
培养前列腺癌细胞系。采用免疫荧光染色法检测经R1881预处理的PC-3/AR细胞中AR的核转位情况,并用荧光素酶基因报告基因检测法测定LNCaP细胞中AR的反式激活作用。采用逆转录-聚合酶链反应(RT-PCR)评估前列腺特异性抗原(PSA)的mRNA水平。
R1881诱导的AR核定位显著降低(P < 0.01)。R1881刺激的LNCaP细胞中ARE-LUC报告基因活性随AR内源性靶标PSA mRNA水平降低而下降(P < 0.05)。为证实靶标特异性,针对CK2α和CK2α'亚基使用了基因特异性小干扰RNA(siRNA)。ARE-LUC检测结果(38.5对31.4)表明,CK2的两个催化亚基均参与前列腺癌细胞中雄激素刺激的AR核转位和AR介导的基因表达。
CK2的两个催化亚基均参与前列腺癌细胞的雄激素受体信号传导。