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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
其他题名Inhibitory Effect of Fluorocitrate on the Proliferation of Cultured Glioblastomas G422 Cells
瞿家桂1,2; 王正波2; 董锦润2; 马原野*2,3,4; yuaama0716@vip.sina.com
2008
发表期刊动物学研究
卷号29期号:4页码:427-430
合作性质其它
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(0.0025mmol/L,0.005mmol/L,0.01 mmol/L,0.025mmol/L和0.1 mmol/L)和作用时间(36h,48h和60h)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睃浓度的增加而增强;(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问的延长而增强:(3)低浓度(0.0025mmol/L和0.005mmol/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.
其他摘要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 36h, 48h and 60h after fluorocitrate (0.0025mmol/L, 0.005mmol/L, 0.01 mmol/L, 0.025mmol/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, 0.025mmol/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 0.005mmol/L). This study indicated that fluorocitrate inhibited the proliferation of glioma cells as a function of fluorocitrate concentration and treatment time.
关键词氟代柠檬酸 神经胶质瘤细胞 Mtt 增殖 抑制效应
资助者National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2) ; National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2) ; National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2) ; National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2)
收录类别其他
语种中文
资助者National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2) ; National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2) ; National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2) ; National Science Foundation of China (30470553, 30530270, 30670669, 30770700); 973 program (2005CB522803, 2007CB947703); 863 program (07013810, 2006AA02A116); the Major State Basic Research of China (2003CB716600); Chinese-Finnish International Collaboration Project-neuro (30621130076); Program of CASC (KSCXI-YW-R-33, YZ200737); National Key Technologies R&D Program; Yunnan Science and Technique Program (2006PT08-2)
文献类型期刊论文
条目标识符http://ir.kiz.ac.cn/handle/152453/921
专题认知障碍病理学
科研部门_神经系统编码(胡新天)
中国科学院昆明灵长类研究中心
通讯作者yuaama0716@vip.sina.com
作者单位1.中国科学技术大学生命科学学院,安徽合肥230026
2.中国科学院昆明动物研究所灵长类认知实验室,云南昆明650223
3.中国科学院昆明灵长类研究中心;云南昆明650223
4.昆明Biomed International,云南昆明650223
推荐引用方式
GB/T 7714
瞿家桂,王正波,董锦润,等. 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[J]. 动物学研究,2008,29(4):427-430.
APA 瞿家桂,王正波,董锦润,马原野*,&yuaama0716@vip.sina.com.(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.
MLA 瞿家桂,et al."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(2008):427-430.
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