摘要
目的:探讨蛋白磷酸酯酶2A(PP2A)在宫颈癌迁移中的作用。方法:培养Hela宫颈癌细胞,通过药物或质粒转染干预PP2A水平。药物实验中将Hela细胞分为3组,即正常对照组(DMSO处理,n=6),DES组(10nM PP2A激动剂DES处理,n=6)和OA组(10nM PP2A抑制剂OA处理,n=6);质粒转染实验中将Hela细胞分为DsRed-vector组(n=6),DsRed-PP2Ac组(n=6)和DsRed-siPP2Ac组(n=6),按分组要求转染相应质粒。采用划痕实验观察各组不同时间点(药物0h、24h、48h;转染0h、48h)Hela细胞迁移情况并比较组间差异。结果:药物或基因上调PP2A可显著抑制宫颈癌细胞的迁移,而药物或基因下调PP2A水平则明显促进宫颈癌细胞的迁移。结论:PP2A在宫颈癌的发展中起重要的作用,该研究可为宫颈癌的发展提供新的分子机制,亦可为宫颈癌临床药物的开发提供新的靶点。
Objective:To explore the role of protein phosphatase 2 A(PP2 A)in the migration of cervical cancer.Method:Hela cervical cancer cells were cultured and PP2 Alevels were intervened by drug or plasmid transfection.In the drug experiment,Hela cells were divided into three groups,namely normal control group(DMSO treatment,n=6),DES group(10 nM PP2 Aagonist DES treatment,n=6)and OA group(10 nM PP2 Ainhibitor OA treatment,n=6).Hela cells were divided into DsRed-vector group(n=6),DsRed-PP2 Ac group(n=6)and DsRed-siPP2 Ac group(n=6)in plasmid transfection experiments,and the corresponding plasmids were transfected according to grouping requirements.Scratch test was used to observe the migration of Hela cells at different time points(administration0 h,24 h,48 h;transfection 0 h,48 h)and the differences between groups were compared.Result:Upregulation of PP2 A pharmacologically and genetically could inhibit Hela cells migration,however,downregulation of PP2 Apharmacologically and genetically could promote Hela cells migration.Conclusion:PP2 Aplayed an important role in the cervical cancer development,and also would provide new molecular targets for clinical drug research.
作者
申复进
郑红云
廖淑梅
许学先
SHEN Fu-jin 1,ZHENG Hong-yun 2, ,LIAO Shu-mei 2,XU Xue-xian 1(1Department of Obstetrics and Gynecology, 2Department of Clinical Laboratory,Renmin Hospital of Wuhan University,Wuhan 430060,China; #Corresponding autho)
出处
《微循环学杂志》
2018年第3期1-5,共5页
Chinese Journal of Microcirculation
基金
国家自然科学基金(81100395)
湖北省自然科学基金(2015CFB723)