miR-34a对口腔癌细胞增殖和侵袭的影响  被引量:1

Effects of miRNA-34a on the proliferation and invasion of oral cancer cells

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作  者:单连启 黎婷[2] 蔡文燕[2] 肖丽婷[2] 孙晋虎[2] 

机构地区:[1]枣庄峄城人民医院口腔科,山东枣庄277300 [2]徐州医学院口腔医学院、徐州医学院附属医院口腔科,江苏徐州221000

出  处:《徐州医学院学报》2015年第12期912-916,共5页Acta Academiae Medicinae Xuzhou

基  金:国家自然科学基金(31060167,81160242);江苏省高校“青蓝工程”项目资助;徐州医学院优秀人才科研基金资助

摘  要:目的:观察慢病毒表达载体介导微小核糖核酸-34a( miR-34a)体外转染口腔癌细胞后对细胞增殖及侵袭的影响,探讨miRNA-34a在口腔癌发展中可能的作用。方法运用实时荧光定量PCR( RT-PCR)检测口腔癌组织、正常组织样本和口腔癌细胞系中的miR-34aRNA的表达情况,体外培养口腔癌细胞,分别对miR-34a重组慢病毒组和空白对照病毒组转染Tca8113和SCC-25细胞。采用甲基噻唑基四唑( MTT)法、克隆形成实验法检测转染目的基因细胞增殖活性的变化;采用流式细胞仪检测过表达外源性miR-34a后细胞周期分布的变化情况;采用Transwell小室实验分析转染后Tca8113和SCC-25细胞侵袭和迁移能力的改变。结果与正常组织相比,口腔癌组织中miR-34a的表达显著下调,MTT法和克隆形成率分析显示转染miR-34a基因重组慢病毒转染组与空载体慢病毒转染组比较,细胞增殖明显受到明显抑制( P<0.05);转染后细胞周期结果显示miR-34a对细胞的生长抑制作用部分是通过诱导细胞在G1期出现停滞而实现的。 Transwell小室显示与空载体慢病毒转染组相比,转染miR-34a基因重组慢病毒转染组细胞的迁移力和侵袭力也明显受到抑制(P<0.05)。结论口腔癌细胞过表达外源性miR-34a后,细胞增殖和侵袭能力明显降低,miR-34a有望在口腔癌治疗中成为新的靶点。Objective To investigate the transfection of miRNA-34a mediated by lentiviral vectors and its effects on the proliferation and invasion of oral cancer cells, as well as the role of miRNA-34a in the development of oral canc-er.Methods The expression of miRNA-34a was measured in oral cancer cell lines, oral cancer tissues and normal tis-sues by quantitative real-time PCR.Then, oral cancer Tca8113 and SCC-25 cells were transfected with miR-34a or blank control, respectively.The proliferation of these cells was measured by MTT assay and the clony formation assay. The cell cycle was determined by flow cytometry ( FCM) .The metastasis of these cells was detected by Transwell assay. Results Compared with normal tissues, the expression of miRNA-34a were down regulated in oral cancer tissues.Ac-cording to MTT assay and clony formation assay, Tca8113 and SCC-25 cells transfected with LV-miR-34a showed significantly reduced proliferation than the control (P〈0.05).Such inhibitory effects could be partly attributed to miR-34a induced cell cycle arrest at phase G1 .Moreover, miR-34a over-expression could also remarkably blocked the me-tastasis of oral cancer cells in comparison with the control (P〈0.05).Conclusions Over expression of miRNA-34a can decrease the proliferation and invasion of oral cancer cells, indicating the potential target of miRNA-34a in the treatment of oral cancer.

关 键 词:口腔癌 细胞增殖 细胞侵袭 微小核糖核酸-34a 

分 类 号:R739.8[医药卫生—肿瘤]

 

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