Li Xue-Qin, Pei Dong-Sheng, Qian Guo-Wei, Yin Xiao-Xing, Cheng Qian, Li Lian-Tao, Li Hui-Zhong, Zheng Jun-Nian
Jiangsu Key Laboratory of Biological Cancer Therapy, Xuzhou Medical College, 84 West Huai-hai Road, Xuzhou, 221002, Jiangsu, People's Republic of China.
Tumour Biol. 2011 Oct;32(5):863-72. doi: 10.1007/s13277-011-0187-0. Epub 2011 May 20.
To investigate the effect of methylated oligonucleotide (MON) targeting Ki-67 promoter on the expression of Ki-67 gene and the proliferation and apoptosis of the human 786-0 renal carcinoma cells, human 786-0 cells were transfected with MON. The activity of Ki-67 promoter was detected by dual-luciferase reporter assay system. Among the five methylated oligonucleotides (MON(1)-MON(5)), MON(4) is the best excellent one in the inhibition of the Ki-67 promoter activity. The activity of Ki-67 promoter is decreased to 77.88% in 40-nM group, 50.07% in 80-nM group, 35.63% in 120-nM group, 26.09% in 160-nM group, and 16.98% in 200-nM group compared with 0-nM group. The activity of Ki-67 promoter in MON group is decreased to 61.96% at 8 h, 48.93% at 12 h, 15.97% at 24 h, 26.00% at 36 h, 35.01% at 48 h, 46.08% at 72 h, and 66.12% at 96 h compared with pGLBK235 group. These results show that the effect of MON is time- and dose-dependent. The activity of Ki-67 in MON group is decreased to 16.73% compared with pGLBK235 group, while the control groups have no significant difference. The expression of Ki-67 gene in 786-0 cells was detected by RT-PCR and immunohistochemistry, respectively. The expression of Ki-67 mRNA is decreased to 61.04% and that of Ki-67 protein is decreased to 32.07% in MON group compared with the blank group. The proliferation of 786-0 cells was determined by WST-8. The cell proliferation in MON group is decreased to 61.02% at 24 h, 73.78% at 48 h, 79.72% at 72 h, and 91.53% at 96 h compared with the blank group. The cell apoptosis was measured by annexin V and propidium iodide. The number of apoptosis cells in MON group is 2.42 times of that in the blank group at earlier period and 2.57 times at mid-anaphase. We detected the effect of MON on the expression of bax and p53 by Western blot. Compared with the blank group, the expression of bax protein in MON group is increased by 66.12%, while the expression of p53 is decreased to 67.31%. Our study demonstrates that the methylated oligonucleotide targeting Ki-67 promoter has a remarkable effect on the inhibition of Ki-67 expression and the proliferation of the human 786-0 renal carcinoma cells and can induce apoptosis of the 786-0 cells.
为研究靶向Ki-67启动子的甲基化寡核苷酸(MON)对人786-0肾癌细胞中Ki-67基因表达、细胞增殖及凋亡的影响,将MON转染人786-0细胞。采用双荧光素酶报告基因检测系统检测Ki-67启动子活性。在5种甲基化寡核苷酸(MON(1)-MON(5))中,MON(4)对Ki-67启动子活性的抑制作用最佳。与0 nM组相比,40 nM组Ki-67启动子活性降至77.88%,80 nM组降至50.07%,120 nM组降至35.63%,160 nM组降至26.09%,200 nM组降至16.98%。与pGLBK235组相比,MON组Ki-67启动子活性在8 h时降至61.96%,12 h时降至48.93%,24 h时降至15.97%,36 h时降至26.00%,48 h时降至35.01%,72 h时降至46.08%,96 h时降至66.12%。这些结果表明MON的作用具有时间和剂量依赖性。与pGLBK235组相比,MON组Ki-67活性降至16.73%,而对照组无显著差异。分别采用RT-PCR和免疫组化法检测786-0细胞中Ki-67基因的表达。与空白组相比,MON组Ki-67 mRNA表达降至61.04%,Ki-67蛋白表达降至32.07%。采用WST-8法检测786-0细胞的增殖情况。与空白组相比,MON组细胞增殖在24 h时降至61.02%,48 h时降至73.78%,72 h时降至79.72%,96 h时降至91.53%。采用膜联蛋白V和碘化丙啶检测细胞凋亡情况。早期MON组凋亡细胞数是空白组的2.42倍,中后期是2.57倍。采用Western blot法检测MON对bax和p53表达的影响。与空白组相比,MON组bax蛋白表达增加66.12%,而p53表达降至67.31%。我们的研究表明,靶向Ki-67启动子的甲基化寡核苷酸对抑制人786-0肾癌细胞中Ki-67表达和细胞增殖具有显著作用,并能诱导786-0细胞凋亡。