circFOXP1靶向miR-4429调控鼻咽癌6-10B细胞的增殖、迁移及侵袭OA
circFOXP1 Targets miR-4429 to Regulate Proliferation,Migration and Invasion of Nasopharyngeal Carcinoma 6-10B Cells
目的 探讨环状RNA叉头框蛋白P1(circular RNA forkhead box protein P1,circFOXP1)是否通过靶向miR-4429调控鼻咽癌6-10B细胞的增殖、迁移及侵袭.方法 分析circFOXP1和miR-4429表达与鼻咽癌患者病理特征的关系.在鼻咽癌6-10B细胞中分别转染si-NC、si-circFOXP1、pcDNA、pcDNA-circFOXP1、miR-NC、miR-4429模拟物,或同时转染si-circFOXP1与anti-miR-NC、anti-miR-4429.应用实时定量聚合酶链反应(qRT-PCR)检测鼻咽癌组织中circFOXP1和miR-4429的表达水平;采用细胞计数试剂盒8(CCK-8)、克隆形成实验、划痕实验及Transwell实验分别评估细胞活力、克隆形成能力、迁移能力及侵袭能力;Western blot法检测上皮型钙黏蛋白(E-cadherin)和神经型钙黏蛋白(N-cadherin)的表达;双萤光素酶报告基因实验验证circFOXP1与miR-4429的靶向关系.结果 鼻咽癌组织中circFOXP1的表达水平(4.61±0.31)较癌旁组织(1.00±0.05)升高(P<0.001),miR-4429的表达水平(0.37±0.03)较癌旁组织(1.00±0.08)降低(P<0.001).circFOXP1表达与TNM分期相关(P<0.05),与肿瘤体积无显著相关性(P>0.05);miR-4429表达与肿瘤体积和TNM分期均相关(P<0.05).抑制circFOXP1表达或过表达miR-4429均可降低鼻咽癌6-10B细胞的活力、克隆形成数、划痕愈合率、侵袭细胞数及N-cadherin蛋白表达,同时升高E-cadherin蛋白表达(P<0.05).circFOXP1可靶向并负向调控miR-4429的表达.干扰miR-4429能够逆转circFOXP1沉默对鼻咽癌细胞增殖、迁移及侵袭的抑制作用(P<0.05).结论 抑制circFOXP1表达可通过靶向miR-4429减弱鼻咽癌6-10B细胞的增殖、迁移及侵袭能力.
Objective To determine whether circular RNA forkhead box protein P1(circFOXP1)regulates the proliferation,migration and invasion of nasopharyngeal carcinoma 6-10B cells by targeting miR-4429.Methods The correlations of circFOXP1 and miR-4429 with pathological characteristics of nasopharyngeal carcinoma patients were analyzed.Nasopharyngeal carcinoma 6-10B cells were transfected with si-NC,si-circFOXP1,pcDNA,pcDNA-circFOXP1,miR-NC,miR-4429 mimics,or co-transfected with si-circFOXP1 and anti-miR-NC,or si-circFOXP1 and anti-miR-4429.Quantitative real-time polymerase chain reaction(qRT-PCR)was used to detect circFOXP1 and miR-4429 expression in nasopharyngeal carcinoma tissues.Cell viability,colony formation,migration and invasion abilities were assessed by Cell Counting Kit-8(CCK-8),colony formation,wound healing and Transwell assays.Western blotting was used to detect E-cadherin and N-cadherin protein expression.A dual-luciferase reporter assay verified the targeting relationship between circFOXP1 and miR-4429.Results The expression level of circFOXP1 in nasopharyngeal carcinoma tissues(4.61±0.31)was significantly higher than that in adjacent tissues(1.00±0.05)(P<0.001),while the expression level of miR-4429(0.37±0.03)was significantly lower than that in adjacent tissues(1.00±0.08)(P<0.001).The expression of miR-4429 was correlated with tumor volume and TNM stage(P<0.05),while the expression of circFOXP1 was correlated with TNM stage(P<0.05)but not with tumor volume(P>0.05).Inhibition of circFOXP1 expression or overexpression of miR-4429 reduced cell viability,colony formation number,wound healing rate,invasive cell number and N-cadherin protein expression,while increased E-cadherin protein expression in nasopharyngeal carcinoma 6-10B cells(P<0.05).circFOXP1 targeted and negatively regulated miR-4429 expression.Interference with miR-4429 reversed the inhibitory effects of circFOXP1 silencing on proliferation,migration and invasion of nasopharyngeal carcinoma cells(P<0.05).Conclusion Inhibition of circFOXP1 expression can attenuate the proliferation,migration and invasion of nasopharyngeal carcinoma 6-10B cells by targeting miR-4429.
张燕霞;张冰;丁月梅
新乡市中心医院/新乡医学院第四临床学院 耳鼻喉科(新乡 453000)新乡市中心医院/新乡医学院第四临床学院 耳鼻喉科(新乡 453000)新乡市中心医院/新乡医学院第四临床学院 耳鼻喉科(新乡 453000)
鼻咽癌6-10B细胞circFOXP1miR-4429增殖迁移侵袭
Nasopharyngeal carcinoma 6-10B cellscircFOXP1miR-4429ProliferationMigrationInvasion
《四川大学学报(医学版)》 2026 (3)
692-698,7
This study was supported by the Medical Science and Technology Research Project of Henan Province(No.LHGJ20210911). 河南省医学科技攻关计划项目(No.LHGJ20210911)资助
评论