作者: Guang-wen Cao , Xian-hua Gao , Yi-fang Han , Zhi-qi Yu , Chuan-gang Fu
DOI: 10.3760/CMA.J.ISSN.1671-0274.2012.01.022
关键词:
摘要: Objective To investigate the effect of multidrug resistance-associated protein 4 (MRP4) expression on radiosensitivity colorectal carcinoma cell lines in vitro.Methods The vector shRNA for RNA interference was constructed and then transfected into HCT116 line to steadily down-regulate MRP4.HCT116 cells were divided 3 groups including CON group (non-transfected),NC (negative control virus added),and KD (RNAi target added transfection).To test effectiveness interference,real-time polymerase chain reaction Western blot used measure pattern MRP4 at both mRNA levels,respectively.For examination radiosensitivity,flow cytometry calculate rate apoptotic 24 h after Gy radiation.Proliferation measured via MTT assay different time points.Results ShRNA plasmid successfully constructed.Transfection this caused steady silencing (HCT116-KD).MRP4 significantly down-regulated following (P<0.05).Twenty-four hours radiation,the apoptosis (71.7±0.8)%,significantly higher than that [ (56.1±0.9)%]and NC [(59.8±0.8)% ] (P<0.05).Fourty-eight 72 proliferation inhibited compared (P<0.05).Conclusions Expression is closely related radiotolerance carcinoma.Downregulation by enhances vitro.MRP4 may be an effective molecular marker predicting carcinoma. Key words: Colorectal carcinoma; Multidrug 4; ; Radiosensitivity