Varol Nuray, Konac Ece, Bilen Cenk Y
Department of Medical Biology and Genetics, Faculty of Medicine, Gazi University, Besevler, 06510 Ankara, Turkey.
Department of Medical Biology and Genetics, Faculty of Medicine, Gazi University, Besevler, 06510 Ankara, Turkey
Exp Biol Med (Maywood). 2015 May;240(5):624-30. doi: 10.1177/1535370214556951. Epub 2014 Oct 27.
DNA methylation is considered as one of the most important epigenetic mechanisms and it is catalyzed by DNA methyltransferases (DNMTs). DNMT1 abundance has been frequently seen in urogenital system tumors but the reasons for this abundance are not well understood. We aimed to look into the effects of Wnt/β-catenin signaling pathway on overexpression of DNMT1 and aberrant expression of UHRF1 and HAUSP which are responsible for stability of DNMT1 at transcriptional and protein levels in urogenital cancers. In this context, firstly, Wnt/β-catenin signaling pathway was activated by using SB216763 which is a glycogen synthase kinase-3 (GSK3) β inhibitor. Cell proliferation levels in bladder cancer cells, renal cell carcinoma, and prostate cancer cells treated with GSK3β inhibitor (SB216763) were detected by WST-1 reagent. WIF-1 gene methylation profile was determined by methylation-specific PCR (MSP); expression levels of target genes β-catenin and WIF-1 by real-time PCR; and protein levels of β-catenin, DNMT1, pGSK3β(Ser9), HAUSP, and UHRF1 by Western Blot. Our results indicated that treatment with SB216763 caused an increased cell proliferation at low dose. mRNA levels of β-catenin increased after treatment with SB216273 and protein levels of pGSK3β(Ser9), β-catenin, and DNMT1 increased in comparison to control. HAUSP and UHRF1 were either up-regulated or down-regulated at the same doses depending on the type of cancer. Also, we showed that protein levels of DNMT1, β-catenin, HAUSP, and UHRF1 decreased after re-expression of WIF-1 following treatment with DAC. In Caki-2 cells, β-catenin pathway might have accounted for the stability of DNMT1 expression, whereas such relation is not valid for T24 and PC3 cells. Our findings may offer a new approach for determination of molecular effects of Wnt/β-catenin signal pathway on DNMT1. This may allow us to identify new molecular targets for the treatment of urogenital cancers.
DNA甲基化被认为是最重要的表观遗传机制之一,它由DNA甲基转移酶(DNMTs)催化。DNMT1的丰度在泌尿生殖系统肿瘤中经常可见,但其丰度增加的原因尚不清楚。我们旨在研究Wnt/β-连环蛋白信号通路对DNMT1过表达以及UHRF1和HAUSP异常表达的影响,这两种蛋白在转录和蛋白质水平上对泌尿生殖系统癌症中DNMT1的稳定性起作用。在此背景下,首先,使用糖原合酶激酶-3(GSK3)β抑制剂SB216763激活Wnt/β-连环蛋白信号通路。用WST-1试剂检测用GSK3β抑制剂(SB216763)处理的膀胱癌细胞、肾细胞癌和前列腺癌细胞的细胞增殖水平。通过甲基化特异性PCR(MSP)测定WIF-1基因甲基化谱;通过实时PCR测定靶基因β-连环蛋白和WIF-1的表达水平;通过蛋白质印迹法测定β-连环蛋白、DNMT1、pGSK3β(Ser9)、HAUSP和UHRF1的蛋白质水平。我们的结果表明,低剂量SB216763处理导致细胞增殖增加。与对照组相比,用SB216273处理后β-连环蛋白的mRNA水平增加,pGSK3β(Ser9)、β-连环蛋白和DNMT1的蛋白质水平增加。HAUSP和UHRF1在相同剂量下根据癌症类型上调或下调。此外,我们表明在用DAC处理后重新表达WIF-1后,DNMT1、β-连环蛋白、HAUSP和UHRF1的蛋白质水平降低。在Caki-2细胞中,β-连环蛋白通路可能解释了DNMT1表达的稳定性,而这种关系在T24和PC3细胞中无效。我们的发现可能为确定Wnt/β-连环蛋白信号通路对DNMT1的分子效应提供一种新方法。这可能使我们能够识别治疗泌尿生殖系统癌症的新分子靶点。