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作 者:袁杰[1] 涂刚[1] 陈茂山[1] 朱庆[1] 杨丽[2] 成宏 杨光伦[1]
机构地区:[1]重庆医科大学附属第一医院内分泌乳腺外科,重庆400016 [2]重庆医科大学临床检验诊断学教育部重点实验室,重庆400016 [3]恩施土家族苗族自治州中心医院乳腺外科,湖北445000
出 处:《重庆医科大学学报》2015年第2期247-251,共5页Journal of Chongqing Medical University
基 金:国家自然科学基金面上资助项目(编号:81072149)
摘 要:目的:构建整合素β1(integrinβ1,ITGβ1)基因干扰慢病毒载体,并研究ITGβ1对他莫昔芬耐药乳腺癌MCF-7细胞(Tamoxifen-resistant MCF-7,MCF-7R)的迁移和侵袭能力的影响。方法:针对ITGβ1靶序列设计合成4条sh RNA序列及1条阴性对照序列NC,构建ITGβ1RNAi慢病毒载体及对照病毒载体,并分别进行病毒包装,通过内源性筛靶,选取干扰效果最好的组病毒感染MCF-7R细胞,Western blot检测ITGβ1蛋白的表达水平;Transwell实验检测细胞迁移和侵袭能力。结果:成功构建4条慢病毒干扰重组质粒,并分别包装成病毒,通过内源性筛靶挑选出干扰效果最佳的慢病毒组,感染MCF-7R细胞后ITGβ1基因的蛋白表达量较NC组明显降低(P=0.000),且细胞的迁移和侵袭能力明显弱于NC组(P=0.000)。结论:慢病毒介导的sh RNA可有效地干扰MCF-7R细胞中ITGβ1的表达,并且抑制MCF-7R细胞的迁移和侵袭能力。Objective:To construct lentivirus vector targeting integrin β1(ITGβ1)gene and to study its effect on migration and invasion of Tamoxifen-resistant MCF-7(MCF-7R). Methods:Four sh RNA sequences targeting ITGβ1 gene and one negative control sequence were designed,and were cloned into lentivirus vector,respectively. Recombinant lentivirus and control were extracted after transfecting 293 T with the recombinant vector and helper vectors. The lentivirus with the best interfering effect was determined by real-time PCR and was chosen to infect MCF-7R. The expression of ITGβ1 gene was determined by Western blot. Transwell assay was used to detect the difference of migration and invasion. Results:Four recombinant lentivirus vectors were successfully constructed and the packaged lentivirus with the best interfering effect was used to infect MCF-7R. Western blot results showed that the protein expression of ITGβ1 was significantly reduced in MCF-7R(P=0.000)and its migration and invasion abilities were markedly suppressed(P=0.000).Conclusion:Lentivirus vector targeting ITGβ1 gene can efficiently suppress the expression of ITGβ1 in MCF-7R,thereby leading to decreased migration and invasiveness abilities of MCF-7R
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