目的:为探索治疗乳腺癌新途径,研究RNA干扰(RNA interferance,RNAi)对MCF-7细胞株WT 1基因表达的抑制作用。方法:设计制备多对针对WT 1基因的小干扰RNA(small interfering RNA,siRNA),转染MCF-7细胞,采用实时定量PCR(real—time quantitative polymerase chainreaction,RQ-PCR)法测定WT1 mRNA的表达,western blot测定WT1蛋白的表达,流式细胞仪检测加入长春新碱后的MCF-7细胞凋亡率。结果:siRNA能有效抑制WT1基因的表达,但不呈剂量关系,在较低浓度可维持RNAi至少4d时间,WT1基因表达下调的MCF-7细胞凋亡率增加。结论:RNAi能有效抑制MCF-7细胞中WT1基因的表达,同时转染siRNA后细胞对长春新碱敏感。
Objective:To investigate the inhibitory effect of RNA interference (RNAi) on WT 1 gene expression in MCF-7 cell line. Methods: Several pairs of small interfering RNA (siRNA) for WT 1 gene was designed and transfected into MCF-7 cells. WT1 gene expression was assessed by real-time quantitative polymerase chain reaction (RT-PCR), and WT1 protein expression was tested by western blotting. Results: Expression of WT 1 gene can be effectively suppressed by siRNA in a concentration-independent manner. RNAi could be maintained at low concentration, for example at 10 nmol/L, for at least 4 d. Conelusions:Expression of WT1 gene can be effectively inhibited by siRNA in MCF-7 cells. Simultaneous transfection with siRNA increases the sensitivity of MCF-7 cells to vincristine.