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首页> 外文期刊>World Journal of Gastroenterology >Effect of cyclin G2 on proliferative ability of SGC-7901 cell
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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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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 done 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:用阳离子脂质体转染试剂将pIRES-G2和pIRESneo质粒转入SGC-7901细胞株。通过G418选择抗克隆。观察阳性克隆并使用吉姆萨染色计数。通过MTT测定细胞增殖能力。结果:(1)pIRES-G2组的完成数量减少,克隆量减少。 pIRESneo组细胞克隆数为87±3,pIRES-G2组为53±4,占pIRESneo组的60.1%,差异有统计学意义(P <0.01,t = 15.45)。 (2)通过pIRES-G2在570nm处稳定转染获得的克隆细胞的平均吸光度为1.6966±0.2125,通过pIRESneo在570nm处稳定转染获得的克隆细胞的平均吸光度为2.1182±0.3675。两者之间的差异(P <0.01,t = 3.412)。结论:Cyclin 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。

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