Article Summary
孙龙和 夏建国 钱春华 汤民 钱明兰.白藜芦醇通过Pi3K/AKT 通路抑制胃癌SGC-7901 细胞增殖和迁移[J].现代生物医学进展英文版,2016,16(17):3637-3240.
白藜芦醇通过Pi3K/AKT 通路抑制胃癌SGC-7901 细胞增殖和迁移
Resveratrol Inhibit Gastric Carcinoma Cell SGC-7901 Proliferation andMigration by Inhibiting Pi3K/AKT Pathway
  
DOI:
中文关键词: 胃癌SGC-7901 细胞  白藜芦醇  Pi3K/AKT  增殖  迁移
英文关键词: SGC-7901 cell  Resveratrol  Pi3K/AKT  Proliferation  Migration
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Author NameAffiliation
孙龙和 夏建国 钱春华 汤民 钱明兰 南京医科大学泰州市第四人民医院普外科江苏省人民医院(南京医科大学第一附属医院)普外科 
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中文摘要:
      目的:验证白藜芦醇是否可以抑制胃癌SGC-7901 细胞增殖和迁移及其信号通路。方法:用不同浓度白藜芦醇干预 SGC-7901 细胞,再用LY-294002 和IGF-1 分别用来抑制和激活Pi3K/AKT 通路。MTT 法测细胞增殖,划痕试验和Transwell 试验 测细胞迁移,Western blot 检测细胞迁移相关蛋白(MMP-2、MMP-9)、细胞迁移相关蛋白(P21、P27)、以及AKT、p-AKT 的表达情 况;结果:相比于对照组,白藜芦醇组胃癌细胞增殖和迁移减弱(P=0.001),p-AKT表达减少(P<0.001);LY-294002 可以抑制p-AKT 的表达(P=0.004),和白藜芦醇一样可以抑制胃癌细胞的增殖和迁移;IGF-1 可以显著增加p-AKT的表达(P<0.001),可以逆转白藜 芦醇对胃癌细胞增殖和迁移的抑制作用。结论:白藜芦醇通过抑制Pi3K/AKT 信号通路抑制胃癌细胞增殖和迁移。
英文摘要:
      Objective:To verify whether resveratrol could inhibit SGC-7901 cells proliferation and migration through Pi3K/AKT pathway.Methods:Different concentrations of resveratrol were used to incubate with SGC-79011 cells. LY-294002 and IGF-1 were used to inhibit and activate Pi3K/AKT pathway respectively. MTT were used to investigate the proliferation of SGC-7901 cells. Transwell chambers and wound healing were employed to test the migratory ability of SGC-79011 cells. Western blotting were used to investigate the expressions of P21, P27, MMP-2, MMP-9, AKT and p-AKT inSGC-7901 cells.Results:Compared with the control group, the proliferation and migration of SGC-7901 cells and the expression of p-AKT were decreased in the resveratrol group (P=0.001); the inhibitory effect of the downregulation of p-AKT by LY-294002on the induction of SGC-7901 cells proliferation and migration was identical to that of resveratro (P<0.001); upregulation of p-AKT by IGF-1reversed the resveratrol-induced inhibition of SGC-7901 cells dedifferentiation (P<0.001).Conclusion:Resveratrol inhibits SGC-7901 cells proliferation and migration by suppressing Pi3K/AKT signaling pathway.
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