Bandugula Venkata Reddy, N Rajendra Prasad
Department of Biochemistry and Biotechnology, Annamalai University, Annamalainagar, 608 002, Tamilnadu, India.
Tumour Biol. 2013 Feb;34(1):251-9. doi: 10.1007/s13277-012-0545-6. Epub 2012 Oct 12.
Previously, we reported the radiosensitizing potential of the combination of 2-deoxy-D-glucose (2DG) and ferulic acid (FA) in NCI-H460 non-small cell lung carcinoma cells in vitro. The present study aims to explore the relevant mechanism of cell death induced by the combination of 2DG and FA along with irradiation in NCI-H460 cells. Incubation of NCI-H460 cells with the combination of 2DG and FA for 24 h before irradiation upregulated the expression of proapoptotic proteins p53 and Bax. Combination of 2DG and FA also increased the levels of p21 and GADD45A in NCI-H460 cells. DNA repair inhibition is expected to be a possible mechanism for the radiosensitization observed, which is evidenced by the downregulation of radiation-induced ataxia-telangiectasia mutated gene expression upon treatment with 2DG and/or FA. Moreover, Western blotting analysis of NF-κB and caspase-3 revealed the involvement of apoptotic signals in the cytotoxicity exhibited by the combination of 2DG and FA. Cell cycle analysis data also showed the increased percentage of Sub-G(0) phase cells upon treatment with the combination of 2DG and FA before irradiation. Taken together, the results of our study clearly suggested that the cell death induced by the combination of 2DG and FA along with irradiation would involve alteration in expression of p53, p21, NF-κB, Bax, and caspase-3, indicating oxidative mechanism in NCI-H460 cells.
此前,我们报道了2-脱氧-D-葡萄糖(2DG)与阿魏酸(FA)联合使用对NCI-H460非小细胞肺癌细胞的体外放射增敏潜力。本研究旨在探讨2DG与FA联合照射诱导NCI-H460细胞死亡的相关机制。在照射前,将NCI-H460细胞与2DG和FA联合孵育24小时,上调了促凋亡蛋白p53和Bax的表达。2DG与FA联合使用还增加了NCI-H460细胞中p21和GADD45A的水平。DNA修复抑制有望成为观察到的放射增敏的一种可能机制,这在用2DG和/或FA处理后辐射诱导的共济失调毛细血管扩张突变基因表达下调中得到了证实。此外,对NF-κB和caspase-3的蛋白质印迹分析揭示了凋亡信号参与了2DG与FA联合使用所表现出的细胞毒性。细胞周期分析数据还显示,在照射前用2DG与FA联合处理后,亚G(0)期细胞的百分比增加。综上所述,我们的研究结果清楚地表明,2DG与FA联合照射诱导的细胞死亡涉及p53、p21、NF-κB、Bax和caspase-3表达的改变,表明NCI-H460细胞中存在氧化机制。