摘要:ABSTRACT:Objective To investigate the inhibitory effect of 11,12-didehydro-3,19-cyclophos-phate andrographolide on the proliferation,invasion and migration of gastric cancer SGC7901 cells and its mechanism of action.Methods SGC7901 cells were treated with 11,12-didehydro-3,19-cy-clophosphate andrographolide (20,40,60,80 and 100 μmol·L-1 )for 24,48 and 72 hours,respec-tively.Control cells received the vehicle only.Cell proliferation and viability were measured by MTT assay.After treatment for 24 hours,invasion assay was conducted using transwell cham-bers.After treatment for 48 hours,the expression of cell proliferation and migration-related pro-teins Akt,p-AKT,JNK,p-JNK,MMP-2 and MMP-9 was detected by Western blot.Results Compared with control group,11,12-didehydro-3,19-cyclophosphate andrographolide treatment significantly inhibited the proliferation of SGC7901 cells in a time- and concentration-dependent manner (P <0.01).Furthermore,treatment with 11,12-didehydro-3,19-cyclophosphate androgra-pholide (40 μmol·L-1 )significantly decreased the migration and invasion of SGC7901 cells,com-pared with control group(P <0.01).Moreover,treatment with 11,12-didehydro-3,19-cyclophos-phate andrographolide (40 μmol · L-1 )for 48 hours significantly reduced the expression of p-AKT,p-JNK,MMP-2 and MMP-9,compared with control group.Conclusion The treatment with 11,12-didehydro-3,19-cyclophosphate andrographolide can decrease the proliferation,inva-sion and migration of gastric cancer SGC7901 cells through inhibiting the expression of p-AKT,p-JNK,MMP-2 and MMP-9 proteins.%目的:研究脱水穿心莲内酯衍生物[11,12-脱水-二(2-氯乙基)氨基-3,19-环磷酸酯穿心莲内酯]抑制胃癌SGC7901细胞增殖、侵袭及迁移的作用,并探讨其可能的作用机制。方法取 SGC7901细胞,加入11,12-脱水-二(2-氯乙基)氨基-3,19-环磷酸酯穿心莲内酯中,分别设置20、40、60、80和100μmol· L-15个药物浓度组;不加11,12-脱水-二(2-氯乙基)氨基-3,19-环磷酸酯穿心莲内酯的单纯细胞为空白对照组,分别置于培养箱孵育24、48、72 h;采用 MTT 法检测细胞增殖与细胞活力;采用 Transwell 小室测定24 h 后 SGC7901细胞的侵袭能力,并通过蛋白免疫印迹(Western blot)法检测48 h 细胞增殖与迁移相关蛋白 Akt、p-AKT、JNK、p-JNK、MMP-2、MMP-9的表达情况。结果与空白对照组相比:20、40、60、80和100μmol·L-15个药物浓度组能明显抑制 SGC7901细胞增殖,并呈时间和浓度依赖性(P <0.01)。空白对照组迁移和侵袭能力无显著变化,11,12-脱水-二(2-氯乙基)氨基-3,19-环磷酸酯穿心莲内酯(40μmol·L-1组)处理 SGC7901细胞迁移和侵袭能力较空白对照组明显减弱(P <0.01)。采用11,12-脱水-二(2-氯乙基)氨基-3,19-环磷酸酯穿心莲内酯(40μmol·L-1)处理 SGC7901细胞48 h后,可明显抑制 p-AKT、p-JNK、MMP-2及 MMP-9的表达水平。结论11,12-脱水-二(2-氯乙基)氨基-3,19-环磷酸酯穿心莲内酯可降低胃癌 SGC7901细胞的增殖、侵袭和迁移能力,其作用机制可能是通过抑制 p-AKT、p-JNK、MMP-2、MMP-9蛋白的表达。