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山东大学学报(医学版) ›› 2013, Vol. 51 ›› Issue (3): 21-26.

• 基础医学 • 上一篇    下一篇

EGCG抑制结肠癌HT-29细胞生长及血管生成的作用机制

辛玉1,袁俊华2,孙成刚1   

  1. 山东省卫生厅医药卫生发展计划项目(2009HZ066)
  • 收稿日期:2012-11-01 出版日期:2013-03-10 发布日期:2013-03-10
  • 通讯作者: 袁俊华(1972- ),女,博士,副主任医师,主要从事结肠癌的发病机制和早期诊治的研究.E-mail: yjh8005@163.com
  • 作者简介:辛玉(1987- ),女,硕士研究生,主要从事结肠癌的发病机制和早期诊治的研究。E-mail: xinyu8726@163.com
  • 基金资助:

    山东省卫生厅医药卫生发展计划项目(2009HZ066)

Mechanisms of EGCG inhibiting the proliferation of human colon cancer HT-29 cells and preventing angiogenesis

XIN Yu1,  YUAN Jun-hua2,  SUN Cheng-gang1   

  1. 1.Department of Gastroenterology;2.Department of Gastroenterology in healthcare building, 
    Provincial Hospital Affiliated to Shandong University,  Jinan 250021,  China
  • Received:2012-11-01 Online:2013-03-10 Published:2013-03-10

摘要:

目的   探讨表没食子儿茶素没食子酸酯( EGCG )对人结肠癌细胞HT-29生长的影响及抑制血管生成的相关机制。方法   EGCG(0、25、50、100μg /mL)作用于结肠癌细胞株HT-29 24h后, 采用MTT法检测EGCG对HT-29细胞生长的作用,应用RT-PCR及Western blot分别检测EGCG干预前后HT-29结肠癌细胞中TGFβ1、 15-PGDH、COX-2、VEGFmRNA及蛋白的表达情况。结果   MTT显示EGCG抑制HT-29细胞的生长,并随着浓度的增加及时间的延长抑制作用逐渐增强(P<0.05); TGF-β1、15-PGDH mRNA及蛋白表达量随着EGCG 浓度的增加而增加,COX-2、VEGF mRNA及蛋白表达量随着EGCG 浓度的增加而下降(P<0.05) 。结论   EGCG呈浓度及时间依赖性抑制HT-29细胞的增殖,可能通过诱导HT-29细胞中TGF-β1、15-PGDH, 抑制COX-2、VEGF mRNA及蛋白表达预防结肠癌的血管生成。

关键词: 结肠肿瘤;表没食子儿茶素没食子酸酯;转化生长因子β1;15-羟基前列腺素脱氢酶

Abstract:

Objective   To explore the mechanisms of epigallocatechin-3-gallate(EGCG) inhibiting the proliferation of human colon cancer HT-29 cells and preventing the angiogenesis in vitro. Methods   In vitro,  human colon cancer cell line HT-29 was treated by EGCG in various concentrations(0, 25,  50,  100μg /mL) for 24h. The inhibitory effect of proliferation was assayed by MTT method. The mRNA and protein expressions of transforms growth factorsβ1(TGF-β1),  15-hydroxyprostaglandin dehydrogenase (15-PGDH),  cyclooxygenase-2(COX-2)and vascular endothelial growth factor(VEGF) in human colon cancer cell line HT-29 were respectively examined by RT-PCR and Western blot. Results   MTT assay showed that EGCG inhibited HT-29 cells in a dose-and-time dependent manner(P<0.05). It was found that the expressions of TGF-β1 and 15-PGDH mRNA and protein  were up-regulated and COX-2 and VEGF were down-regulated,  both in a dose-dependent manner(P<0. 05). Conclusion   EGCG inhibits the proliferation of HT-29 cells in a dose-and-time dependent manner. EGCG possibly prevents angiogenesis of HT-29 cells via activating TGF-β1/15-PGDH pathways and inhibiting COX-2 and VEGF pathways in a dose-dependent manner.

Key words: Colonic neoplasms; Epigallocatechin-3-gallate; Transforms growth factorsβ1; 15-Hydroxyprostaglandin dehydrogenase

中图分类号: 

  • R574.62
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