孙凯颉,褚 冬,王敏磊,仇 诚,李英斌.慢病毒介导MicroRNA-376b-3p对垂体腺瘤细胞增殖和凋亡的影响及机制探究[J].,2020,(22):4225-4228 |
慢病毒介导MicroRNA-376b-3p对垂体腺瘤细胞增殖和凋亡的影响及机制探究 |
Effect of Lentivirus-mediated MicroRNA-376b-3p on the Proliferation and Apoptosis of Pituitary Adenoma Cells and the Mechanism |
投稿时间:2020-06-23 修订日期:2020-07-18 |
DOI:10.13241/j.cnki.pmb.2020.22.005 |
中文关键词: MicroRNA-376b-3p 靶向 HMGA2 垂体腺瘤 生长 |
英文关键词: Microrna-376b-3p Targeting HMGA2 Pituitary adenoma Growth |
基金项目:江苏省中医药科技项目(YB2017093) |
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中文摘要: |
摘要 目的:探究慢病毒介导MicroRNA-376b-3p对垂体腺瘤增殖和凋亡的影响及其可能的机制。方法:以体外培养的人垂体腺瘤细胞系为研究对象,分别设立为MicroRNA-376b-3p mimics组(对照组)和慢病毒lenti-sh MicroRNA-376b-3p组(药物组),采用MTT法检测MicroRNA-376b-3p对垂体腺瘤细胞增殖的影响,AnnexinV-FITC/PI双染法检测MicroRNA-376b-3p对垂体腺瘤细胞凋亡率的影响,Western blot法检测MicroRNA-376b-3p对高迁移率蛋白A2(HMGA2)、Bcl-2相关X蛋白(Bax)、半胱氨酸天冬氨酸蛋白酶-3(Caspase-3)蛋白表达的影响。结果:(1) 慢病毒介导MicroRNA-376b-3p能够显著抑制垂体腺瘤细胞的增殖(P<0.05);(2)在MicroRNA-376b-3p干预后12 h、24 h以及48 h,垂体腺细胞的凋亡率均明显升高(P<0.05);(3)经MicroRNA-376b-3p转染后,Bax蛋白表达升高,Bcl-2、Caspase-3、Survivin以及HMGA2蛋白表达降低(P<0.05)。结论:慢病毒介导MicroRNA-376b-3p能够明显抑制垂体腺瘤细胞增殖,诱导其凋亡,分析其作用机制可能与下调HMGA2和Survivin表达及上调Bax蛋白表达有关。 |
英文摘要: |
ABSTRACT Objective: To investigate the effect of lentivirus-mediated microrna-376b-3p on the proliferation and apoptosis of pituitary adenomas and its possible mechanism. Methods: Taking human pituitary adenoma cell lines cultured in vitro as the research object, the microRNA-376b-3p mimics group (control group) and lenti-sh MicroRNA-376b-3p group (drug group) were established respectively, and the MTT method was used to detect MicroRNA-376b-3p on the proliferation of pituitary adenoma cells, the AnnexinV-FITC/PI double staining method was used to detect the effect of MicroRNA-376b-3p on the apoptosis rate of pituitary adenoma cells, and the Western blot method was used to detect the effect of MicroRNA-376b-3p on HMGA2, Bax, Caspase-3 protein expression. Results: (1) Lentivirus-mediated Microrna-376b-3p could significantly inhibit the proliferation of pituitary adenoma cells (P<0.05). (2) At 12, 24 and 48 h after microrna-376b-3p intervention, the apoptosis rate of pituitary gland cells in the control group was significantly lower than that in the drug group (P<0.05). (3) After transfection with microrna-376b-3p transformation, the expression of Bax protein increased, and the expression of Bcl-2, Caspase-3, Survivin and HMGA2 protein decreased (P<0.05). Conclusion: Lentivirus-mediated Microrna-376b-3p could significantly inhibit the proliferation of pituitary adenoma cells and induce apoptosis. The mechanism of microrna-376b-3p may be related to its targeted down-regulation of HMGA2 expression, up-regulation of Bax protein expression and regulation of survivin protein expression. |
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