期刊文献+

白屈菜红碱对宫颈癌细胞的抑制作用研究 被引量:10

Inhibition Effects of Chelerythrine on Hela Cells
原文传递
导出
摘要 目的:研究白屈菜红碱(chelerythrine,CHE)对宫颈癌细胞(Hela)的增殖抑制作用,为CHE在预防和治疗宫颈癌方面提供实验依据。方法:不同浓度CHE作用于体外培养的Hela细胞后,采用台盼蓝拒染法和噻唑蓝(MTT)法研究白屈菜红碱对宫颈癌(Hela)细胞增殖能力的影响,流式细胞仪(FCM)检测细胞周期变化。结果:细胞接种密度越小、药物作用时间越长、药物浓度越大, CHE对Hela细胞的增殖抑制率越大,过大的细胞接种密度以及过低的药物浓度均不会引起明显的细胞死亡;CHE作用后的Hela细胞周期分布有明显变化,G1期细胞减少,S期和G2/M期细胞明显增多。结论:CHE在体外能明显抑制Hela细胞生长,其机理可能与CHE阻滞细胞周期、诱导细胞凋亡有关。 Objective: To study the inhibitory effects of CHE on Hela cells in vitro, and provide the theory basis for prevention and treatment of cervical cancer. Methods: Hela cells were treated with various concentration of CHE for 24, 36, 48 and 60 hours. The cell proliferation was estimated by the MTT assay. Distribution and apoptosis of the cell cycle were examined by Flow cytometry. The morphological change of the cells was observed with optical-microscope directly. Results: The growth of Hela cells has been significantly inhibited by CHE. The inhibition rate increases with the decrease of cell inoculums density, the increase of treating time and the increase of drug concentration. No evident death phenomenon was observed with excessive inoculums density or too low drug concentration. The cell cycle was redistributed: the Gl-phase cell fraction was decreased, while the S-phase and G2/M-phase cell fraction were significantly increased after treated with CHE. Conclusions: CHE can inhibit the growth of Hela cells, and the mechanism may be related to its blockage of cell cycle and apoptosis induction.
出处 《现代生物医学进展》 CAS 2009年第3期514-516,共3页 Progress in Modern Biomedicine
关键词 白屈莱红碱 宫颈癌细胞 抑制增殖 细胞周期 细胞凋亡 Chelerythrine Hela cell Proliferation inhibition Cell cycle Cell apoptosis
  • 相关文献

参考文献3

二级参考文献71

  • 1牛长群,何丽一.中药白屈菜的研究概况[J].中国药学杂志,1994,29(3):138-140. 被引量:15
  • 2Shao R G, Cao C X, Shimizu T, et al. Abrogation of an Sphase checkpoint and potentiation of camptothecin cytotoxicity by 7-hydroxystaurosporine (UCN-01) in human cancer cell lines, possibly influenced by p53 function [J]. Cancer Res, 1997, 57: 4029-4035.
  • 3Chmura S J, Dolan M E, Cha A, et al. In vitro and in vivo activity of protein kinase C inhibitor chelerythrine chloride induces tumor cell toxicity and growth delay in vivo [J]. Clin Cancer Res, 2000, 6: 737-742.
  • 4Hennequin C, Giocanti N, Favaudon V. Interaction of ionizing radiation with paclitaxel ( Taxol ) and docetaxel(Taxotere) in HeLa and SQ20B cells [J].Cancer Res, 1996,56: 1842-1850.
  • 5Zhang L, Wan X S, Donahue J J, et al. Effects of the Bowman-Birk inhibitor on clonogenic survival and cisplatin- or radiation-induced cytotoxicity in human breast, cervical, head,and neck cancer cells [J]. Nutr Cancer, 1999, 33: 165-173.
  • 6Vallejos R H, Rizzotto M G. Effect of chelerythrine on mitochondrial energy coupling [J]. FEBS Lett, 1972, 21 (2):195-198.
  • 7Wolff J, Knipling L. Antimicrotubule properties of benzophenanthridine alkaloids [J].Biochemistry, 1993, 32(48) :13334-13339.
  • 8Colombo ML, Bosisio E. Pharmacological activities of Chelidonium majus L.(Papaveraceae)[J].Pharmacol Res,1996,33(2):127-134.
  • 9Then M, Szentmihalyi K, Sarkozi A, et al. Effect of sample handling on alkaloid and mineral content of aqueous extracts of greater celandine (Chelidonium majus L.) [J]. J Chromatogr A,2000,889:69-74.
  • 10Joann LD, Sigmund SS. Comparative in vitro activity of sanguinarine against oral microbial isolates[J]. Antimicrob Agents Chemother,1985, 27(4): 663-665.

共引文献52

同被引文献121

引证文献10

二级引证文献72

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