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miR-27a-3p在肺腺癌中的表达及其生物学功能

牛静静 张文桃 畅靖嘉 张昕彤 朱剑军

肿瘤预防与治疗2024,Vol.37Issue(8):641-648,8.
肿瘤预防与治疗2024,Vol.37Issue(8):641-648,8.DOI:10.3969/j.issn.1674-0904.2024.08.002

miR-27a-3p在肺腺癌中的表达及其生物学功能

Expression and Biological Functions of miR-27a-3p in Lung Adenocarcino-ma

牛静静 1张文桃 2畅靖嘉 2张昕彤 2朱剑军2

作者信息

  • 1. 710061 西安,西安市胸科医院病理科
  • 2. 030001 太原,山西医科大学基础医学院
  • 折叠

摘要

Abstract

Objective:The aim of this study was to detect the expression level of miR-27a-3p in lung adenocarcinoma(LUAD),and study the effect of miR-27a-3p on the malignant growth and migration of LUAD cells.Methods:The expres-sion level and prognostic value of miR-27a-3p in LUAD were analyzed by integrating public datasets.Inhibitor was transfect-ed to decrease the level of miR-27a-3p in LUAD cells.Cell proliferation activity was detected by EdU,cell migration was de-tected by Transwell chamber,and the level of miR-27a-3p and its targeted gene were detected by real-time fluorescent quan-titative PCR.Results:The expression of miR-27a-3p was significantly high in LUAD(P<0.05),and the expression level of miR-27a-3p was increased in cancer tissue of young LUAD patients compared with other age groups.The prognosis of LUAD patients with high expression of miR-27a-3p was poor.miR-27a-3p inhibitors remarkably attenuated cell proliferation activity and cell migration ability in LUAD(all P<0.05).Combined with public data and cell experiments,our results showed that RELN,NCALD,FZD4 and GATA2 might be downstream target genes of miR-27a-3p in LU AD.In addition,the expressions of RELN,NCALD,FZD4 and GATA2 were significantly low in LUAD(all P<0.05).Conclusion:High expres-sion of miR-27a-3p promotes the malignant growth and metastasis of LUAD cells through targeting RELN,NCALD,FZD4 and GATA2.

关键词

miR-27a-3p/肺腺癌/细胞迁移/细胞增殖

Key words

miR-27a-3p/Lung adenocarcinoma/Cell migration/Cell proliferation

分类

生物科学

引用本文复制引用

牛静静,张文桃,畅靖嘉,张昕彤,朱剑军..miR-27a-3p在肺腺癌中的表达及其生物学功能[J].肿瘤预防与治疗,2024,37(8):641-648,8.

基金项目

中国博士后科学基金(编号:2023M732157) (编号:2023M732157)

山西省基础研究计划项目(编号:202303021211114) (编号:202303021211114)

山西医科大学校级博士启动基金(编号:XD1808) This study was supported grants from China Postdoctoral Science Foundation(No.2023M732157),Science and Technology Department of Shanxi Province(No.202303021211114),and Shanxi Medical University(No.XD1808). (编号:XD1808)

肿瘤预防与治疗

OACSTPCD

1674-0904

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