第四军医大学学报2009,Vol.30Issue(14) :1289-1291.

2-(3-羧基-1-丙酰氨基)-2-脱氧-D-葡萄糖诱导人结肠癌SW1116凋亡的作用

Experimental study on apoptosis of human colon carcinoma cell line SW1116 induced by 2-[(3-carboxy-1-oxoprogy1) amino]-2-deoxy-D-Glucose

寇炜 吴静 赵晋 兰咏梅 窦春江 王爱勤
第四军医大学学报2009,Vol.30Issue(14) :1289-1291.

2-(3-羧基-1-丙酰氨基)-2-脱氧-D-葡萄糖诱导人结肠癌SW1116凋亡的作用

Experimental study on apoptosis of human colon carcinoma cell line SW1116 induced by 2-[(3-carboxy-1-oxoprogy1) amino]-2-deoxy-D-Glucose

寇炜 1吴静 2赵晋 1兰咏梅 1窦春江 1王爱勤3
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作者信息

  • 1. 西北民族大学医学院技能教研室,甘肃,兰州,730030
  • 2. 北京大学第九临床医院消化科,北京,100038
  • 3. 中国科学院兰州化学物理研究所,甘肃,兰州,730000
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摘要

目的:研究D-葡萄糖衍生物2-(3-羧基-1-丙酰氨基)-2-脱氧-D-葡萄糖(COPADG)对人结肠癌SW1116细胞生长增殖的影响,进而探讨COPADG诱导SW1116细胞凋亡的作用.方法:用不同浓度的COPADG处理SW1116,采用MTT法测定其对SW1116细胞生长增殖的抑制作用,通过DNA琼脂糖凝胶电泳、流式细胞术观察其对SW1116细胞诱导凋亡的效应.结果:COPADG能抑制SW1116细胞的生长增殖,并呈一定的浓度、时间依赖性;COPADG能诱导结肠癌SW1116细胞凋亡;DNA琼脂糖凝胶电泳呈现典型的DNA梯形条带图谱;流式细胞仪检测出现典型的亚二倍体凋亡峰.结论:COPADG在体外可显著诱导结肠癌SW1116细胞凋亡.

Abstract

AIM: To investigate the effect of 2-[(3-carboxy-1-oxoprogy1)amino]-2-deoxy-D-Glucose (COPADG) on human colon carcinoma cell line SW1116 and to study the function of the COPADG in inducing cell line SW1116 apoptosis. METHODS: SW1116 cells were treated with the COPADG at various concen-trations. WIT assay was used to examine the growth and prolifera-tion of SW1116 cells after treatment with the COPADG. Agarose gel electrophoresis of DNA fragmentation and flow cytometry were used to analyze the cell line SW1116 apoptosis. RESULTS: COPADG significantly inhibited the growth and proliferation of cell line SW1116 in a dose- and time-dependent manner. Agarose gel electrophoresis analysis revealed DNA ladder and atypical sub-diploid peak was observed by flow cytometry. CONCLUSION: COPADG may inhibit SW1116 cell growth and proliferation through inducing apoptosis.

关键词

2-(3-羧基-1-丙酰氨基)-2-脱氧-D-葡萄糖/细胞凋亡/SW1116细胞

Key words

2-[(3-carboxy-1-oxoprogy1) amino ]-2-deoxy-d-glucose/apoptosis/SW1116 cells

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基金项目

西北民族大学中青年科研项目(D2004-021)

出版年

2009
第四军医大学学报
第四军医大学

第四军医大学学报

CSTPCDCSCD北大核心
影响因子:0.599
ISSN:1000-2790
被引量1
参考文献量5
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