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首页|期刊导航|河北医学|circ-RBM33靶向miR-383-3p/CKS1B轴抑制鼻咽癌细胞的增殖和转移

circ-RBM33靶向miR-383-3p/CKS1B轴抑制鼻咽癌细胞的增殖和转移OACSTPCD

circ-RBM33 Targets the miR-383-3p/CKS1B Axis to Inhibit Proliferation and Invasion of Nasopharyngeal Carcinoma Cells

中文摘要英文摘要

目的:探究circ-RBM33 能否靶向 miR-383-3p/CKS1B 轴抑制鼻咽癌细胞的增殖和侵袭.方法:qRT-PCR检测CNE1 和HNEpC细胞中circ-RBM33、miR-383-3p 表达.将CNE1 细胞随机分为si-NC组、si-RBM33 组、miR-NC组、miR-383-3p 组和 si-RBM33+anti-miR-383-3p 组.分别检测细胞增殖(CCK-8 法)、侵袭(Transwell法)和迁移(划痕实验)及细胞中 CKS1B 蛋白表达(蛋白质印迹法);荧光素酶活性实验检测circ-RBM33 和 miR-383-3p/CKS1B 的靶向关系.结果:人鼻咽癌细胞CNE1 中circ-RBM33 相对表达量高于人鼻黏膜上皮细胞HNEpC,miR-383-3p 相对表达量低于人鼻黏膜上皮细胞HNEpC(P<0.05).si-RBM33 组 CNE1 细胞中 circ-RBM3 相对表达量、细胞存活率、细胞侵袭数目、细划痕愈合率及细胞中CKS1B蛋白表达均低于 si-NC 组(P<0.05);si-RBM33+anti-miR-383-3p组 CNE1 细胞存活率、细胞侵袭数目、细胞划痕愈合率及细胞中 CKS1B 蛋白表达均高于 si-RBM33 组(P<0.05).miR-383-3p 组 CNE1 细胞中 miR-383-3p 相对表达量明显增加,细胞存活率、细胞侵袭数目、细划痕愈合率及细胞中CKS1B蛋白表达均低于miR-NC 组(P<0.05).转染 WT-circ-RBM33/CKS1B时miR-383-3p组荧光素酶活性明显低于 miR-NC 组(P<0.0001).结论:敲减 circ-RBM33 可能通过上调miR-383-3p表达,进而抑制CKS1B表达来抑制鼻咽癌细胞的增殖、侵袭和迁移.

Objective:To investigate whether circ-RBM33 can target the miR-383-3p/CKS1B axis to inhibit the proliferation and invasion of nasopharyngeal carcinoma cells.Methods:qRT-PCR was used to de-tect the expression of circ-RBM33 and miR-383-3p in CNE1 and HNEpC cells.CNE1 cells were randomly divided into si-NC group,si-RBM33 group,miR-NC group,miR-383-3p group,and si-RBM33+anti-miR-383-3p group.Cell proliferation(CCK-8 assay),invasion(Transwell assay),migration(scratch as-say),and expression of CKS1B protein in cells(Western blot)were detected.Luciferase activity assay was performed to determine the targeting relationship between circ-RBM33 and miR-383-3p/CKS1B.Results:The relative expression of circ-RBM33 in human nasopharyngeal carcinoma CNE1 cells was higher than that in human nasopharyngeal mucosal epithelial HNEpC cells,while the relative expression of miR-383-3p was lower than that in HNEpC cells(P<0.05).In the si-RBM33 group,the relative expression of circ-RBM33 in CNE1 cells,cell viability,number of invading cells,scratch closure rate,and expression of CKS1B protein in cells were lower than those in the si-NC group(P<0.05).In the si-RBM33+anti-miR-383-3p group,the cell viability,number of invading cells,scratch closure rate,and expression of CKS1B protein in cells were higher than those in the si-RBM33 group(P<0.05).In the miR-383-3p group,the relative expres-sion of miR-383-3p in CNE1 cells was significantly increased,while cell viability,number of invading cells,scratch closure rate,and expression of CKS1B protein in cells were lower than those in the miR-NC group(P<0.05).Transfection with WT-circ-RBM33/CKS1B resulted in significantly lower luciferase activity in the miR-383-3p group than in the miR-NC group(P<0.0001).Conclusion:Knockdown of circ-RBM33 may inhibit the proliferation,invasion,and migration of nasopharyngeal carcinoma cells by upregulating miR-383-3p expression and subsequently suppressing CKS1B expression.

周广全;孙相波;卢海波;赵松

江苏省盐城市第一人民医院耳鼻咽喉科,江苏 盐城 224001

鼻咽癌circ-RBM33miR-383-3p/CKS1B轴增殖侵袭

Nasopharyngeal carcinomacirc-RBM33miR-383-3p/CKS1B axisProlifera-tionInvasion

《河北医学》 2024 (006)

881-886 / 6

江苏省卫生健康委员会课题项目,(编号:ZD20210048)

10.3969/j.issn.1006-6233.2024.06.01

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