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作 者:朱玉萍[1] 李德川[1] 冯海洋[1] 刘勇[1] 钱俊[1] 陈寅波[1] 高赟[1]
机构地区:[1]浙江省肿瘤医院结直肠肿瘤外科,杭州310022
出 处:《中华胃肠外科杂志》2012年第3期292-294,共3页Chinese Journal of Gastrointestinal Surgery
基 金:浙江省自然科学基金(Y2080634)
摘 要:目的研究腺病毒介导的Bcl—XL shRNA对结肠癌细胞株的体外抗肿瘤性。方法将已有的Bcl-XL腺病毒进行扩增纯化.并通过反转录反应分析该腺病毒在mRNA水平对Bcl-XL的表达调控。通过MTT检测及克隆形成实验,了解该腺病毒对结直肠癌细胞株(Lovo细胞株)的体外杀伤作用。结果Ad/Bcl.XLshRNA作用于Lovo细胞株导致Bcl—XL mRNA表达水平下降。与对照腺病毒Ad/GFP相比,Ad/Bcl-XL shRNA显著抑制Lovo细胞的增长(P〈0.05),且该抑制效应呈剂量和时间依赖性;显著抑制Lovo细胞的克隆形成(P〈0.05),且该抑制效应呈剂量依赖性。而Ad/Bcl—XL shRNA对正常人成纤维细胞(NHFB)无明显杀伤作用。结论腺病毒介导的Bcl-XL shRNA对Lovo细胞株具有杀伤作用,可能存在潜在的结肠癌治疗价值。Objective To investigate the anti-tumor effect of adenovirus-mediated Bcl-XL shRNA on colon cancer cells in vitro. Methods A recombinant Bcl-xl adenovirus was constructed, applified, and purified. The effect on mRNA expression of Bcl-XL was assessed by RT-PCR, and the effect on apoptosis-induction of colon cancer (Lovo cell line) in vitro was assessed by MTF assay and cell clonogenic assay. Results RT-PCR showed that Ad/Bcl-XL shRNA significantly down-regulated the mRNA expression of Bcl-XL in Lovo cells. Ad/Bcl-XL shRNA suppressed the proliferation of Lovo cells in a dose-dependent as well as a time-dependent manner compared with Ad/GFP(P〈0.05). Treatment with Ad/Bcl-XL shRNA dramatically suppressed the colony formation of Lovo cells in a dose- dependent manner (P〈0.05). Ad/Bel-XL shRNA showed no effect on normal human fibroblast. Conclusion Ad/Bcl-XL shRNA exhibits cytotoxic effect on Lovo cells and may have the potential value in the treatment of colon cancer.
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