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miR-125b-5p对人血管瘤内皮细胞HemES增殖和凋亡的影响及其机制
引用本文:王恬,张福林,赵越,郭东栋,杨瑞.miR-125b-5p对人血管瘤内皮细胞HemES增殖和凋亡的影响及其机制[J].中国应用生理学杂志,2021,37(3):247-253.
作者姓名:王恬  张福林  赵越  郭东栋  杨瑞
作者单位:延安市人民医院肿瘤血液科, 陕西 延安 716000
基金项目:*陕西省科技攻关项目(2016SF-138)
摘    要:目的:研究miR-125b-5p对人血管瘤内皮细胞HemECs增殖、凋亡的影响.方法:RT-qPCR检测人血管瘤内皮细胞HemECs及其旁系组织细胞中miR-125b-5p与MCL-1 mRNA的表达;选取HemECs细胞分为对照组、miR-NC 组、miR-125b-5p mimic 组、miR-125b-5p in...

关 键 词:miR-125b-5p  MCL-1  血管瘤  增殖  凋亡

Effects of miR-125b-5p on the proliferation and apoptosis of human hemangioma endothelial cells HemES and its mechanism
WANG Tian,ZHANG Fu-lin,ZHAO Yue,GUO Dong-dong,YANG Rui.Effects of miR-125b-5p on the proliferation and apoptosis of human hemangioma endothelial cells HemES and its mechanism[J].Chinese Journal of Applied Physiology,2021,37(3):247-253.
Authors:WANG Tian  ZHANG Fu-lin  ZHAO Yue  GUO Dong-dong  YANG Rui
Affiliation:Department of Tumor Hematology, Yan'an People's Hospital, Yanan 716000, China
Abstract:Objective: This article mainly studies the effects of miR-125b-5p on the proliferation and apoptosis of human hemangioma endothelial cells HemECs. Methods: RT-qPCR was used to detect the expressions of miR-125b-5p and MCL-1 mRNA in HemECs and collateral cells of human hemangioma endothelial cells. HemECs were selected and divided into control group, miR-NC group, miR-125b-5p mimic group, miR-125b-5p inhibitor group, pc-MCL-1 group, miR-125b-5p+ pc-MCL-1 group, 9 multiple holes in each group. . HemECs were transfected with 100 nmol · L-1 of miR-NC, miR-125b-5p mimic, miR-125b-5p inhibitor, pc-MCL-1 plasmids separately or in combination. MTT method was used to detect the proliferation of HemECs. The apoptosis of HemECs was detected by flow cytometry. Dual luciferase report was used to to detect targeting relationship. The relative expression levels of Ki67, PCNA, cleaved caspase-3, Bax, Bcl-2, p-p70s6k/ p70s6k, p-AKT/AKT, and p-mTOR/mTOR proteins were detected by Western blot. Results: By comparing the expression levels of miR-125b-5p in hemangioma tissues and cells, HemECs cell lines with obvious down-regulation effects were selected for follow-up experiments. Compared with the control group, the proliferation of HemECs and the expressions of Ki67 and PCNA in the miR-125b-5p mimic group were decreased significantly (P<0.01). The apoptotic rate of HemECs and the expression levels of cleaved Caspase-3 and Bax were increased significantly, while the expression of Bcl-2 was decreased significantly (P<0.01). The expression levels of p-AKT/AKT, p-mTOR/mTOR and p-p70S6K/p70S6K were down-regulated significantly (P <0.01); the proliferation of HemECs and the expressions of Ki67 and PCNA in the miR-125b-5p inhibitor group were increased significantly (P <0.01); the apoptosis rate and the expressions of cleaved Caspase-3 and Bax were decreased significantly, and the expression of Bcl-2 was increased (P<0.05, P<0.01). miR-125b-5p targeted down-regulation of MCL-1. Compared with miR-125b-5p mimic group, the proliferation of HemECs and the expressions of Ki67 and PCNA in miR-125b-5p+ pc-MCL-1 group were increased significantly (P<0.01), the apoptosis rate of HemECs and the expressions of cleaved Caspase-3 and Bax were decreased significantly, while the expression of Bcl-2 was increased (P<0.01). The expressions of p-AKT/AKT, p-mTOR/mTOR, and p-p70S6K/p70S6K was also increased significantly (P<0.01). Conclusion: miR-125b-5p inhibits the proliferation of human hemangioma endothelial cells and induces apoptosis. The mechanism may be related to the targeted down-regulation of MCL-1 expression and inhibition of AKT/mTOR pathway activation.
Keywords:miR-125b-5p  MCL-1  hemangioma  proliferation  apoptosis  
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