首页|期刊导航|山东医药|miR-21低表达对垂体瘤细胞系RC-4BC增殖、凋亡的影响及与PTEN靶向关系

miR-21低表达对垂体瘤细胞系RC-4BC增殖、凋亡的影响及与PTEN靶向关系OACSTPCD

Effects of low expression of miR-21 on proliferation and apoptosis of pituitary tumor cell line RC-4BC and its targeting relationship with PTEN

中文摘要英文摘要

目的 观察微小RNA-21(miR-21)低表达对垂体瘤细胞系RC-4BC增殖、凋亡的影响,并分析其与第10号染色体丢失的张力蛋白同源磷酸酶基因(PTEN)的靶向关系.方法 取对数生长期的RC-4BC细胞分为两组,沉默组转染miR-21抑制物miR-21 inhibitor,阴性对照组转染抑制物阴性对照NC-inhibitor,采用RT-PCR法检测miR-21、第10号染色体丢失的张力蛋白同源磷酸酶基因(PTEN)mRNA,采用CCK8实验观察两组细胞增殖能力(以OD值表示),采用平板克隆实验观察两组细胞集落形成能力(以集落形成数表示),采用流式细胞术观察两组细胞凋亡率并观察细胞周期分布情况.收集RC-4BC细胞制备单细胞悬液,分别将miR-21 mimics或NC-mimics与PTEN-WT或PTEN-MUT共转染至RC-4BC细胞,转染后细胞标记为miR-21 mimics+PTEN-WT组、NC-mimics+PTEN-WT组、miR-21 mimics+PTEN-MUT组、NC-mimics+PTEN-MUT组,采用双荧光素酶报告基因实验验证miR-21与PTEN的靶向关系.结果 沉默组RC-4BC细胞中miR-21、PTEN mRNA相对表达量分别为0.30±0.08、2.89±0.14,阴性对照组RC-4BC细胞中miR-21、PTEN mRNA相对表达量分别为1.01±0.02、0.99±0.03,两组相比,P均<0.05.沉默组RC-4BC细胞24 h、48 h、72 h时OD值均低于阴性对照组(P均<0.05).沉默组RC-4BC细胞集落形成数低于阴性对照组(P<0.05).沉默组RC-4BC细胞凋亡率高于阴性对照组(P<0.05).沉默组RC-4BC细胞G0/G1期占比65.65%±7.82%、S期占比19.25%±3.70%,阴性对照组RC-4BC细胞G0/G1 期占比45.62%±5.03%、S期占比35.72%±4.67%,两组相比,P均<0.05.miR-21 mimics+PTEN-WT组、NC-mimics+PTEN-WT组、miR-21 mimics+PTEN-MUT组、NC-mimics+PTEN-MUT组细胞的相对荧光素酶活性分别为0.39±0.07、1.02±0.03、1.01±0.04、1.00±0.03,其中miR-21 mimics+PTEN-WT组相对荧光素酶活性与其他各组相比,P均<0.05.结论 沉默miR-21能够移至垂体瘤细胞系RC-4BC的增殖、促进其凋亡,其机制可能与靶向调控PTEN基因有关.

Objective To investigate the effects of low expression of microRNA-21(miR-21)on the proliferation and apoptosis of pituitary tumor cell line RC-4BC,and to analyze its targeting relationship with phosphatase and tensin homolog deleted on chromosome ten(PTEN).Methods RC-4BC cells in the logarithmic growth phase were divided into two groups.Cells in the silence group were transfected with miR-21 inhibitor,while cells in the negative control group were transfected with inhibitor negative control NC-inhibitor.RT-PCR was used to detect the mRNA of miR-21 and PTEN.CCK8 assay was used to observe the cell proliferation ability of the two groups(expressed by OD value),plate cloning assay was used to observe the cell colony formation ability of the two groups(expressed by colony formation number),flow cytome-try was used to observe the apoptosis rates of the two groups and to observe the cell cycle distribution.Single cell suspension was prepared from RC-4BC cells,and miR-21 mimics or NC-mimics were co-transfected into RC-4BC cells with PTEN-WT or PTEN-MUT,respectively.After transfection,the cells were labeled as the miR-21 mimics+PTEN-WT group,NC-mim-ics+PTEN-WT group,miR-21 mimics+PTEN-MUT group,and NC-mimics+PTEN-MUT group,respectively.The dual lu-ciferase reporter gene assay was used to verify the targeting relationship between miR-21 and PTEN.Results The relative expression levels of miR-21 and PTEN mRNA in RC-4BC cells of the silence group were 0.30±0.08 and 2.89±0.14,re-spectively,while those in the negative control group were 1.01±0.02 and 0.99±0.03,respectively,with statistically sig-nificant differences(all P<0.05).The OD values of RC-4BC cells of the silence group were lower than those of the nega-tive control group at 24,48,and 72 h(all P<0.05).The number of colony formation of RC-4BC cells in the silence group was smaller than that in the negative control group(P<0.05).The apoptosis rate of RC-4BC cells in the silence group was higher than that in the negative control group(P<0.05).The proportions of cells in the G0/G1 phase and S phase were 65.65%±7.82%and 19.25%±3.70%,in the silence group,respectively,versus 45.62%±5.03%and 35.72%±4.67%,in the negative control group,respectively,with statistically significant differences(all P<0.05).The relative luciferase activity of the miR-21 mimics+PTEN-WT group,NC-mimics+PTEN-WT group,miR-21 mimics+PTEN-MUT group,and NC-mimics+PTEN-MUT group was 0.39±0.07,1.02±0.03,1.01±0.04,and 1.00±0.03,respectively,and significant difference was found in the relative luciferase activity between the miR-21 mimics+PTEN-WT group and the other groups(all P<0.05).Conclusion Silencing miR-21 can inhibit the proliferation and promote apoptosis of RC-4BC cells in pi-tuitary tumor cell line,and its mechanism may be related to the targeted regulation of PTEN gene.

宋志远;任洪波;韩晓正;牛国栋

邯郸市中心医院神经外三科,河北邯郸 056009

临床医学

微小RNA-21垂体瘤RC-4BC细胞第10号染色体丢失的张力蛋白同源磷酸酶基因细胞增殖细胞凋亡细胞周期

microRNA-21pituitary tumorRC-4BC cellsphosphatase and tensin homolog deleted on chromo-some tencell proliferationapoptosiscell cycle

《山东医药》 2024 (009)

24-28 / 5

河北省医学科学研究课题计划项目(20200194).

10.3969/j.issn.1002-266X.2024.09.006

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