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作 者:倪洪早 张芸[1] 崔晨晨[1] 朱一硕 陈洪福[1] 范月超[1] 郑骏年[1]
出 处:《中华实验外科杂志》2016年第4期986-988,共3页Chinese Journal of Experimental Surgery
基 金:基金项目:江苏省六大人才高峰基金(2014-WSW-033)
摘 要:目的 探讨LASP-1基因在胶质瘤细胞迁移和侵袭中的作用及其机制.方法 运用Control小干扰RNA (siRNA)(Ctrl组)、LASP-1 siRNA(siRNA组)分别转染人脑胶质瘤细胞U251、U87,Western blot检测LASP-1、磷酸化黏着斑激酶(p-FAK)、Src、基质金属蛋白酶(MMP)-2和MMP-9蛋白表达量.检测沉默LASP-1基因对胶质瘤细胞黏附、迁移和侵袭能力的影响.结果 与Ctrl组比较siRNA组U87和U251细胞中LASP-1蛋白表达量降低;U87和U251黏附能力下降了59.14%和62.37%,迁移能力分别下降55.61%和56.07%,侵袭能力分别下降48.62%和56.31%.干扰LASP-1表达后siRNA组p-FAK、Src、MMP-2和MMP-9蛋白表达量较Ctrl组均明显降低,差异均有统计学意义(P<0.05).结论 干扰LASP-1基因通过p-FAK-Src信号通路,抑制MMP-2和MMP-9蛋白表达,从而抑制胶质瘤细胞的黏附、迁移和侵袭能力.Objective To investigate the effect and mechaIlism of LIM and SH3 protein 1 (LASP-1) on the adhesion,migration and invasion of human glioma cells.Methods The small interfering RNA (siRNA group) LASP-1 and Control siRNA (Ctrl group) were transfected into the U87 and U251 glioma cells using SilentFect Lipid Reagent.The expression of LASP-1 and the expression levels of phosphorylated focal adhesion kinase (p-FAK),Src,matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) proteins after LASP-1 was konckdowned in both ofglioma cell lines were assessed by Western blotting.Results Compared to the Ctrl group,the siRNA group could decrease the expression of LASP-1 in both glioma cell lines significantly.The adhesion ability of U87 and U251 treatment with siRNA decreased by 59.14% and 62.37% and the cell migration ability reduced by 55.61% and 56.07% and the invasion ability was restrained by 48.62% and 56.31%.The expression of p-FAK,Src,MMP-2,MMP-9 and LASP-1 protein in siRNA group was significantly lower than that in Ctrl group.Conclusion Silencing LASP-1 gene inhibits the expression of MMP-2 and MMP-9 proteins through the p-FAK-Src pathway,which can inhibit the adhesion,migration and invasion of glioma cells.
分 类 号:R329.25[医药卫生—人体解剖和组织胚胎学]
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