摘要
目的构建shRNA-Survivin慢病毒载体,对肺腺癌A549细胞中Survivin基因表达进行干扰,探讨其对肿瘤细胞增殖、迁移和凋亡的影响。方法将A549细胞分成3组,即空白对照组,空白病毒载体对照组和shRNA干扰Survivin慢病毒载体组。采用慢病毒载体构建的方法,采用RT-qPCR和Western-Blot检测凋亡因子Caspase-3和Caspase-9的表达量,采用CCK-8试剂盒检测肺癌细胞的增殖,Transwell小室检测肺癌细胞的迁移,AV-PI凋亡试剂盒检测肺癌细胞的凋亡。结果 (1)慢病毒转染效率较高,以肺癌细胞A549为靶点种子细胞,慢病毒转染率为90%;(2)空白载体病毒组的Caspase-3的mRNA的相对表达量(与空白对照组相比)为(1. 231±0. 112,n=3),shRNA-Survivin组的Caspase-3的mRNA的相对表达量为(0.121±0. 009,n=3);两组比较具有统计学差异(t=2. 097,P=0. 0219 <0. 05),Caspase-9的mRNA表达具有相同的趋势;(3) Caspase-3的蛋白相对表达量为(0. 173±0. 231,n=3),shRNA-Survivin组与空白载体病毒组相比,具有统计学差异(t=3.221,P=0.0241<0.05);(4)Transwell实验结果,CCK-8检测结果和AV-PI检测结果显示,空白对照组、空白载体病毒组、shRNA-Survivin组三组之间比较具有明显的统计学差异(P<0.05)。结论 shRNA干扰Survivin可以有效的抑制肺癌细胞的迁移和增殖,并且提高其凋亡率。
Objective The study on the molecular mechanism of shRNA-survivin gene on proliferation,migration and apoptosis of lung cancer cells provides a new way for the treatment of lung cancer cells.Methods Construction building,this research adopts the lentivirus vectors shRNA-Survivin slow virus vector,RT-PCR,Western Blot were used to detect the apoptosis factor Caspase-3 and the expression of Caspase-9,CCK 8 kit to detect lung cancer cell proliferation,Transwell Chambers detection of lung cancer cell migration,AV-PI kit apoptosis detection of lung cancer cell apoptosis.Results (1)Lentiviral transfection efficiency was high.The target cells were lung cancer cell A549,and the transfection rate was 90%.This indicates that lentivirus transfected cells have high transfection efficiency.(2)The relative expression of Caspase-3 mRNA in the blank vector virus group(compared with the blank control group)was(1.231+0.112,n=3);the relative expression of Caspase-3 mRNA in the shRNA-Survivin group(0.121+0.009,n=3);and the difference between the two groups was statistically significant(t=2.097,P=0.0219<0.05).These results indicated that the expression of Caspase-3 in the virus group of shRNA interfering Survivin vectors was lower than that in the virus group of blank vectors.The mRNA of Caspase-9 has the same trend.(3)The relative expression of Caspase-3 protein was(0.173.231,n=3);there was significant difference between shRNA-Survivin group and blank vector virus group(t=3.221,P=0.0241<0.05).These results indicated that the expression of Caspase-3 in the virus group of shRNA interfering Survivin vectors was lower than that in the virus group of blank vectors.(4)Transwell test results,CCK-8 test results and AV-PI test results showed that there were significant statistical differences among the blank control group,blank vector virus group and shRNA-Survivin group(P<0.05).Conclusion shRNA Survivin can effectively inhibit the migration and proliferation of lung cancer cells and increase its apoptosis rate.
作者
吴呈霖
王梅芳
雷怀定
Wu Chenglin;Wang Meifang;Lei Huaiding(Department of Respiratory and critical Care Medicine,Taihe Hospital,Shiyan City(affiliated Hospital of Hubei Medical College),Shiyan 442000,China)
出处
《中华肺部疾病杂志(电子版)》
CAS
2018年第6期683-688,共6页
Chinese Journal of Lung Diseases(Electronic Edition)
基金
湖北省教育厅科学研究计划资助项目:D20152104