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作 者:苏允伟 祝兴旺[1] 杨玉彬[1] 刘锁民[1] 薛东炜[1] 刘屹立[1]
机构地区:[1]中国医科大学附属第四医院泌尿外科,辽宁沈阳110032
出 处:《解剖科学进展》2017年第1期54-56,60,共4页Progress of Anatomical Sciences
基 金:辽宁省科学计划项目(2015225009)
摘 要:目的探讨miR-205对膀胱癌T24细胞增殖的影响。方法合成miR-205的模拟物并转染膀胱癌T24细胞,荧光显微镜下观察转染效率,实时荧光定量PCR法检测转染48 h后,T24细胞中miR-205的表达情况,MTT法检测转染24、48和72 h后,T24细胞的增殖情况,实时荧光定量PCR法和western blot检测转染48 h后膀胱癌细胞内源性YES1 mRNA及蛋白的表达变化。结果 miR-205的模拟物转染至T24细胞的效率为80%,转染miR-205模拟物48 h后,T24细胞内miR-205的表达水平显著升高(P<0.05),T24细胞的增殖率显著低于阴性对照组(P<0.05),且呈时间依赖性,YES1 mRNA及蛋白的表达水平明显低于阴性对照组(P<0.05)。结论 miR-205抑制膀胱癌T24细胞增殖可能与靶向YES1基因相关。Objective To investigate the effect of miR-205 on the proliferation of human bladder cancer cells by directly repressing YES1. Methods miR-205 mimics and miR-205 mimics negative control were synthesized and transfected into bladder cancer T24 cells, the transfection efficiency was observed under a fluorescence microscope. The expression level of miR-205 in T24 cells w.as detected by real-time PCR at 48 h after transfection, the proliferation of T24 cells was detected by MTT assay. The expression of YES1 mRNA and protein in T24 cells was detected by real-time PCR and Western blot methods respectively after miR-205 mimics was transfected. Results The efficiency of miR-205 mimics transfection into T24 cells was 80%. Compared with negative control group, the expression level of miR-205 in T24 cells was higher after transfection with miR-205 mimics ( P〈0.05 ) , the proliferative rates of T24 cells were lower after transfeetion with miR-205 mimics (P〈0.05) with a timedependent manner. The expression levels of YES1 mRNA and protein in T24 cells were lower in transfection miR-205 mimics group than in the negative control group (P〈0.05) . Conclusion The inhibition of MiR-205 on the proliferation of T24 cells might be related to repressing YES1 gene.
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