Thompson Alvin D, Kakar Sham S
Department of Biochemistry and Molecular Biology, James Graham Brown Cancer Center, University of Louisville, 580 South Preston, Baxter II, 324, Kentucky 40202, USA.
FEBS Lett. 2005 Jun 6;579(14):3195-200. doi: 10.1016/j.febslet.2005.05.008.
The pituitary tumor transforming Gene (PTTG) is an oncogene that is highly expressed in most tumors analyzed to date. Here, we report the effects of insulin and the insulin like growth factor-1 (IGF-1) on the expression of PTTG. Using MCF-7 cells, a human breast cancer cell line, we observed that both insulin and IGF-1 upregulate the expression of PTTG mRNA by approximately 2.5-fold. Induction of PTTG mRNA expression by insulin or IGF-1 was completely blocked by the specific phosphatidylinositol (PI) 3 kinase inhibitor LY294002, but partially blocked by the MAP kinase inhibitor PD98059. Pretreatment of MCF-7 cells with actinomycin D completely blocked the stimulatory effect of insulin. Transfection of MCF-7 cells with a PTTG promoter-luciferase reporter construct revealed the dose-dependent stimulation of PTTG promoter activity by insulin, suggesting that the increase in PTTG expression by insulin is a result of activation of transcription of the PTTG gene. Taken together, our results suggest that insulin and IGF-1 regulate the expression of PTTG in MCF-7 cells primarily through the activation of PI3K/AKT cascade.
垂体肿瘤转化基因(PTTG)是一种癌基因,在迄今为止分析的大多数肿瘤中均高表达。在此,我们报告胰岛素和胰岛素样生长因子-1(IGF-1)对PTTG表达的影响。使用人乳腺癌细胞系MCF-7细胞,我们观察到胰岛素和IGF-1均使PTTG mRNA的表达上调约2.5倍。胰岛素或IGF-1诱导的PTTG mRNA表达被特异性磷脂酰肌醇(PI)3激酶抑制剂LY294002完全阻断,但被丝裂原活化蛋白激酶抑制剂PD98059部分阻断。用放线菌素D预处理MCF-7细胞可完全阻断胰岛素的刺激作用。用PTTG启动子-荧光素酶报告基因构建体转染MCF-7细胞显示胰岛素对PTTG启动子活性有剂量依赖性刺激作用,这表明胰岛素使PTTG表达增加是PTTG基因转录激活的结果。综上所述,我们的结果表明胰岛素和IGF-1主要通过激活PI3K/AKT级联反应来调节MCF-7细胞中PTTG的表达。