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国产雷帕霉素对人淋巴瘤细胞Raji增殖的影响[J]. 肿瘤防治研究, 2012, 39(02): 157-160. DOI: 10.3971/j.issn.1000-8578.2012.02.010
引用本文: 国产雷帕霉素对人淋巴瘤细胞Raji增殖的影响[J]. 肿瘤防治研究, 2012, 39(02): 157-160. DOI: 10.3971/j.issn.1000-8578.2012.02.010
Effect of Rapamycin in Proliferation of Human Burkitt Lymphoma Cells[J]. Cancer Research on Prevention and Treatment, 2012, 39(02): 157-160. DOI: 10.3971/j.issn.1000-8578.2012.02.010
Citation: Effect of Rapamycin in Proliferation of Human Burkitt Lymphoma Cells[J]. Cancer Research on Prevention and Treatment, 2012, 39(02): 157-160. DOI: 10.3971/j.issn.1000-8578.2012.02.010

国产雷帕霉素对人淋巴瘤细胞Raji增殖的影响

Effect of Rapamycin in Proliferation of Human Burkitt Lymphoma Cells

  • 摘要: 目的 探讨国产雷帕霉素(宜欣可)对人淋巴瘤细胞株Raji细胞体外生长及对mTOR/p 70S6K信号通路的影响。方法MTT法检测不同浓度(0、1、5、10、20、40、50、100 nmol/L)国产雷帕霉素作用不同时间(24、48、72 h)对Raji 细胞增殖的影响。光学显微镜观察Raji细胞形态学变化。流式细胞仪测定国产雷帕霉素对Raji细胞周期分布和凋亡的影响。Western blot 方法检测国产雷帕霉素处理前后对Raji 细胞mTOR、p70S6K、p-p70S6K蛋白的影响。结果国产雷帕霉素对Raji细胞增殖有明显的抑制作用(不同浓度P<0.01或P<0.05),呈现明显的剂量-效应和时间-效应依赖关系。国产雷帕霉素明显抑制Raji细胞周期发展(P<0.05),但没有发生明显的凋亡(P>0.05)。0、10、50、100 nmol/L国产雷帕霉作用于Raji细胞的mTOR、p-p70S6K,其蛋白量随药物浓度增大而降低(P<0.05),p70S6K随药物浓度增大而升高(P<0.05)。结论人淋巴瘤细胞株Raji中存在mTOR/p70S6K信号通路激活状态,宜欣可可抑制该通路激活并通过阻滞细胞周期发展抑制Raji细胞增殖。

     

    Abstract: Objective To investigate rapamycin effects on growth inhibition and mTOR/p70S6K signaling pathway of human Burkitt lymphoma cell line Raji cells. Methods Proliferations of Raji cells under different of concentrations (0,1,5,10,20,40,50 and 100nmol/L) and different times (24,48 and 72 h) were investigated by MTT assay.Apoptosis and cell cycle were analyzed via flowcytometry.The morphological alterations were confirmed by the optical microscope.The expressions of mTOR,p70S6K,p-p70S6K proteins were examined by Western blot technique in the rapamycin-treated and untreated Raji cells. Results Rapamycin inhibited the proliferation of Raji cells at concentrations more than 5nmol/L(P<0.05),in a dose and time dependent manner.After treatment with rapamycin,the number of cells at S phase and G2/M phase was decreased gradually (P<0.05),but significantly increased at G0/G1 phase in dose and time dependent manners (P<0.05).However,evident apoptosis did not observed in Raji cells.The expression of mTOR、p-p70S6K proteins was decreased gradually while the expression of p70S6K protein was increased in a concentration-dependent manner (P<0.05). Conclusion mTOR/p70S6K signaling pathway was constitutively activated in Raji cells and Rapamycin inhibited Raji cell proliferation by arrest at G0/G1 phase and inhibition of mTOR/p70S6K signaling pathway.

     

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