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首页|期刊导航|局解手术学杂志|lncRNA MIR4435-2HG靶向miR-376a-3p调控胆管癌细胞生物学行为的机制研究

lncRNA MIR4435-2HG靶向miR-376a-3p调控胆管癌细胞生物学行为的机制研究

刘文东 张嘉麟 余紫丹

局解手术学杂志2024,Vol.33Issue(1):30-35,6.
局解手术学杂志2024,Vol.33Issue(1):30-35,6.DOI:10.11659/jjssx.12E022138

lncRNA MIR4435-2HG靶向miR-376a-3p调控胆管癌细胞生物学行为的机制研究

Mechanism of lncRNA MIR4435-2HG targeting miR-376a-3p to regulate the biological behavior of cholangio-carcinoma cells

刘文东 1张嘉麟 1余紫丹2

作者信息

  • 1. 惠州市第三人民医院肿瘤科,广东 惠州 516001
  • 2. 惠州市第三人民医院康复中心,广东 惠州 516001
  • 折叠

摘要

Abstract

Objective To explore the effects of long non-coding RNA(lncRNA)MIR4435-2HG(MIR4435-2HG)on the proliferation,migration,invasion and apoptosis of cholangiocarcinoma cells and its regulatory effect on microRNA-376a-3p(miR-376a-3p).Methods qRT-PCR method was used to detect the expression of MIR4435-2HG and miR-376a-3p in human intrahepatic bile duct epithelial cells HIBEpic and human cholangiocarcinoma cells RBE.si-NC,si-MIR4435-2HG,miR-NC,miR-376a-3p mimics,si-MIR4435-2HG and anti-miR-NC,and si-MIR4435-2HG and anti-miR-376a-3p were transfected into RBE cells,respectively,as the si-NC group,the si-MIR4435-2HG group,the miR-NC group,the miR-376a-3p group,the si-MIR4435-2HG+anti-miR-NC group,the si-MIR4435-2HG+ anti-miR-376a-3p group.MTT method,Transwell chamber method and flow cytometry were used to detect cell proliferation,migration,invasion and apoptosis;dual luciferase reporter gene assay was used to verify the targeting relationship between MIR4435-2HG and miR-376a-3p.Western blot was used to detect the expression of related proteins.Results The expression of MIR4435-2HG was increased in RBE cells,while the expression of miR-376a-3p was decreased(P<0.05).Compared with the si-NC group,the MIR4435-2HG expression,cell viability,and protein levels of CyclinD1,MMP-2,MMP-9 in the si-MIR4435-2HG group were reduced(P<0.05),the numbers of migrating and invading cells were reduced(P<0.05),while the MIR4435-2HG expression and apoptosis rate were increased(P<0.05).Compared with the miR-NC group,the cell viability and protein levels of CyclinD1,MMP-2,MMP-9 in the miR-376a-3p group were decreased(P<0.05),the numbers of migrating and invading cells were decreased(P<0.05),while the MIR4435-2HG expression and apoptosis rate were increased(P<0.05).MIR4435-2HG was of targeted regulation on miR-376a-3p.Compared with the si-MIR4435-2HG+ anti-miR-NC group,the cell viability and protein levels of CyclinD1,MMP-2,MMP-9 in the si-MIR4435-2HG+anti-miR-376a-3p group were increased(P<0.05),the numbers of migrating and invading cells were increased(P<0.05),while the MIR4435-2HG expression and apoptosis rate were decreased(P<0.05).Conclusion Knockdown of MIR4435-2HG can inhibit the proliferation,migration,invasion and induce apoptosis of RBE cells by targeting miR-376a-3p.

关键词

lncRNA MIR4435-2HG/miR-376a-3p/胆管癌/细胞增殖/迁移/侵袭

Key words

lncRNA MIR4435-2HG/miR-376a-3p/cholangiocarcinoma/cell proliferation/migration/invasion

分类

医药卫生

引用本文复制引用

刘文东,张嘉麟,余紫丹..lncRNA MIR4435-2HG靶向miR-376a-3p调控胆管癌细胞生物学行为的机制研究[J].局解手术学杂志,2024,33(1):30-35,6.

基金项目

惠州市医疗卫生类科技计划项目(20190401) (20190401)

局解手术学杂志

OACSTPCD

1672-5042

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