Xue Xiao-Ying, Liu Zhi-He, Jing Feng-Min, Li Yan-Ge, Liu Hui-Zhi, Gao Xian-Shu
Department of Radiation Oncology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei 050000, PR China.
Chin J Cancer. 2010 Oct;29(10):900-6. doi: 10.5732/cjc.010.10141.
The mRNA levels of 59 genes, detected by cDNA microarray, were up-regulated in the radioresistant human esophageal cacinoma cell line TE13R120 as compared with its parental cell line TE13 before and after radiation, and the expression of NRAGE gene showed a gradually up-regulating tendency. This study aimed to further detect the differences of NRAGE gene and protein expression and apoptosis between TE13R120 and TE13 cells, and to investigate the relationship between the NRAGE and the radioresistance of TE13R120 cells and its mechanism.
The two cell lines were irradiated by ⁶⁰Co γ-ray at different conditions. Reverse transcription-polymerase chain reaction (RT-PCR), Western blot, and immunocytochemistry were used to detect the expression of NRAGE. Flow cytometry (FCM) was used to detect the cell apoptosis before and after irradiation.
The mRNA level of NRAGE was higher in TE13R120 cells than in TE13 cells before and after irradiation (before radiation: 0.25 ± 0.03 vs. 0.49 ± 0.03; 4 Gy 4 h: 0.31 ± 0.03 vs. 0.53 ± 0.02; 4 Gy 16 h: 0.32 ± 0.04 vs. 0.59 ± 0.04; 4 Gy 24 h: 0.36 ± 0.05 vs. 0.72 ± 0.04; 2 Gy 12 h: 0.32 ± 0.02 vs. 0.64 ± 0.04; 6 Gy 12 h: 0.36 ± 0.02 vs. 0.79 ± 0.05; 10 Gy 12 h: 0.46 ± 0.04 vs. 0.85 ± 0.01; P < 0.01), and the mRNA level of NRAGE was increased gradually with the increase of radiation dose and time in the two cell lines (P < 0.05 and P < 0.01). Western blot results showed no difference of NRAGE protein level in cytoplasm between TE13R120 cells and TE13 cells before and after irradiation, but its level in nuclei was higher in TE13R120 cells than in TE13 cells at different radiation time and dosages. Immunocytochemistry showed similar results as Western blot. FCM showed no significant difference in apoptosis rate between TE13R120 and TE13 cells before and after radiation.
NRAGE may play an important role in the radiation responses of the two cell lines, and may participate in the formation of radioresistance of TE13R120 cells by changing its subcellular localization, but its relationship with cell apoptosis has not been confirmed.
通过cDNA微阵列检测发现,与亲代细胞系TE13相比,耐辐射人食管癌细胞系TE13R120在辐射前后59个基因的mRNA水平上调,其中NRAGE基因的表达呈逐渐上调趋势。本研究旨在进一步检测TE13R120细胞与TE13细胞中NRAGE基因和蛋白表达及凋亡的差异,探讨NRAGE与TE13R120细胞辐射抗性的关系及其机制。
采用不同条件的⁶⁰Co γ射线照射这两种细胞系。运用逆转录-聚合酶链反应(RT-PCR)、蛋白质免疫印迹法(Western blot)及免疫细胞化学法检测NRAGE的表达。采用流式细胞术(FCM)检测照射前后细胞凋亡情况。
照射前后,TE13R120细胞中NRAGE的mRNA水平均高于TE13细胞(照射前:0.25±0.03 vs. 0.49±0.03;4 Gy 4 h:0.31±0.03 vs. 0.53±0.02;4 Gy 16 h:0.32±0.04 vs. 0.59±0.04;4 Gy 24 h:0.36±0.05 vs. 0.72±0.04;2 Gy 12 h:0.32±0.02 vs. 0.64±0.04;6 Gy 12 h:0.36±0.02 vs. 0.79±0.05;10 Gy 12 h: