首页|期刊导航|医学分子生物学杂志|NOP14过表达抑制NRIP1表达及卵巢癌SKOV3细胞的增殖与迁移

NOP14过表达抑制NRIP1表达及卵巢癌SKOV3细胞的增殖与迁移OA

NOP14 Overexpression Inhibits NRIP1 Expression and Proliferation and Migration of Ovarian Cancer SKOV3 Cells

中文摘要英文摘要

目的 探究核仁蛋白14(nucleolar protein 14,NOP14)过表达对卵巢癌SKOV3 细胞增殖与迁移的影响及机制.方法 检测卵巢癌细胞系(SKOV3、A2780、HO-8910、OVCAR)中 NOP14 的表达水平.SKOV3 细胞中转染pcDNA-NOP14 质粒以构建NOP14 过表达细胞系.细胞克隆形成实验和5-乙炔基-2′-脱氧尿苷(5-Ethynyl-2′-deoxyuridine,EdU)染色检测细胞增殖能力.无血清成球培养分析肿瘤干细胞特性.流式细胞术检测CD133 阳性细胞比例.细胞形态学观察及上皮-间质转化(epithelial-mesenchymal transition,EMT)标志蛋白(E-cadherin、N-cadherin、Vimentin)检测评估EMT进程.蛋白质印迹和RT-qPCR检测核受体相互作用蛋白1(nuclear receptor interacting protein 1,NRIP1)及Wnt、β-catenin的表达水平.结果 在卵巢癌细胞系中NOP14 mRNA和蛋白表达均显著低于正常卵巢上皮细胞.NOP14 过表达后抑制SKOV3细胞增殖、干细胞特性及 EMT 转化(间质标志物 N-cadherin、Vimentin 下调,上皮标志物 E-cadherin 上调),以及NRIP1、Wnt和β-catenin的表达水平.结论 NOP14 可负向调控NRIP1 和Wnt及β-catenin的表达,并抑制卵巢癌SKOV3 细胞的增殖、干细胞特性及EMT进程.

Objective To investigate the effect of nucleolar protein 14(NOP14)overexpressi on proliferation and migration of ovarian cancer cells SKOV3 and the underlying mecha-nism.Methods The expression level of NOP14 in ovarian cancer cell lines(SKOV3,A2780,HO-8910,OVCAR)was detected by RT-qPCR and Western blotting.SKOV3 cells were transfected with the pcDNA-NOP14 plasmid.Cell proliferation was detected by colony formation assay and 5-E-thynyl-2′-deoxyuridine(EdU)staining.Tumor stem cell characteristics were analyzed via serum-free sphere formation assay.The proportion of CD133-positive(CD133+)cells was measured by flow cytometry.The epithelial-mesenchymal transition(EMT)process was evaluated by observing cell morphological change and detecting the EMT marker proteins(E-cadherin,N-cadherin,Vim-entin).The expression level of nuclear receptor interacting protein 1(NRIP1),and Wnt/β-catenin pathway proteins were detected by RT-qPCR and Western blotting.Results The expression level of NOP14 was significantly lower in the ovarian cancer cell lines than that in the normal ovarian epithe-lial cells.Overexpression of NOP14 significantly inhibited the proliferation,stem cell characteris-tics,and EMT of SKOV3 cells(mesenchymal markers N-cadherin and Vimentin were downregulat-ed,while the epithelial marker E-cadherin was upregulated).Moreover,Overexpression of NOP14 suppressed the expression of NRIP1,Wnt and β-catenin.Conclusion NOP14 can inhibit the pro-liferation,stem cell characteristics,and EMT process of ovarian cancer SKOV3 cells,and nega-tively regulate the expression of NRIP1,Wnt,β-catenin.

李苓妙;李萍;胡晓丽;王冬梅;武子先

陆军军医大学士官学校附属医院妇产科 石家庄市,050041陆军军医大学士官学校附属医院妇产科 石家庄市,050041陆军军医大学士官学校附属医院妇产科 石家庄市,050041陆军军医大学士官学校附属医院妇产科 石家庄市,050041陆军军医大学士官学校附属医院妇产科 石家庄市,050041

医药卫生

核仁蛋白14卵巢癌核受体相互作用蛋白1细胞增殖上皮-间质转化

nucleolar protein 14ovarian cancernuclear receptor interacting protein 1cell proliferationepithelial-mesenchymal transition

《医学分子生物学杂志》 2026 (1)

67-73,7

河北省2022年度医学科学研究课题(No.20221906) This work was supported by a grant from the Hebei Province 2022 Annual Medical Science Research Topic(No.20221906)

10.3870/j.issn.1672-8009.2026.01.009

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