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Effect of cyclin G2 on proliferative ability of SGC-7901 cell

机译:细胞周期蛋白G2对SGC-7901细胞增殖能力的影响

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摘要

AIM: To study the effect of cyclin G2 on proliferation of gastric adenocarcinoma cell line-SGC-7901 cell in vitro.METHODS: By use of cation lipofectamine transfection reagent, the pIRES-G2 and pIRESneo plasmids were transferred into SGC-7901cell line. Anticlones were selected by G418. Positive clones were observed and counted using Giemsa staining. Cell proliferative ability was assayed by MTT.RESULTS: (1) The clone number of pIRES-G2 group decreased, clone volume reduced. The number of cell clones in pIRESneo group was 87 ± 3, that of pIRES-G2 group was 53 ± 4, occupying 60.1% of pIRESneo group, there was significant difference obviously (P < 0.01, t = 15.45). (2) The average absorbance of clone cell obtained by stable transfection of pIRES-G2 at 570 nm was 1.6966 ± 0.2125, the average absorbance of clone cell obtained by stable transfection of pIRESneo at 570 nm was 2.1182 ± 0.3675, there was significant difference between them (P < 0.01, t = 3.412).CONCLUSION: Cyclin G2 can inhibit SGC-7901cell proliferative ability obviously, it may be a negative regulator in cell cycle regulation.
机译:目的:研究细胞周期蛋白G2在体外对胃腺癌细胞SGC-7901细胞增殖的影响。方法:通过阳离子脂转染胺转染试剂,将pIRES-G2和pIRESneo质粒转移至SGC-7901细胞系。通过G418选择抗克隆。观察阳性克隆并使用吉姆萨染色计数。结果:(1)pIRES-G2组克隆数减少,克隆体积减少。 pIRESneo组细胞克隆数为87±3,pIRES-G2组细胞克隆数为53±4,占pIRESneo组的60.1%,差异有统计学意义(P <0.01,t = 15.45)。 (2)pIRES-G2在570 nm稳定转染获得的克隆细胞的平均吸光度为1.6966±0.2125,pIRESneo在570 nm稳定转染获得的克隆细胞的平均吸光度为2.1182±0.3675结论:细胞周期蛋白G2可以明显抑制SGC-7901细胞的增殖能力,可能是细胞周期调控的负调控因子。(P <0.01,t = 3.412)。

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