实用肿瘤学杂志 ›› 2012, Vol. 26 ›› Issue (2): 119-124.doi: 10.3969/j.issn.1002-3070.2012.02.006

• 论著 • 上一篇    下一篇

红花多糖抑制PI3K/Akt信号通路诱导人胃癌细胞凋亡的研究

陶冀1, 黎清炜1, 石学魁3, 梁颖2, 王亚贤2   

  1. 1.哈尔滨医科大学附属第三医院肿瘤内科(哈尔滨 150081);
    2.黑龙江中医药大学微生物与免疫学教研室;
    3.牡丹江医学院微生物与免疫学教研室
  • 收稿日期:2011-10-18 出版日期:2012-04-28 发布日期:2014-12-03
  • 通讯作者: 王亚贤,E-mail:wangyxmail@yahoo.com.cn
  • 作者简介:陶冀,男,(1966-),主任医师,在读博士,从事肿瘤内科及肿瘤微创(氩氦刀)治疗
  • 基金资助:
    黑龙江省教育厅资助课题(11531119)

Safflower polysaccharides inhibit PI3K/Akt signaling pathway induces apoptosis of human gastric cancer cells

TAO Ji1,LI Qingwei1,SHI Xuekui3,LIANG Ying2,WANG Yaxian2   

  1. 1.Department of Internal Medicine,The Third Affiliated Hospital of Harbin Medical University,Harbin 150081;
    2.Heilongjing University of Chinese Medicine,Harbin 150040;
    3.Mudanjiang Medical College,Mudanjiang 157000
  • Received:2011-10-18 Online:2012-04-28 Published:2014-12-03

摘要: 目的 探讨红花多糖通过抑制PI3K/Akt信号通路调控胃癌细胞凋亡的机制。方法 MTT比色法观察SPS对人胃癌SGC-7901细胞体外增殖的抑制作用,流式细胞仪(FCM)分析细胞凋亡,实时荧光定量RT-PCR法和Western Blot法检测蛋白激酶B(Akt)基因及蛋白的表达情况。结果 红花多糖在一定范围内以剂量依赖方式和时间依赖方式抑制SGC-7901胃癌细胞生长。流式细胞仪检测,SGC-7901细胞经红花多糖处理24 h,其早期凋亡率、细胞坏死或晚期凋亡率显著增加,呈现明显的剂量依赖性。Real-time PCR和Western Blot检测发现,SPS处理的细胞Akt基因及蛋白表达量明显下降。结论 红花多糖对人胃癌SGC-7901细胞体外增殖具有明显的抑制作用,该抑制作用具有一定的时间依赖性和剂量依赖性;红花多糖能够下调Akt mRNA表达,降低Akt和p-Akt蛋白的表达量,抑制Akt通路发挥抗肿瘤作用。

Abstract: Objective To investigate how the safflower polysaccharides(SPS)regulate the apoptosis of human gastric cancer cell by inhibiting the PI3K/Akt signaling pathway.Methods We used MTT colorimetric method to observe the proliferation of human gastric cancer cell(SGC-790)in vitro and used flow cytometry(FCM)to analysis the apoptosis of the SGC-790 Cell.The expression of the protein kinase B(Akt)was detected by real-time quantitative RT-PCR and Western Blot,respectirely.Results SPS strongly inhibited gastric carcinoma cell line SGC-7901 to proliferate,and this inhibition relied on time and dosage conspicuously.Analyzed with flow cytometry,SGC-7901 cell treated with SPS for 24 hours showed increased percentage of early time apoptosis,cell necrosis and late time apoptosis,and took on dose dependence.Detected by real-time PCR and Western blot,expression of gene and protein of BCL-2 and Akt decreased and that of gene and protein of BAX increased in the cells treated with SPS.Conclusion SPS can inhibit human gastric carcinoma cell to proliferate,and this inhibition has time and dose dependence.SPS can cut down the expression of gene and protein of Akt.SPS restrain Akt pathways which may play antitumor function.

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