首页 | 本学科首页   官方微博 | 高级检索  
检索        

miR-373抑制剂对乳腺癌细胞生长的影响
引用本文:肖锡岗,房林,沈雷,李华,马杰.miR-373抑制剂对乳腺癌细胞生长的影响[J].同济大学学报(医学版),2011,32(4):19-22.
作者姓名:肖锡岗  房林  沈雷  李华  马杰
作者单位:同济大学附属第十人民医院甲状腺乳腺外科,上海,200072
摘    要:目的探索miR-373抑制剂对乳腺癌细胞系MCF-7生长的影响。方法设计并合成miR-373抑制剂,通过脂质体转染至MCF-7细胞,采用荧光定量聚合酶链式反应检测转染后细胞内miR-373的表达水平,同时检测Caspase-3与Caspase-8的表达情况,并应用MTT实验检测miR-373抑制剂对MCF-7细胞生长的影响。结果 miR-373抑制剂能有效抑制MCF-7细胞中miR-373的表达。转染后,MCF-7细胞中Caspase-3与Caspase-8的mRNA水平均升高(P〈0.05)。miR-373抑制剂对MCF-7细胞的生长有明显的抑制作用,抑制率随浓度升高而增加(P〈0.05)。结论 miR-373抑制物可有效抑制MCF-7细胞增殖,有望成为治疗乳腺癌的新靶点。

关 键 词:乳腺肿瘤  微小RNA  抑制剂  细胞增殖

Effects of miR-373 inhibitor on growth of breast cancer cells
XIAO Xi-gang,FANG Lin,SHEN Lei,LI Hua and MA Jie.Effects of miR-373 inhibitor on growth of breast cancer cells[J].Journal of Tongji University(Medical Science),2011,32(4):19-22.
Authors:XIAO Xi-gang  FANG Lin  SHEN Lei  LI Hua and MA Jie
Institution:(Dept.of Thyroid and Breast Surgery,Tenth People’s Hospital,Tongji University,Shanghai 200072,China)
Abstract:Objective To investigate the effects of miR-373 inhibitor on growth of breast cancer cell line MCF-7.Methods The miR-373 inhibitor was designed,synthesized and transfected into MCF-7 cells.The expression of miR-373,Caspase-3 and Caspase-8 were detected by quantitative real-time polymerase chain reaction.The cell proliferation was analyzed through MTT assay.Results miR-373 inhibitor inhibited the expression of miR-373 efficiently.The expression of Caspase-3 and Caspase-8 were up-regulated after MCF-7 cells were transfected with miR-373 inhibitor(P < 0.05 ).miR-373 inhibitor inhibited proliferation of MCF-7 cells significantly and the inhibition rate increased with the concentration of miR-373 inhibitor.Conclusion The miR-373 inhibitor can efficiently inhibit the proliferation of breast cancer MCF-7 cells,which may provide a new strategy for the target therapy of breast cancer.
Keywords:breast cancer  microRNA  inhibitor  cell proliferation
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《同济大学学报(医学版)》浏览原始摘要信息
点击此处可从《同济大学学报(医学版)》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号