检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:刘峻[1,3] 严玉兰[2] 张金[2] 刘洋[2] 张杰[3] 梁冰[3] 步雪峰[1]
机构地区:[1]江苏镇江市江苏大学附属人民医院普外科,212002 [2]江苏大学附属人民医院呼吸科 [3]江苏大学临床医学院
出 处:《中华微生物学和免疫学杂志》2013年第7期507-512,共6页Chinese Journal of Microbiology and Immunology
基 金:江苏省镇江市2011社发科技支撑项目(SH2011037)
摘 要:目的探讨Ad-hIFN-λ1重组腺病毒对胃腺癌细胞SGC-7901增殖的影响及其机制。方法分别用Ad-hIFN-λ1重组腺病毒、Ad-LacZ空质粒及PBS对照组作用于人胃腺癌细胞SGC-7901,MTT法测定细胞增殖情况,RT-PCR检测胃癌SGC-7901中IFN-λ1mRNA的表达,免疫荧光法检测hIFN-λ1蛋白的表达,Tunel、流式细胞术检测细胞凋亡。结果Ad-hIFN-λ1转染胃腺癌细胞SGC-7901后,肿瘤细胞生长明显抑制,细胞中hIFN-λ1 mRNA、蛋白高效表达,细胞凋亡率明显高于Ad-LacZ组、PBS空白对照组。结论Ad-hIFN-λ1重组腺病毒转染至胃腺癌细胞SGC-7901后表达IFN-λ1,Ad-hIFN-λ1能够显著抑制人胃腺癌SGC-7901细胞生长,并可能通过诱导其凋亡而起作用。Objective To explore the effects of Ad-hIFN-λ1 recombinant adenovirus on prolifera- tion of gastric adenocareinoma cell line SGC-7901 and its mechanism. Methods Ad-hlFN-λ1 recombinant adenovirus and empty plasmid Ad-LacZ were respectively transfated to human gastric adenocarcinoma SGC- 7901 cells. The proliferation of transfected cells was detected by MTT assay. IFN-λ1l gene expression at mR- NA and protein levels in the ceils were measured by RT-PCR analysis and immunofluoreseenee assay, re- spectively. Tunel assay and flow eytometry were used to analyze the rate of cell apoptosis. Results The proliferation of gastric adenoeareinoma SGC-7901 cells were significantly inhibited with Ad-hlFN-λ1 inter- vention in accordance with highly expressed IFN-λ1at mRNA and protein levels, respectively. The apoptosis rate of Ad-hlFN-λ1 transfeeted cells was markedly higher than that of the empty plasmid Ad-LaeZ group and PBS blank control group. Conclusion The expression of hlFN-λ1 could be detected after transfection of Ad-hlFN-λ1 recombinant adenovirus into gastric adenocareinoma SGC-7901 cells. Ad-hlFN-λ1 could signifi- cantly inhibit the proliferation of gastric adenocarcinoma SGC-7901 cells by promoting the apoptosis of cancer cells.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.159