期刊文献+

β-榄香烯对人食管癌细胞Eca-109增殖、凋亡和迁移的影响 被引量:3

Effect of β-elemene on proliferation,apoptosis and migration in human esophageal carcinoma cell Eca-109
下载PDF
导出
摘要 目的检测β-榄香烯对人食管鳞癌细胞Eca-109增殖、凋亡和迁移的影响,初步探讨其对食管癌细胞的作用机制。方法采用不同浓度的β-榄香烯(终浓度分别为0μg/m L、1μg/m L、20μg/m L、100μg/m L、200μg/m L、400μg/m L、600μg/m L)作用于Eca-109细胞后,CCK-8测定细胞增殖活力。同时采用Annexin V/PI双染法(β-榄香烯作用浓度为0μg/m L、10μg/m L、100μg/m L)检测细胞的凋亡率(流式细胞仪)。此外,采用β-榄香烯(0μg/m L、100μg/m L)作用细胞后,检测其对细胞迁移的影响(榄香烯浓度为0μg/m L组作为对照组)。β-榄香烯作用于细胞均为48 h。结果β-榄香烯孵育48 h后对食管癌细胞增殖抑制在不同浓度之间比较,差异均有统计学意义(P<0.05),同时,随着浓度增加,β-榄香烯对细胞的增殖抑制进一步增强,且其抑制作用存在剂量依赖性;不同浓度β-榄香烯对细胞的凋亡率间比较,差异均有统计学意义(P<0.05);相对于对照组,β-榄香烯显著降低迁移细胞数,两者间差异亦有统计学意义(P<0.05)。结论β-榄香烯显著抑制了Eca-109细胞的增殖活力,且其抑制存在剂量依赖性,同时可诱导凋亡及抑制细胞迁移,可能通过诱导细胞凋亡及抑制迁移发挥其抗肿瘤效应。 Objective To investigate the effect of β-elemene on the proliferation, apoptosis and migration of hu-man esophageal squamous carcinoma cell Eca-109, and to explore its mechanism of anti-tumor effect. Methods Eca-109cells were incubated with different concentrations of β-elemene (final concentration to 0 μg/mL, 1 μg/mL, 20 μg/mL,100 μg/mL, 200 μg/mL, 400 μg/mL, 600 μg/mL) for 48 h, then cholecystokinin octapeptide (CCK-8) assay was used to de-tect the cell proliferation activity. For the apoptosis detection, Annexin-V/PI assay was used and the cells were detectedon the flow cytometry before incubation with different concentrations of β-elemene (final concentration to 0 μg/mL,10 μg/mL and 100 μg/mL). While for the migration activity detection, the concentration of 0 μg/mL and 100 μg/mL ofβ-elemene were set as the control and experimental group respectively. Results After the incubation of 48 h for β-el-emene, the inhibition of cell proliferation were significant different among different concentrations of β-elemene (P〈0.05).Meantime, with the increase of concentration, the inhibition of cell proliferation was further enhanced by β-elemene, andits inhibitory effect was dose-dependent. The cell apoptosis were significant different among different concentrations ofβ-elemene (P〈0.05). Compared with the control group, β-elemene significantly reduced the number of migratory cells (P〈0.05). Conclusion The proliferation of cell line of Eca-109 can be inhibited by β-elemene and the inhibited rate isdose-dependent. β-elemene may make its anti-tumor effect through inducing the cell apoptosis and migration.
出处 《海南医学》 CAS 2018年第8期1037-1043,共7页 Hainan Medical Journal
基金 广东省中医药局基金项目(编号:20161186) 广东省番禺区珠江科技新星专项资助项目(编号:2013-专15-6.10)
关键词 食管癌 Β-榄香烯 增殖抑制 凋亡 迁移 Esophageal carcinoma β-elemene Proliferation inhibition Apoptosis Migration
  • 相关文献

参考文献3

二级参考文献28

  • 1CURCIO A, TORELLA D, INDOLFI C. Mechanisms of smooth muscle cell proliferation and endothelial regeneration after vascular injury and stenting: approach to therapy [ J]. Circ J, 2011, 75 (6) : 1287 -1296.
  • 2ERNST M C, SINAL C J. Chemerin: at the crossroads of inflam- mation and obesity [ J]. Trends Endocrinol Metab, 2010, 21 ( 11 ) : 660 - 667.
  • 3SPIROGLOU S G, KOSTOPOULOS C G, VARAKIS J N, Papada- ki HH. Adipokines in periaortic and epicardial adipose tissue: dif- ferential expression and relation to atherosclerosis[J]. J Athern- scler Thromb, 2010, 17(2) : 115 - 130.
  • 4DONG B, JI W, ZHANG Y. Elevated serum chemerin levels are associated with the presence of coronary artery disease in patients with metabolic syndrome[J]. Intern Med, 2011, 50(10) : 1093 - 1097.
  • 5DONG S, XIONG W, YUAN J, et al. MiRNA - 146a regulates the maturation and differentiation of vascular smooth muscle cells by targeting NF - κB expression[ J ]. Mol Med Rep, 2013,8 (2) : 407 -412.
  • 6MATTERN A, ZELLMANN T, BECK SICKINGER A G. Process- ing, signaling, and physiological function of chemerin [ J ]. IUB- MB Life, 2014, 66(1) : 19 -26.
  • 7ROMAN A A, PARLEE S D, SINAL C J. Chemerin: a potential endocrine link between obesity and type 2 diabetes [ J ]. Endo- crine, 2012, 42(2) : 243 -251.
  • 8WEIGERT J, NEUMEIER M, WANNINGER J, et al. Systemic chemerin is related to inflammation rather than obesity in type 2 di- abetes[J]. Clin Endoerinol, 2010, 72 (3) : 342 - 348.
  • 9KAUR J, ADYA R, TAN B K, et al. Identification of chemerin receptor ( ChemR23 ) in human endothelial ceils : ehemerin - in- duced endothelial angiogenesis [ J]. Biochem Biophys Res Com- mun, 2010, 391(4) : 1762 -1768.
  • 10YOO H J, CHOI H Y, YANG S J, et al. Circulating chemerin level is independently correlated with arterial stiffness[ J]. J Ath- eroscler Thromb, 2012, 19(1): 59-68.

共引文献6

同被引文献77

引证文献3

二级引证文献18

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