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中国临床药理学与治疗学 ›› 2011, Vol. 16 ›› Issue (6): 621-626.

• 基础研究 • 上一篇    下一篇

维生素K2与苯那普利诱导胃癌细胞凋亡及抑制血管生成的体外实验研究

陈华1, 应卫星2, 李荣洲2   

  1. 1温州医学院附属第三医院肿瘤内科, 2消化内科,温州 325200,浙江
  • 收稿日期:2011-04-01 修回日期:2011-04-18 发布日期:2011-07-25
  • 通讯作者: 李荣洲,男,主任医师,研究方向:胃肠道肿瘤及消化内镜治疗。 Tel: 0577-65866220 E-mail: lirongzhou19761122@126.com
  • 作者简介:陈华,女,硕士,主治医师,研究方向:胃肠道肿瘤及肺癌。 Tel: 13958826132 E-mail: chenhua1215@126.com
  • 基金资助:
    浙江省医药卫生科学研究基金(2008B177);瑞安市科技局项目基金资助(20082081)

Combined treatment of vitamin K2 and benazepril induces apoptosis and inhibits angiogenesis on gastric cancer in vitro experiments

CHEN Hua1, YING Wei-xing2, LI Rong-zhou2   

  1. 1 Department of Oncology, 2 Department of Gastroenterology, the Third Affiliated Hospital of Wenzhou Medical College, Wenzhou 325000, Zhejiang, China
  • Received:2011-04-01 Revised:2011-04-18 Published:2011-07-25

摘要: 目的: 通过体外细胞培养观察维生素K2联合苯那普利对人胃癌SGC-7901细胞的影响,以探讨两者对胃癌细胞的影响及有无协同作用。方法: 通过人胃癌SGC-7901细胞培养,将处于对数生长期的SGC-7901细胞分成5组:药物组(维生素K2组、苯那普利组、联合组)、阴性对照组和空白对照组,阴性对照组不加药,空白对照组不加细胞。加入不同终浓度的药物(维生素K2: 5、10、20、40、80 μmol/L)或 (苯那普利: 0.625、1.25、2.5、5、10 μg/mL)或(维生素K2+苯那普利)。分别培养24、48和 72 h。利用MTT实验检测细胞生长抑制率,流式细胞仪Annexin V/PI双染法及梯状DNA电泳检测细胞凋亡情况,RT-PCR测定血管内皮生长因子(VEGF)表达。结果: 药物组能抑制胃癌SGC-7901细胞的增殖,且具有明显的剂量-效应关系,在抑制细胞增殖、诱导细胞凋亡及抑制VEGF表达方面,联合组较单独药物组作用更强。结论: 维生素K2与苯那普利联合有协同作用,能通过诱导细胞凋亡、抑制VEGF的表达抑制胃癌细胞增殖。

关键词: 维生素K2, 苯那普利, 细胞凋亡, 血管内皮生长因子, 胃癌

Abstract: AIM: To investigate the effect of vitamin K2 combined with benazepril on human gastric carcinoma SGC-7901 cells in vitro. METHODS: SGC-7901 cells at logarithmic growth phase were obtained and were divided into 5 groups: negative control group, blank control group, vitamin K2 therapy group, benazepril therapy group and combination therapy group(vitamin K2+benazepril). SGC-7901 cells were cultured with drugs of different concentrations (vitamin K2: 5, 10, 20, 40, 80 μmol/L)or benazepril (benazepril: 0.625, 1.25, 2.5, 5, 10 μg/mL) or vitamin K2+benazepril for 24, 48 and 72 h in drugs group. Cells cultured without drugs were served as negative control and blank control group without cells. The inhibition rates of SGC-7901 cells were detected by MTT assay, apoptosis rate of SGC-7901 cells was determined by Annexin V/PI double staining flow cytometry and DNA ladder, cell cycles of SGC-7901 cells were analysed by flow cytometry and VEGF expression of SGC-7901 cells were detected with RT-PCR. RESULTS: Vitamin K2 or benazepril had significant inhibitory effect on SGC-7901 cells growth, but combination group was more effective than the drug group alone on SGC-7901 cells proliferation, apoptosis and VEGF expression. CONCLUSION: Vitamin K2 combined with benazepril have obvious coordination therapeutic effect. The proliferation of SGC-7901 cells could be inhibited by inducing apoptosis and inhibiting VEGF expression.

Key words: Vitamin K2, Benazepril, Apoptosis, VEGF, Gastric carcinoma

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