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首页|期刊导航|山东医药|lncR FOXD2-AS1调控miR-145-5p对非小细胞肺癌细胞生物学特性的影响

lncR FOXD2-AS1调控miR-145-5p对非小细胞肺癌细胞生物学特性的影响

王巍 王志武 于镓锐 董量 曹博 李剑锋

山东医药2024,Vol.64Issue(10):45-48,4.
山东医药2024,Vol.64Issue(10):45-48,4.DOI:10.3969/j.issn.1002-266X.2024.10.010

lncR FOXD2-AS1调控miR-145-5p对非小细胞肺癌细胞生物学特性的影响

Effect of lncR-FOXD2-AS1 regulating miR-145-5p on biological characteristics of non-small-cell lung cancer cells

王巍 1王志武 1于镓锐 1董量 1曹博 2李剑锋3

作者信息

  • 1. 唐山市人民医院放化二科,河北唐山 063000
  • 2. 唐山市人民医院普外科
  • 3. 唐山市人民医院胸外科
  • 折叠

摘要

Abstract

Objective To investigate the effects of long non-coding RNA(lncR)-FOXD2-AS1 regulating microRNA(miR)-145-5p on proliferation,migration,invasion,and epithelial-mesenchymal transition(EMT)in non-small-cell lung cancer(NSCLC)cells.Methods Human NSCLC cell lines A549,H1299,SK-MES-1,and human normal pulmonary bronchial epithelial cell line 16HBE were cultured in vitro.The expression of lncR-FOXD2-AS1 and miR-145-5p in each cell line was detected using RT-qPCR.SK-MES-1 cells with relatively high expression of lncR-FOXD2-AS1 were selected as the research object for knockdown experiments.SK-MES-1 cells were divided into the NC group(transfected with si-NC)and si-FOXD2-AS1 group(transfected with si-FOXD2-AS1)according to different transfection treatments.After transfection,qRT-PCR was used to detect the expression of lncR-FOXD2-AS1 and miR-145-5p in the cells,CCK-8 was used to detect cell proliferation activity,Transwell experiment was used to detect cell migration and invasion abilities,and Western blotting was used to detect the expression of E-cadherin,N-cadherin,and Fibronectin proteins in cells.The dual luciferase experiment verified the relationship between lncR-FOXD2-AS1 and miR-145-5p.Results Compared with 16HBE cells,lncR-FOXD2-AS1 was highly expressed in NSCLC cell lines(P<0.05),and miR-145-5p was low expressed in NSCLC cell lines(P<0.05).Compared with the NC group,the expression of miR-145-5p in the si-FOXD2-AS1 group increased(P<0.05),the OD values at 0,24,and 48 h decreased(all P<0.05),the number of migrating and invading transmembrane cells became smaller(P<0.05),the expression of E-cadherin protein increased(P<0.05),and the ex-pression levels of N-cadherin and Fibronectin proteins decreased(all P<0.05).The dual luciferase experiment confirmed that miR-145-5p was the target gene of lncR-FOXD2-AS1(P<0.05).Conclusions The expression of lncR-FOXD2-AS1 is elevated in NSCLC.Knocking down lncR-FOXD2-AS1 inhibits the proliferation,migration,invasion,and EMT processes of NSCLC cells by targeting miR-145-5p.

关键词

非小细胞肺癌/长链非编码RNA-FOXD2-AS1/微小RNA-145-5p/细胞增殖/细胞迁移/细胞侵袭/上皮-间质转化

Key words

non-small-cell lung cancer/long non-coding RNA-FOXD2-AS1/microRNA-145-5p/cell prolifera-tion/cell migration/cell invasion/epithelial-mesenchymal transition

分类

医药卫生

引用本文复制引用

王巍,王志武,于镓锐,董量,曹博,李剑锋..lncR FOXD2-AS1调控miR-145-5p对非小细胞肺癌细胞生物学特性的影响[J].山东医药,2024,64(10):45-48,4.

基金项目

河北省医学科学重点课题计划项目(20221809). (20221809)

山东医药

1002-266X

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