期刊文献+

人参皂甙肠道代谢物CompoundK对人胃癌细胞增殖及凋亡相关基因表达的影响 被引量:1

Compound K induced apoptosis of gastric carcinoma cells and the effect on expression of apopto-sis-related genes
原文传递
导出
摘要 目的观察人参皂甙肠道代谢物CompoundK(CK)对人胃癌细胞BGC823细胞增殖、凋亡的影响。方法实验分组:对照组(PBS溶液),实验组(浓度分别为2.5、5、7.5、10μmol/L)。噻唑蓝(MTT)比色法分别检测CK作用于细胞后其活力及生长抑制率;流式细胞术检测CK作用后细胞周期时相、凋亡率;免疫印迹法(Westernblot)检测凋亡相关蛋白的表达。结果5μmol/LCK作用细胞48h时,细胞生长周期阻滞于G2/M期,细胞凋亡率为(21.17±3.16)%;Westernblot检测显示Bcl-2,Bid蛋白表达随着药物浓度的增加而减少,Fas和Fas—L蛋白表达量却没有明显变化。结论CK是通过线粒体介导的凋亡通路途径来诱导人胃癌细胞发生凋亡的。 Objective To investigate the effect of CK on proliferation, apoptosis of BGC823 cells. Methods BGC823 cells were treated with CK at different concentrations, cell viability was as-sayed using MTT methods. Cell cycle, apoptosis rate were assayed by flow cytometry. The expression of apoptosis-related protein were detected by Western blotting. Results After BGC823 cells were treated with 5 μmol/L CK for 48 h, the growth cycle was arrested on G2/M phase, the apoptosis rate was (21.17 ± 3.16)%. The expressions of Bcl-2, Bid protein was down-regulal the Fas and Fas-L protein were not significantly changed. Conclusions BGC823 cells, and induces apoptosis via mitochondrion-mediated pathway Lted after CK treatment, while CK inhibits proliferation of BGC823 cells, and induces apoptosis via mitochondrion-mediated pathway.
出处 《中国实用医刊》 2014年第5期12-14,共3页 Chinese Journal of Practical Medicine
关键词 COMPOUND K 胃癌 细胞凋亡 Compound K Gastric carcinoma Cell apoptosis
  • 相关文献

参考文献7

  • 1Choi K,Kim M,Ryu J. Ginsenosides compound K and Rh(2) inhibit tumor necrosis factor-alpha-induced activation of the NF-kappaB and JNK pathways in human astroglial cells[J].Neuroscience Letters,2007,(01):37-41.
  • 2Shin YW,Bae EA,Kim SS. Effect of ginsenside Rb1 and compound K in chronic oxazolone-induced mouse dermatitis[J].International Journal of Immunopharmacology,2005,(7-8):1183-1191.
  • 3Yoon SH,Han E J,Sung JH. Anti-diabetic effects of compound K versus metformin versus compound K-metformin combination therapy in diabetic db/db mice[J].Biological and Pharmaceutical Bulletin,2007,(11):2196-2200.
  • 4Kim do Y,Yuan HD,Chung IK. Compound K,intestinal metabolite of ginsenoside,attenuates hepatic lipid accumulation via AMPK activation in human hepatoma cells[J].Journal of Agricultural and Food Chemistry,2009,(04):1532-1537.
  • 5Chae S,Kang KA,Chang WY. Effect of compound K,a metabolite of ginseng saponin,combined with gamma-ray radiation in human lung cancer cells in vitro and in vivo[J].Journal of Agricultural and Food Chemistry,2009,(13):5777-5782.
  • 6Choo MK,Sakurai H,Kim DH. A ginseng saponin metabolite suppresses tumor necrosis factor-alpha-promoted metastasis by suppressing nuclear factor-kappaB signaling in murine colon cancer cells[J].Oncology Reports,2008,(03):595-600.
  • 7Jung SH,Woo MS,Kim SY. Ginseng saponin metabolite suppresses phorbol eater-induced matrix metalloproteinase-9 expression through inhibition of activator protein-1 and mitogen-activated protein kinase signaling pathways in human astroglioma cells[J].International Journal of Cancer,2006,(02):490-497.

同被引文献26

引证文献1

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部