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微小RNA-433-3p靶向同源异形盒基因A1抑制胃癌MGC-803细胞增殖、侵袭的研究

Experimental study of miR -433 -3p targeting HOXA1 to inhibit the proliferation and invasion of gastric MGC-803 cancer cells

发布日期:2023-07-17 17:39:48 阅读次数: 0 下载


作者:赵轶峰1,李明霞2,张超3,胡晓敏1,王雄1,赵铁军1

 

单位:1.河北北方学院附属第一医院 胃肠肿瘤外科,河北  张家口 075000; 2.河北北方学院附属第一医院 内分泌与代谢病科,河北 张家口 075000; 3.河北北方学院附属第一医院 介入科,河北 张家口075000

 

Authors: Zhao Yifeng1Li Mingxia2Zhang Chao3Hu Xiaomin1Wang Xiong1Zhao Tiejun1

 

Unit: 1.Department of Gastrointestinal Tumor Surgerythe First Hospital Affiliated to Hebei North UniversityZhangjiakou 075000HebeiChina; 2.Department of Internal Medicine and Metabolic Diseasesthe First Hospital Affiliated to Hebei North UniversityZhangjiakou 075000HebeiChina; 3.Department of Interventionalthe First Hospital Affiliated to Hebei North UniversityZhangjiakou 075000HebeiChina

 

摘要:

目的 探讨微小RNA-433-3p(miR-433-3p)靶向同源异形盒基因A1 (HOXA1)对胃癌MGC-803细胞增殖、侵袭的影响。方法 体外培养人胃癌MGC-803细胞,分为对照组(正常培养,不进行任何处理)、si-NC组(转染miR-433-3p siRNA阴性对照)、si-miR-433-3p组(转染miR-433-3p siRNA)、mimic-NC组(转染miR-433-3p mimic阴性对照)和miR-433-3p mimic组(转染miR-433-3p mimic)。荧光定量聚合酶链反应(PCR)法检测MGC-803细胞中miR-433-3p及HOXA1 mRNA表达;细胞计数法、Transwell法分别检测MGC-803细胞增殖、侵袭;双荧光素酶报告基因试验检测miR-433-3p与HOXA1的靶向关系。结果 与对照组和si-NC组相比,si-miR-433-3p组MGC-803细胞中miR-433-3p表达降低(P<0.05),HOXA1 mRNA表达、细胞增殖率、侵袭细胞数升高(P<0.05)。与对照组和mimic-NC组相比,miR-433-3p mimic组MGC-803细胞中miR-433-3p表达升高(P<0.05),HOXA1 mRNA表达、细胞增殖率、侵袭细胞数降低(P<0.05)。TargetScan网站预测及双荧光素酶报告基因试验结果显示,miR-433-3p与HOXA1在MGC-803细胞中存在靶向关系。结论 miR-433-3p能靶向调控HOXA1抑制胃癌MGC-803细胞的增殖、侵袭过程。 

 

关键词:微小RNA-433-3p;同源异形盒基因A1;胃癌MGC-803 细胞;增殖;侵袭

 

Abstract

Objective To investigate the effects of microRNA-433-3p miR-433-3p targeting homeobox gene A1 HOXA1 on the proliferation and invasion of gastric cancer MGC-803 cells. Method Human gastric cancer cells MGC-803 were cultured in vitro and divided into control group si-NC groupsimiR-433 -3p groupmimic -NC groupand miR-433 -3p mimic group. Real -time fluorescent quantitative PCR method was used to detect the expression of miR-433-3p and HOXA1 mRNA in MGC-803 cells. Cell countingTranswell method were used to detect the proliferationinvasion of MGC -803 cells. The dual luciferase reporter gene experiment was used to detect the targeting relationship between miR-433 -3p and HOXA1. Result Compared with the control group and si-NC groupthe expression level of miR-433-3pin MGC-803 cells in the si-miR-433-3p group reduced P<0.05),the HOXA1 mRNA expression levelcell proliferation rate number of invasive cells increased P<0.05. Compared with the control group and mimic-NC groupthe expression level of miR-433-3p in MGC-803 cells in the miR-433-3p mimic group increased significantlyP<0.05),the HOXA1 mRNA expression levelcell proliferation ratenumber of invasive cells reduced P<0.05. TargetScan website prediction and dual luciferase reporter gene experiment results showed that miR-433-3p and HOXA1 had a targeting relationship in MGC-803 cells. Conclusion miR-433-3p can target HOXA1 to inhibit the proliferation and invasion of gastric cancer MGC-803 cells.

 

Key Words: MicroRNA-433-3p;  Homeobox gene A1;  Gastric MGC-803 cancer;  Proliferation;  Invasion

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