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作 者:董莉丽 冯磊[1] 杨然[1] 李松[1] 饶玉梅[2] DONG Li-li;FENG Lei;YANG Ran;LI Song;RAO Yu-mei(Department of Gynecology, Nanyang Central Hospital, Nanyang 473000;Department of Gynecology, the First Affiliated Hospital, Zhengzhou University, Zhengzhou 450000, China)
机构地区:[1]南阳市中心医院妇科,河南南阳473000 [2]郑州大学第一附属医院妇科,河南郑州450000
出 处:《基础医学与临床》2021年第10期1434-1439,共6页Basic and Clinical Medicine
基 金:河南省高等学校重点科研项目(18A310031)。
摘 要:目的探究内质网蛋白29(ERP29)过表达对人卵巢癌细胞系OVCAR3的侵袭、迁移能力的影响及机制。方法取对数增殖期OVCAR3细胞系,分为过表达组、空载组及对照组。过表达组用脂质体转染法转染ERP29过表达RNA重组真核载体pcDNA3.1-ERP29质粒,空载组转染阴性对照载体pcDNA3.1质粒,对照组不做处理。倒置荧光显微镜观察转染效率;用RT-qPCR检测ERP29 mRNA表达量;用Transwell小室法检测侵袭;用划痕实验检测迁移;用Western blot检测蛋白激酶B(AKT)、p-AKT、雷帕霉素靶蛋白(mTOR)、p-mTOR、真核生物始动因子4E结合蛋白1(4EBP1)、p-4EBP1蛋白表达量。结果过表达组和空载体组质粒转染效率均超过80%;与对照组和空载组相比,过表达组ERP29 mRNA相对表达量升高(P<0.05),穿膜细胞数减少(P<0.05),迁移率降低(P<0.05),p-AKT/AKT、p-mTOR/mTOR、p-4EBP1/4EBP1值均降低(P<0.05)。结论ERP29过表达可显著抑制卵巢癌细胞系OVCAR3的侵袭、迁移能力。这可能是通过下调AKT、mTOR、4EBP1磷酸化发挥作用。Objective To explore the effect of over-expression of endoplasmic reticulum protein 29(ERP29)on the invasion and migration of human ovarian cancer OVCAR3 cells,and potentially related mechanisms.MethodsThe OVCAR3 cell line at logarithmic proliferation stage was divided into over-expression group,empty vector group and control group.The over-expression group was transfected with ERP29 over-expression RNA recombinant eukaryotic vector pcDNA3.1-ERP29 plasmid by liposome transfection method.The empty vector group was transfected with the negative control vector pcDNA3.1 empty plasmid without any treatment.The transfection efficiency was examined by inverted fluorescence microscopy,The expression of ERP29 mRNA after transfection was measured by RT-qPCR.Transwell chamber experiment was used to detect the invasion.The scratch experiment was used to detect the migration.Western blot was used to detect the expression of AKT,p-AKT,mTOR,p-mTOR,4EBP1,p-4EBP1 protein.Results The plasmid transfection efficiency in over-expression group and empty vector group all exceeded 80%.Compared with the control group and the empty vector group,the relative expression of ERP29 mRNA in the over-expression group was increased(P<0.05),the number of transmembrane cells,migration rate and p-AKT/AKT,p-mTOR/mTOR,p-4EBP1/4EBP1 were all decreased(P<0.05).Conclusions Over-expression of ERP29 can significantly inhibit the invasion and migration of ovarian cancer OVCAR3 cells,the underline mechanism is potentially the inhibition by down-regulating phosphorylation of AKT,mTOR,and 4EBP1.
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