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机构地区:[1]江苏大学附属医院消化内科,江苏省镇江市212001
出 处:《医学理论与实践》2017年第8期1100-1101,共2页The Journal of Medical Theory and Practice
摘 要:目的:研究利用重组杆状病毒介导的DNMT1siRNA对人胰腺癌细胞增殖的影响。方法:培养人胰腺癌细胞并分组如下:空白对照组、阴性对照组、病毒r-Bac-si-DNMT1-D1组(D1组)、r-Bac-si-DNMT1-D2组(D2组)、r-Bac-siDNMT1-D3组(D3组)。空白对照组仅加10%胎牛血清和DMEM培养基培养,阴性对照组、D1组、D2组、D3组加血清和DMEM培养基培养24h后依次加入空白载体r-Bac-CMV-EGFP和r-Bac-si-DNMT1-D1病毒、r-Bac-si-DNMT1-D2病毒、r-Bac-si-DNMT1-D3病毒150μl/孔,72h后分别收集各组细胞用MTT法测肿瘤细胞增殖的变化。结果:重组杆状病毒介导的DNMT1siRNA感染的细胞存活率较空白对照组和阴性对照组明显降低(P<0.05)。结论:杆状病毒介导的DNMT1siRNA感染人胰腺癌细胞后能通过降低细胞存活率,从而影响胰腺癌细胞的增殖。Objective:This study is to observe the effects of DNMT1 siRNA recombinant baculovirus on pancreatic cancer cell. Methods:Cultured Human pancreatic cancer cell and divided into five groups: control group, negative control group, r-Bac-si-DNMT1-D1 group (D1 group), r-Bac-si-DNMT1-D2 group (D2 group), r-Bac-si-DNMT1-D3 group (D3 group). Control group were cultured only with 10% FBS and DMEM. At 24h after plating with FBS and DMEM, Negative control group, D1 group, D2 group,D3 group were transfected with corresponding baculovirus-mediated RNA interference of DNMTl(150μl/well). And after 72h transfection, use MTT to test the change of cell proliferation. Results: The cell survival rate of DNMT1 siRNA recombinant baculovirus group were significant lower than that in control group and negative control group (P^0. 05). Conclusion: DNMTI siRNA recombinant baculovirus could deduce proliferation on human pancreatic cancer by lower the cell survival rate.
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