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雪灵芝水提物对人胃癌MGC-803细胞增殖及细胞周期的影响[J]. 肿瘤防治研究, 2013, 40(09): 821-825. DOI: 10.3971/j.issn.1000-8578.2013.09.001
引用本文: 雪灵芝水提物对人胃癌MGC-803细胞增殖及细胞周期的影响[J]. 肿瘤防治研究, 2013, 40(09): 821-825. DOI: 10.3971/j.issn.1000-8578.2013.09.001
Effects of Arenaria Kansuensis Aqueous Extract on Proliferation and Cell Cycle of Human Gastric Cancer Cell Line MGC-803[J]. Cancer Research on Prevention and Treatment, 2013, 40(09): 821-825. DOI: 10.3971/j.issn.1000-8578.2013.09.001
Citation: Effects of Arenaria Kansuensis Aqueous Extract on Proliferation and Cell Cycle of Human Gastric Cancer Cell Line MGC-803[J]. Cancer Research on Prevention and Treatment, 2013, 40(09): 821-825. DOI: 10.3971/j.issn.1000-8578.2013.09.001

雪灵芝水提物对人胃癌MGC-803细胞增殖及细胞周期的影响

Effects of Arenaria Kansuensis Aqueous Extract on Proliferation and Cell Cycle of Human Gastric Cancer Cell Line MGC-803

  • 摘要: 目的 探讨雪灵芝水溶性提取物(arenaria kansuensis aqueous extract,AKAE)对人胃癌细胞株MGC-803细胞增殖及细胞周期的影响。 方法 体外培养的MGC-803细胞经不同浓度AKAE处理,采用MTT法检测受试细胞增殖水平;应用流式细胞术检测AKAE处理12 h后各组细胞的细胞周期;Western blot检测不同浓度、不同时间AKAE处理组MGC-803细胞中cyclin D1蛋白表达水平;实时定量 PCR检测各组MGC-803细胞中cyclin D1、p16和p21基因的mRNA相对表达量。 结果 AKAE对体外培养的MGC-803细胞增殖具有浓度依赖性抑制作用(P<0.05),IC50为(0.134±0.005)mg/ml;经AKAE处理12 h,0.8 mg/ml组MGC-803细胞的 G1期细胞比例高于对照组、S期细胞比例低于对照组(P<0.05);(0.2~0.8) mg/ml浓度的AKAE处理,对MGC-803细胞中cyclin D1的蛋白及mRNA表达具有明显抑制作用(P<0.05);AKAE促进MGC-803细胞中p16、p21基因mRNA 表达,0.2 mg/ml处理组p16、p21 mRNA相对表达量分别为对照组的3.3倍和18.5倍。 结论 雪灵芝水提物(AKAE)对MGC-803细胞增殖具有抑制作用,其机制与G1期阻滞和对G1期相关因子表达的影响有关。

     

    Abstract: Objective To investigate the effects of arenaria kansuensis aqueous extract (AKAE) on proliferation and cell cycle of human gastric cancer cell line MGC-803. Methods MGC-803 cells were treated with AKAE at different concentration. The effect on proliferation of MGC-803 cells was detected by MTT assay. The flow cytometry was used to test the cell cycle of MGC-803 cells. The protein and mRNA expressions of cyclin D1, p16 and p21 in MGC-803 cells were detected by western blot and real-time PCR respectively. Results The proliferation of MGC-803 cells was dose-dependently inhibited by AKAE treatment in vitro(P<0.05),and the value of IC50 was (0.134±0.005)mg/ml. After treated with AKAE at the dose of 0.8 mg/ml for 12 h, the ratio of G1 phase in MGC-803 cell cycle was increased, and the ratio of S phase in MGC-803 cell cycle was decreased(P<0.05). The protein and mRNA expressions of cyclin D1 in MGC-803 cells were obviously blocked by AKAE at the dose of (0.2-0.8) mg/ml(P<0.05).AKAE treatment could enhance the mRNA expressions of p16 and p21 in MGC-803 cells.Compared with control group, the relative expression values of p16 and p21 mRNA in 0.2 mg/ml group were 2.30 and 17.5 times higher, respectively. Conclusion AKAE could inhibit the proliferation of MGC-803 cells, and the mechanism is closely associated with G1-phase cell cycle arrest and expression of G1-phase related factors.

     

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