| 注册
首页|期刊导航|广东医学|miR-181d靶向CREB1对5-氟尿嘧啶治疗结肠癌细胞敏感性的影响

miR-181d靶向CREB1对5-氟尿嘧啶治疗结肠癌细胞敏感性的影响

LIU Hong NONG Fei-fei DENG Shu-ye

广东医学2025,Vol.46Issue(12):1826-1834,9.
广东医学2025,Vol.46Issue(12):1826-1834,9.DOI:10.13820/j.cnki.gdyx.20243716

miR-181d靶向CREB1对5-氟尿嘧啶治疗结肠癌细胞敏感性的影响

Effect of miR-181d targeting CREB1 on the sensitivity of colorectal cancer cells to 5-fluorouracil

LIU Hong 1NONG Fei-fei 1DENG Shu-ye1

作者信息

  • 1. Laboratory of Medical Molecular Biology,the First Affiliated Hospital of Guangxi Univer-sity of Chinese Medicine,Nanning 530023,Guxnagxi,China
  • 折叠

摘要

Abstract

Objective To identify key genes regulating colorectal cancer(CRC)sensitivity to 5-fluorouracil(5-Fu)using a CRISPR/Cas9 library and to explore the role of microRNA-181d(miR-181d)in mediating this process.Methods A genome-wide CRISPR/Cas9 knockout screening system was established in Ls174t CRC cells.Bioinformatics analysis identified miR-181 d as a key regulator of 5-Fu sensitivity.Loss-of-function(miR-181 d knockout or inhibitor)and gain-of-function(miR-181 d mimic)approaches were applied to evaluate cell viability and apoptosis following 5-Fu treatment.Dual-luciferase reporter assays and Western blotting were used to confirm cAMP re-sponsive element-binding protein 1(CREB1)as a target of miR-181 d.Protein expression levels of CREB1,JUN,and FOS were further examined.Results CRISPR/Cas9 screening showed enrichment of sgRNAs targeting miR-181 d in 5-Fu-treated cells.Suppression of miR-181 d(knockout or inhibitor)significantly promoted CRC cell survival and re-duced apoptosis upon 5-Fu exposure(P<0.05).Conversely,miR-181 d overexpression inhibited cell survival and en-hanced apoptosis(P<0.05).Dual-luciferase and Western blot analyses confirmed CREB1 as a direct target of miR-181 d.Overexpression of CREB1 promoted CRC cell survival,suppressed apoptosis,and upregulated JUN and FOS protein levels(P<0.05).In contrast,miR-181d overexpression downregulated CREB1 and suppressed JUN/FOS expression(P<0.05).Conclusion miR-181d enhances the sensitivity of CRC cells to 5-Fu by targeting and downregulating CREB1,thereby inhibiting the JUN/FOS signaling pathway,reducing cell survival,and promoting apoptosis.miR-181 d may represent a promising therapeutic strategy to improve chemotherapeutic efficacy in colorectal cancer.

关键词

miR-181d/5-氟尿嘧啶敏感性/CAMP反应元件结合蛋白1/结肠癌

Key words

miR-181d/5-fluorouracil sensitivity/CAMP responsive element binding protein 1/colorectal cancer

分类

医药卫生

引用本文复制引用

LIU Hong,NONG Fei-fei,DENG Shu-ye..miR-181d靶向CREB1对5-氟尿嘧啶治疗结肠癌细胞敏感性的影响[J].广东医学,2025,46(12):1826-1834,9.

基金项目

广西高校中青年教师科研基础能力提升项目(2022KY0280,2023KY0308) (2022KY0280,2023KY0308)

广东医学

1001-9448

访问量0
|
下载量0
段落导航相关论文