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瞿家桂, 王正波, 董锦润, 马原野. 2008: 氟代柠檬酸对体外培养的神经胶质瘤细胞G422增殖的抑制效应. 动物学研究, 29(4): 427-430. DOI: 10.3724/SP.J.1141.2008.04427
引用本文: 瞿家桂, 王正波, 董锦润, 马原野. 2008: 氟代柠檬酸对体外培养的神经胶质瘤细胞G422增殖的抑制效应. 动物学研究, 29(4): 427-430. DOI: 10.3724/SP.J.1141.2008.04427
QU Jia-gui, WANG Zheng-bo, DONG Jin-run, MA Yuan-ye. 2008. Inhibitory Effect of Fluorocitrate on the Proliferation of Cultured Glioblastomas G422 Cells. Zoological Research, 29(4): 427-430. DOI: 10.3724/SP.J.1141.2008.04427
Citation: QU Jia-gui, WANG Zheng-bo, DONG Jin-run, MA Yuan-ye. 2008. Inhibitory Effect of Fluorocitrate on the Proliferation of Cultured Glioblastomas G422 Cells. Zoological Research, 29(4): 427-430. DOI: 10.3724/SP.J.1141.2008.04427

氟代柠檬酸对体外培养的神经胶质瘤细胞G422增殖的抑制效应

Inhibitory Effect of Fluorocitrate on the Proliferation of Cultured Glioblastomas G422 Cells

  • 摘要: 为研究氟代柠檬酸(Fluorocitrate)对体外培养的神经胶质瘤细胞生长的影响,采用MTT法研究不同的氟代柠檬酸浓度(0.0025 mmol/L,0.005 mmol/L,0.01 mmol/L,0.025 mmol/L和0.1 mmol/L)和作用时间(36 h,48 h和60 h)对神经胶质瘤细胞G422增殖的影响。结果发现:(1)氟代柠檬酸可抑制G422细胞的增殖,并且其抑制作用随氟代柠檬酸浓度的增加而增强;(2)高浓度(0.01 mmol/L,0.025 mmol/L和0.1 mmol/L)氟代柠檬酸对G422细胞的增殖抑制作用随作用时间的延长而增强;(3)低浓度(0.0025 mmol/L和0.005 mmol/L)氟代柠檬酸对G422细胞的增殖抑制作用不随作用时间的延长而改变。实验表明,氟代柠檬酸能够抑制神经胶质瘤细胞的增殖,其抑制能力随氟代柠檬酸浓度的增加和作用时间的延长而加强。

     

    Abstract: In the present study, the effects of fluorocitrate on the proliferation of cultured glioblastomas G422 cells were investigated. Proliferation of glioblastomas G422 cells was measured by MTT assay at 36 h, 48 h and 60 h after fluorocitrate (0.0025 mmol/L, 0.005 mmol/L, 0.01 mmol/L, 0.025 mmol/L and 0.1 mmol/L) treatment. Our results showed that: (1) Fluorocitrate inhibited the proliferation of glioblastomas G422 cells in a dose dependent manner; (2) The inhibition rate increased with treatment time at high concentrations of fluorocitrate (0.01 mmol/L, 0.025 mmol/L and 0.1 mmol/L); (3) The inhibition rate did not increase with treatment time at low concentrations of fluorocitrate (0.0025 mmol/L and 0.005 mmol/L). This study indicated that fluorocitrate inhibited the proliferation of glioma cells as a function of fluorocitrate concentration and treatment time.

     

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