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作 者:高刚[1] 杨英杰[1] 刘建香[1] 田梅[1] 苏旭[1]
机构地区:[1]中国疾病预防控制中心辐射防护与核安全医学所,辐射防护与核应急中国疾病预防控制中心重点实验室,北京100088
出 处:《癌变.畸变.突变》2013年第2期83-86,共4页Carcinogenesis,Teratogenesis & Mutagenesis
基 金:卫生行业科研专项(201002009)
摘 要:目的:探讨过表达miR-200家族对α粒子诱发恶性转化人支气管上皮细胞(RHT35细胞)迁移能力的影响。方法:用SiPORT转染试剂转染100n mol/LmiR-200b mimic和miR-141 mimic或阴性对照(mimic control)于RHT35细胞中72h后,分别采用免疫印迹、实时荧光定量PCR技术检测过表达miR-200b和miR-141对RHT35细胞ZEB家族(ZEB1和ZEB2)及上皮间质转变相关标志分子表达的影响;并用伤口愈合实验研究过表达miR-200b和miR-141对RHT35细胞迁移能力的影响。结果:ZEB1和ZEB2蛋白在RHT35细胞中高表达。与阴性对照转染组相比,miR-200b mimic和miR-141 mimic转染组中miR-200靶基因ZEB家族表达显著下调(P<0.01);而上皮间质转变相关标志分子E-cad mRNA表达显著上调(P<0.05或P<0.01),N-cad表达显著下调(P<0.01)。与阴性对照转染组相比,miR-200b mimic和miR-141mimic转染组能显著抑制RHT35细胞的迁移能力。结论:过表达miR-200b和miR-141对RHT35细胞的迁移能力有显著抑制作用。OBJECTIVE: To explore effects of miR-200 family overexpression on migration of malignantly transformed human bronchial epithelial cells (RHT35) induced by α-particles. METHODS:The mRNA and protein levels of ZEB family (ZEB1 and ZEB2) and epithelial-mesenchymal transition marker in RHT35 was measured by Real Time PCR and western blot 72 h after transfection of 100 nmol/L miR-200b mimic, miR-141 mimic or mimic control into RHT35 cells with SiPORT reagent. In vitro wound healing assay was used to investigate whether overexpression of miR-200b and miR-141 could block migration of malignantly transformed cells induced by α-particles. RESULTS:The protein levels of ZEB1 and ZEB2 in RHT35 cells were upregulated compared with R15H20 and BEP2D cells. Overexpression of miR-200b and miR-141 led to reduced expression of ZEB1 and ZEB2 in RHT35 cells compared with mimic control (P0.01). Overexpressions of miR-200b and miR-141 upregulated E-cad expression (P0.05 or P0.01) and downregulated N-cad expression in RHT35 cells (P0.01). Overexpressions of miR-200b and miR-141 markedly blocked migration of RHT35 cells compared with mimic control. CONCLUSION:Overexpressions of miR-200b and miR-141 strongly block migration of RHT35 cells.
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