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作 者:许涛[1] 张磊[2] 杨涛[1] 曹好好[1] 熊俊[2]
机构地区:[1]华中科技大学同济医学院附属普爱医院重症医学科,湖北武汉430033 [2]华中科技大学同济医学院附属协和医院肝胆外科,湖北武汉430022
出 处:《武汉大学学报(医学版)》2015年第5期677-680,共4页Medical Journal of Wuhan University
基 金:湖北省自然科学基金项目(编号:2011CDB103)
摘 要:目的:探讨USP22基因在氟尿嘧啶对肝癌细胞毒性作用中的影响。方法:用Western blotting检测肝癌细胞HepG2和BEL7402中USP22基因的表达状态,构建并对肝癌细胞转染USP22基因的siRNA(siRNAUSP22),然后以氟尿嘧啶处理24h后,MTT检测法观察在USP22基因沉默前后,氟尿嘧啶对肝癌细胞活性的影响。结果:USP22基因在肝癌细胞中显著高表达。siRNA-USP22转染后显著抑制USP22基因的表达,同时可明显增强氟尿嘧啶对HepG2和BEL7402细胞的毒性作用,降低其细胞活性[(53.2±6.8)%,P<0.05;(49.8±7.3)%,P<0.05]结论:下调USP22基因可提高肝癌细胞对氟尿嘧啶的敏感性,提示USP22高表达可能是造成肝癌化疗抵抗的原因之一。Objective: To investigate the influence of USP22 gene in cytotoxic effect of fluorouracil on hepatocarcinoma cells. Methods: Expression status of USP22 gene was detected by Western blot- ting in HepG2 and BELT402 hepatocarcinoma cell lines, siRNA of USP22 (siRNA-USP22) was constructed and transfected in hepatocarcinoma cells for 24 h. The influence of fluorouracil to hepatocarcinoma cellular activity was assessed by MTT assay before and after USP22 silence. Results: USP22 was significantly upregulated in hepatocarcinoma cells. Transfection of siRNA- USP22 obviously inhibited expression of USP22 in hepatocarcinoma cells and enhanced the cyto- toxic effect of fluorouracil on HepG2 and BEL7402 cells. Their cellular activities decreased to (3.2±6. 8)% and (49. 8± 7. 3)V0 respectively (P〈0. 05). Conclusion: Downregulation of USP22 may enhance the sensitivity of hepatocarcinoma cells to fluorouracil, suggesting that increased expression of USP22 may be one of the reasons for hepatocarcinoma chemotherapy resistance.
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