中国癌症杂志 ›› 2014, Vol. 24 ›› Issue (4): 273-278.doi: 10.3969/j.issn.1007-3969.2014.04.006

• 论著 • 上一篇    下一篇

miR-486-5p对胃癌细胞株SGC7901生物学行为的影响

李明1*,连海峰1,刘成霞1,胡营滨1,李有杰2   

  1. 1. 滨州医学院附属医院消化内科,山东 滨州 256603 ;
    2. 滨州医学院肿瘤分子生物学重点实验室,山东 烟台 264003
  • 出版日期:2014-04-30 发布日期:2014-05-06
  • 通信作者: 刘成霞 E-mail:phdlcx@163.com
  • 作者简介:*:现在滨州医学院烟台附属医院消化内科工作。
  • 基金资助:
    山东省高校科技计划(No:J11LF75);滨州医学院科研启动基金(No:BY2010KYQD02)

Relationship between miR-486-5p and biological behavior of gastric carcinoma SGC7901 cells

LI Ming1, LIAN Hai-feng1, LIU Cheng-xia1, HU Ying-bin1, LI You-jie2   

  1. 1.Department of Digestive, the Affiliated Hospital of Binzhou Medical University, Binzhou Shandong 256603, China; 2.Key Laboratory of Tumor Molecular Biology, Binzhou Medical University, Yantai Shandong 264003, China
  • Published:2014-04-30 Online:2014-05-06
  • Contact: LIU Cheng-xia E-mail: phdlcx@163.com

摘要:

背景与目的:既往研究表明微小RNA-486-5p(miR-486-5p)在多种肿瘤的进展中起重要作用,但其在胃癌中作用的研究较少,本研究旨在探讨miR-486-5p对胃癌细胞株SGC7901增殖、凋亡及迁移能力的影响。方法:使用实时定量PCR(quantification real-time PCRqRT-PCR)检测胃癌细胞株SGC7901及胃黏膜上皮细胞GES-1miR-486-5p的表达,构建miR-486-5p过表达质粒,使用脂质体法瞬时转染胃癌细胞株SGC7901qRT-PCR检测转染细胞后miR-486-5p的表达丰度,噻唑蓝(MTT)法及流式细胞仪检测细胞的增殖及凋亡情况,Transwell小室迁移实验检测细胞的迁移能力。结果:miR-486-5pSGC7901细胞中表达明显下调,SGC7901细胞转染miR-486-5p过表达质粒后,miR-486-5p表达明显上调,细胞增殖、迁移能力降低,凋亡率增高,差异均有统计学意义(P<0.05)结论:miR-486-5p可抑制胃癌细胞株SGC7901的增殖和迁移。

关键词: 胃癌, 微小RNA-486-5p, 增殖, 凋亡, 迁移

Abstract:

Background and purpose: MicroRNA-486-5p (miR-486-5p) has been demonstrated to play an important role in many kinds of tumor, however, there are few reports about the relationship between miRNA-486-5p in gastric carcinoma. This study was aimed to explore the effect of miR-486-5p on the proliferation, apoptosis and migration abilities of the human gastric cancer cell line SGC7901. Methods: Quantitative real-time PCR (qRTPCR) analysis was performed to detect the expression of miR-486-5p in the SGC7901 and GES-1 cells, miR-486-5p over-expressing plasmid was constructed and transfected into the human gastric carcinoma cell line SGC7901 using LipofectamineTM2000. The expression of miR-486-5p of the transfected cells was measured by qRT-PCR, the proliferation level of SGC7901 cells was detected by MTT method, the apoptosis rate of the cells was measured by flow cytometry and the in vitro migration abilities of SGC7901 cells by transwell test. Results: The miR-486-5p expression in SGC7901 cells was down-regulated compared with GES-1 cells. The expression of miR-486-5p in SGC7901 cells that was transfected miR-486-5p over-expressing plasmid was obviously up-regulated. The proliferation and migration abilities of SGC7901 cells were inhibited significantly, and the apoptosis rate of the cells increased. Conclusion: miR-486-5p can effectively suppress the proliferation and in vitro migration abilities of SGC7901 cells, indicating that miR-486-5p might be used as a target for molecular therapy of gastric cancer.

Key words: Gastric carcinoma, miR-486-5p, Proliferation, Apoptosis, Migration abilities