世界中医药
文章摘要
引用本文:韦小白 董竞成.黄芩苷对人肺腺癌LTEP-A2细胞的抑制作用及机制研究[J].世界中医药,2014,9(02):.  
黄芩苷对人肺腺癌LTEP-A2细胞的抑制作用及机制研究
Study on Inhibition Effect and Mechanism of Baicalin on LTEP-A2 Cells in Lung Cancer Patients
投稿时间:2013-10-10  
DOI:10.3969/j.issn.1673-7202.2014.02.025
中文关键词:  黄芩苷  增值  迁移  LTEP-A2细胞  MMP-2  MMP-9
English Keywords:Baicalin  Proliferation  Metastasis  LTEP-A2 cells  MMP-2  MMP-9
基金项目:
作者单位
韦小白 董竞成 1 复旦大学附属华山医院静安分院,上海,200040
2 复旦大学附属华山医院,上海,200040 
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中文摘要:
      目的:研究观察黄芩苷对人肺腺癌LTEP-A2细胞株体外的抑制作用及相关机制。方法:采用不同浓度的黄芩苷干预人肺腺癌LTEP-A2细胞株,用CCK-8方法检测不同时间点不同浓度的黄芩苷对肺癌细胞增殖的抑制程度,接着用细胞划痕试验和Transwell小室侵袭试验观察黄芩苷对肺癌细胞体外迁移、侵袭能力的影响;用Western blot进一步检测黄芩苷干预后肺癌细胞MMP-2、MMP-9、TGF-β的表达的变化。结果:黄芩苷能明显抑制肺癌细胞增殖;能不同程度降低肺癌细胞的迁移、侵袭、体外划痕愈合能力,呈浓度依赖性;黄芩苷能不同程度下调MMP-2、MMP-9表达,其中以高浓度效果明显,中浓度居中,低浓度作用稍弱,与空白对照组比较,组间差异有统计学意义,P<0.05;对肺癌细胞TGF-β的表达没有显著影响,与对照组比较,P>0.05。结论:黄芩苷能不同程度地降低肺癌增殖迁移侵袭的能力,其机制可能是通过下调MMP-2、MMP-9的表达从而对肺癌细胞的增殖、迁移、侵袭发挥抑制作用。
English Summary:
      To explore the inhibition effects and mechanism of baicalin on LTEP-A2 cells in vitro of lung cancer patients.Methods:Human pneumonicadenocarcinoma cell line LTEP-A2 was cultured with different dose of baicalin for different periods of time. Cell proliferation was assayed by using Cell Counting Kit-8, and further in vitro study including tumor cell migration and invasion, wound healing assays were performed. Besides ,MMP-2,MMP-9,TGF-β,which were related to the migration and metastasis potential in lung cancer cell lines were detected by western blot.Results:Baicalin inhibited the proliferation of LTEP-A2 cells in a time and concentration-dependent manner. In tumor cell migration and invasion test, wound healing assays etc. showed significantly decreased migration, invasion in baicalin-treated cell groups vs control tumor cells. Further study showed that MMPs decreased after baicalin-treated. The higher doses of baicalin, the lower level of MMP-2/MMP-9.However, baicalin did not have a significant effect on the TGF-β. Conclusion:Baicalin inhibits the proliferation and migration of lung cancer LTEP-A2 cells, possibly by decreasing the expression of MMP-2, MMP-9 in part.
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