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microRNA-139-5p及其靶基因Notch1在结直肠癌中的作用
引用本文:廖信芳,李正荣,杨清水,张乡城,李柱,揭志刚.microRNA-139-5p及其靶基因Notch1在结直肠癌中的作用[J].中国普通外科杂志,2014,23(10):1373-1378.
作者姓名:廖信芳  李正荣  杨清水  张乡城  李柱  揭志刚
作者单位:(1. 南方医科大学附属南海医院 普外二科,广东 佛山 528200;2. 南昌大学第一附属医院 胃肠外科,江西 南昌 330006)
摘    要:目的:探讨microRNA-139-5p(miR-139-5p)在结直肠癌中的表达及其对结直肠癌细胞转移和侵袭的影响。 方法:用荧光定量PCR方法检测miR-139-5p在结直肠癌组织与不同结直肠癌细胞株中的表达变化;用Boyden小室分析和伤口愈合实验检测miR-139-5p转染及miR-139-5p抑制对结直肠癌细胞转移和侵袭能力的影响;生物信息学方法预测miR-139-5p的靶基因,并采用荧光素酶报告基因实验验证,Western blot方法检测miR-139-5p转染对靶基因表达的影响。 结果:与各自的正常对照组比较,结直肠癌组织与结直肠癌细胞系中miR-139-5p表达均明显降低(P<0.05)。结直肠癌DLD1细胞和HCT116细胞转染miR-139-5p后,转移与侵袭能力均明显降低(均P<0.05),而miR-139-5p抑制剂处理后,两种细胞的的侵袭能力均明显增强(均P<0.05)。生物信息学预测显示,Notch1是miR-139-5p的靶基因,且得到荧光素报告实验结果证实。Western blot结果显示,转染miR-139-5p后,结直肠癌DLD1细胞和HCT116细胞中Notch1蛋白表达均明显下调(均P<0.05)。 结论:miR-139-5p可能通过调节Notch1的表达而抑制肿瘤细胞的转移和侵袭,而下调的miR-139-5p可能在结直肠癌的发生发展中起了重要作用。

关 键 词:结直肿瘤  微RNAs  miR-139-5p  Notch1
收稿时间:2014/8/14 0:00:00
修稿时间:2014/9/13 0:00:00

Role of microRNA-139-5p and its target gene Notch1 in colorectal cancer
LIAO Xinfang,LI Zhengrong,YANG Qingshui,ZHANG Xiangcheng,LI Zhu,JIE Zhigang.Role of microRNA-139-5p and its target gene Notch1 in colorectal cancer[J].Chinese Journal of General Surgery,2014,23(10):1373-1378.
Authors:LIAO Xinfang  LI Zhengrong  YANG Qingshui  ZHANG Xiangcheng  LI Zhu  JIE Zhigang
Institution:(1 The Second Department of General Surgery, Affiliated Nanhai Hospital, Southern Medical University, Guangzhou 528200, China; 2. Department of Gastrointestinal Surgery, the First Affiliated Hospital, Nanchang University, Nanchang 330006, China)
Abstract:Objective: To investigate the effect of microRNA-139-5p (miR-139-5p) expression in colorectal cancer and its influence on migration and invasion ability of colorectal cancer cells. Methods: The expression alteration of miR-139-5p in colorectal cancer tissue and different colorectal cancer cell lines were detected by using fluorescent quantitative PCR. The influence of miR-139-5p transfection or miR-139-5p inhibitor treatment on migration and invasion ability of colorectal cancer cells were detected by Boyden chamber assay and wound healing assay. The target gene of miR-139-5p was predicted by bioinformatics analysis and was identified by luciferase reporter assay, and then the influence of miR-139-5p transfection on its target gene expression was determined by Western blot analysis. Results: The miR-139-5p mRNA expressions in both colorectal cancer tissue and colorectal cancer cell lines were significantly decreased compared with corresponding control (all P<0.05). The migration and invasion ability in colorectal cancer DLD1 and HCT116 cells were significantly decreased after miR-139-5p transfection and were significantly increased after miR-139-5p inhibitor treatment (all P<0.05). Bioinformatics analysis showed that Notch1 was the potential target gene of miR-139-5p which was then identified by luciferase reporter assay. Western blot results showed that Notch1 protein expressions in DLD1 and HCT116 cells were significantly down-regulated after miR-139-5p transfection (both P<0.05). Conclusion: MiR-139-5p may inhibit the migration and invasion of cancer cells through regulating its target gene Notch1, so the down-regulated miR-139-5p may play an important role in the occurrence and development colorectal cancer.
Keywords:Colorectal Neoplasms  MicroRNAs  miR-139-5p  Notch1
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