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MicroRNA-129-2靶向调控SOX4抑制食管癌细胞增殖与侵袭转移的研究
引用本文:肖晶鑑,岳海英,韦婷婷,周平婷,康敏,王仁生.MicroRNA-129-2靶向调控SOX4抑制食管癌细胞增殖与侵袭转移的研究[J].安徽医学,2015,36(12):1442-1446.
作者姓名:肖晶鑑  岳海英  韦婷婷  周平婷  康敏  王仁生
作者单位:530021,南宁 广西医科大学第一附属医院肿瘤放疗科
基金项目:国家自然科学基金,广西壮族自治区科技厅青年基金,广西医科大学青年基金
摘    要:目的探讨 MicroRNA-129-2(miR-129-2)在体内外抑制食管癌细胞增殖和侵袭转移的作用及可能机制,为食管癌的预后评估及靶向治疗提供新的思路。方法将 miR-129-2 mimics 及 miR-129-2 mimics NC 基因序列分别转染到食管癌 NMC109细胞中,并设为 miR-129-2 mimics 高表达组和 miR-129-2 mimics 阴性对照组(miR-129-2 mimics NC 组),将非转染的 NMC109细胞设为空白对照组。体外实验:运用 MTT 法检测3组细胞的增殖能力、Transwell 法检测细胞侵袭能力、蛋白印迹法检测 SOX4蛋白表达。采用裸鼠体内移植瘤形成实验检测3组细胞在体内环境下的增殖能力。结果 miR-129-2 mimics 组的食管癌细胞增殖活性及侵袭能力较 miR-129-2 mimics NC 组及空白对照组明显减弱(P <0.001),而空白对照组与 miR-129-2 mimics NC 组食管癌细胞增殖性及侵袭性无明显差异(P >0.05);miR-129-2 mimics 组的食管癌细胞中,SOX4的表达下调(P <0.001);miR-129-2 mimics 组裸鼠移植瘤体积及重量明显减小(P <0.001),而 miR-129-2mimics NC 组及空白对照组无明显差异(P >0.05)。结论 miR-129-2具有抑制食管癌细胞 NMC109增殖和侵袭转移的作用,其作用机制可能与靶向下调 SOX4基因表达有关。

关 键 词:miR-129-2  SOX4  食管癌  增殖  侵袭
收稿时间:2015/11/5 0:00:00
修稿时间:2015/11/28 0:00:00

miR-129-2 inhibits proliferation and invasion of esophageal carcinoma cells by targeting of SOX4
Xiao Jingjian,Yue Haiying,Wei Tingting.miR-129-2 inhibits proliferation and invasion of esophageal carcinoma cells by targeting of SOX4[J].Anhui Medical Journal,2015,36(12):1442-1446.
Authors:Xiao Jingjian  Yue Haiying  Wei Tingting
Institution:Department of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China,Department of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China,Department of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China,Department of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China,Department of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China and Department of Radiotherapy, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China
Abstract:Objective To explore the effect of MicroRNA-129-2(miR-129-2)in suppressing the proliferation and invasion of esoph-ageal carcinoma cells in vivo and in vitro and the possible mechanism,so as to provide new thoughts for the prognosis evaluation and targeted therapy of the disease. Methods Two groups of stable-transfected cells including miR-129-2 mimics group and miR-129-2mimics NC group. A blank control group were constructed. Detecting the proliferation and invasion of the three groups of cells by MTT Assays and invasion assay in vitro,SOX4 protein expression was detected in each group of cells using Western blot method,xenograft experiments in vivo were used in investigating the effect and mechanism of miR-129-2 in proliferation and invasion of esophageal carcinoma cells. Results The esophageal carcinoma cells’proliferation and invasion activity decreased significantly after transfected MicroRNA-129-2 mimics(P < 0. 001). The esoph-ageal carcinoma cells transfected MicroRNA-129-2 mimics exhibited down expression of SOX4(P < 0. 001). Xenograft experiments showed that miR-129-2 led a significant decrease in tumor volume and weight(P < 0. 001),whereas the miR-129-2 mimics NC and blank control group indicated no effect(P > 0. 05). Conclusion miR-129-2 may suppress the proliferation,invasion and metastasis of NMC109 esophagus carcinoma cells by targeting down-regulation of SOX4 expression.
Keywords:MicroRNA-129-2  SOX4  Esophageal carcinoma  Proliferation  Invasion
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