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首页|期刊导航|广东医学|人参皂苷 Rg3对人鼻咽癌 CNE -2细胞血管生成拟态及迁移能力的影响

人参皂苷 Rg3对人鼻咽癌 CNE -2细胞血管生成拟态及迁移能力的影响

孔霞 尚九龙 周艳芳 王槐高 顾帝水

广东医学Issue(9):1314-1317,4.
广东医学Issue(9):1314-1317,4.

人参皂苷 Rg3对人鼻咽癌 CNE -2细胞血管生成拟态及迁移能力的影响

20(R)- ginsenoside Rg3 inhibits vasculogenic mimicry and cell migration of human nasopharyngeal carcinoma CNE-2 cell line in vitro

孔霞 1尚九龙 2周艳芳 1王槐高 1顾帝水1

作者信息

  • 1. 广东医学院病理生理学教研室 广东东莞 523808
  • 2. 广东医学院生理学教研室 广东东莞 523808
  • 折叠

摘要

Abstract

Objective To study the inhibitory effects of 20(R)- ginsenoside Rg3 on vasculogenic mimicry and migration of human nasopharyngeal carcinoma CNE - 2 cell line in vitro. Methods CNE - 2 cells treated with different concentrations of Rg3(0 μmol·L - 1 ,38 μmol·L - 1 ,76 μmol·L - 1 and 114 μmol·L - 1 )were assayed with transwell assay and anti - angiogenic test for testing the potential of migration and tube - like structure(TLSs)formation,respec-tively. Meanwhile,the expression of COX - 2,HIF - 1α,VEGF and Fascin1 proteins were detected by Western blotting. Results The formation of TLSs in CNE - 2 cells were significantly inhibited by Rg3 in concentration dependent manners (P < 0. 01);so was the migration ability of CNE - 2 cells(P < 0. 05). At the same time,the expression of COX - 2, HIF - 1α,VEGF and Fascin1 in CNE - 2 cells were down - regulated by Rg3. A significantly positive correlation between the expression of Fascin1 and the migration ability was observed(P < 0. 05),so was the significantly positive correlation between the expression of COX - 2,HIF - 1α and VEGF and the inhibition of the TLS formation(P < 0. 05). Conclusion Rg3 can inhibit the vasculogenic mimicry and migration of CNE - 2 cells in vitro,via the down - regulation of COX - 2, HIF - 1α,VEGF and Fascin1.

关键词

人参皂苷Rg3/鼻咽癌/血管生成拟态/细胞迁移

Key words

20(R)- Ginsenoside Rg3/Nasopharyngeal carcinoma/Vasculogenic mimicry/Cell migration

引用本文复制引用

孔霞,尚九龙,周艳芳,王槐高,顾帝水..人参皂苷 Rg3对人鼻咽癌 CNE -2细胞血管生成拟态及迁移能力的影响[J].广东医学,2015,(9):1314-1317,4.

基金项目

广东省中医药管理局建设中医药强省科研课题(编号20122082),广东省医学科研基金资助项目(编号B2011235),广东省东莞市高等院校科研计划项目(编号200910815267),广东省湛江市科技攻关项目(编号2009C3101013),广东医学院面上项目资助课题 ()

广东医学

OA北大核心CSTPCD

1001-9448

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