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首页|期刊导航|中国医科大学学报|NKX2-1-AS1介导miR-96-5p/PRDM16轴对未分化甲状腺癌细胞增殖、迁移和侵袭的影响

NKX2-1-AS1介导miR-96-5p/PRDM16轴对未分化甲状腺癌细胞增殖、迁移和侵袭的影响

郭宏鹏 李尤 刘奇 张睿 孙成林 潘星合

中国医科大学学报2024,Vol.53Issue(6):547-554,8.
中国医科大学学报2024,Vol.53Issue(6):547-554,8.DOI:10.12007/j.issn.0258-4646.2024.06.011

NKX2-1-AS1介导miR-96-5p/PRDM16轴对未分化甲状腺癌细胞增殖、迁移和侵袭的影响

Effects of NKX2-1-AS1-mediated miR-96-5p/PRDM16 axis on anaplastic thyroid cancer cell proliferation,migration,and invasion

郭宏鹏 1李尤 2刘奇 3张睿 2孙成林 2潘星合2

作者信息

  • 1. 沈阳市苏家屯区中心医院普外科,沈阳 110101
  • 2. 沈阳医学院附属中心医院普外一科,沈阳 110024
  • 3. 沈阳医学院附属中心医院放射科,沈阳 110024
  • 折叠

摘要

Abstract

Objective To explore the effects of the long non-coding RNA(lncRNA)NK2 homeobox 1-antisense RNA 1(NK2-1-AS1),which mediates the microRNA(miR)-96-5p/PR domain-containing protein 16(PRDM16)axis,on anaplastic thyroid cancer(ATC)cell proliferation,migration,and invasion in vitro and transplanted tumor growth in vivo.Methods The differentially expressed lncRNA NKX2-1-AS1 in ATC tissues and cells,its target miRNA miR-96-5p,and its downstream target gene PRDM16 were screened using a bioinformatics analysis.The dual-luciferase reporter assay validated the relationship between NKX2-1-AS1 and miR-96-5p as well as the connection between miR-96-5p and PRDM16.Western blotting was performed to detect the effect of miR-96-5p overexpression on PRDM16 in CAL-62 cells overexpressed with NKX2-1-AS1.Plate clone formation,scratch,and Transwell assays were used to detect the effects of PRDM16knockdown on the proliferation,migration,and invasion of CAL-62 cells overexpressing NKX2-1-AS1.CAL-62 cells were injected subcutaneously into nude mice and the effect was observed of PRDM16knockdown on the growth of transplanted tumors of CAL-62 cells overexpressing NKX2-1-AS1.Results The bioinformatics analysis revealed that the NK2-1-AS1/miR-96-5p/PRDM16 axis was involved in regulating ATC development.The dual-luciferase reporter assay demonstrated that NKX2-1-AS1 bound to miR-96-5p and miR-96-5p bound to PRDM16.NKX2-1-AS1 overexpression upregulated PRDM16 protein expression in CAL-62 cells,while miR-96-5p overexpression reversed this phenomenon.NKX2-1-AS1 overexpression inhibited CAL-62 cellular proliferation,migration,and invasion in vitro and transplanted tumor growth in vivo,while knocking down PRDM16 reversed these phenomena.Conclusion NK2-1-AS1 may compete with miR-96-5p as an endogenous RNA to bind to its downstream target gene,PRDM16,and upregulate its expression,thus inhibiting ATC cell proliferation,migration,and invasion in vitro and transplanted tumor growth in vivo.

关键词

NKX2-1-AS1/miR-96-5p/PRDM16/未分化甲状腺癌

Key words

NKX2-1-AS1/miR-96-5p/PRDM16/anaplastic thyroid cancer

分类

医药卫生

引用本文复制引用

郭宏鹏,李尤,刘奇,张睿,孙成林,潘星合..NKX2-1-AS1介导miR-96-5p/PRDM16轴对未分化甲状腺癌细胞增殖、迁移和侵袭的影响[J].中国医科大学学报,2024,53(6):547-554,8.

基金项目

辽宁省科学技术计划重大科研项目(2022JH2/101300035) (2022JH2/101300035)

沈阳市科学技术计划(21-173-9-18) (21-173-9-18)

沈阳医学院硕士研究生科技创新基金(Y20220531) (Y20220531)

中国医科大学学报

OA北大核心CSTPCD

0258-4646

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