文章摘要
范金柱,从 飞,张文韬,田小宁,宋 涛,郭云山.circ_0001461靶向抑制miR-30a-5p对骨肉瘤细胞增殖和凋亡的影响[J].,2022,(8):1413-1418
circ_0001461靶向抑制miR-30a-5p对骨肉瘤细胞增殖和凋亡的影响
The Effect of Circ_0001461 Targeting Inhibition of miR-30a-5p on the Proliferation and Apoptosis of Osteosarcoma Cells
投稿时间:2021-10-31  修订日期:2021-11-27
DOI:10.13241/j.cnki.pmb.2022.08.003
中文关键词: 骨肉瘤  circ_0001461  miR-30a-5p  增殖  凋亡
英文关键词: Osteosarcoma  circ_0001461  miR-30a-5p  Proliferation  Apoptosis
基金项目:西安交通大学基本科研业务费(xzy01201923);陕西省2020年自然科学基础研究计划(2020JM-687)
作者单位E-mail
范金柱 西安交通大学附属红会医院骨显微修复外科 陕西 西安 710054 fmmufjz@163.com 
从 飞 西安交通大学附属红会医院骨显微修复外科 陕西 西安 710054  
张文韬 西安交通大学附属红会医院骨显微修复外科 陕西 西安 710054  
田小宁 西安交通大学附属红会医院骨显微修复外科 陕西 西安 710054  
宋 涛 西安交通大学附属红会医院骨显微修复外科 陕西 西安 710054  
郭云山 西安交通大学附属红会医院脊柱外科 陕西 西安 710054  
摘要点击次数: 658
全文下载次数: 271
中文摘要:
      摘要 目的:探讨circ_0001461对骨肉瘤细胞增殖和凋亡的影响及调控机制。方法:采用实时荧光定量聚合酶反应(qRT-PCR)检测检测circ_0001461在骨肉瘤组织和细胞中的表达水平。在U2OS和HOS细胞中转染sh-NC和sh-circ_0001461后,采用CCK8检测细胞增殖情况,流式细胞术检测细胞凋亡情况,qRT-PCR检测增殖相关分子Ki-67 mRNA的表达水平,Western Blot检测凋亡相关分子Cleaved-caspase-3蛋白的表达水平。采用双荧光素酶报告基因检测circ_0001461和miR-30a-5p的结合情况。结果:circ_0001461在骨肉瘤组织中的表达水平明显高于癌旁正常组织(P<0.05),circ_0001461在骨肉瘤细胞U2OS和HOS中的表达水平均明显高于成骨细胞NHOst(P<0.05)。低表达circ_0001461能够抑制骨肉瘤细胞U2OS和HOS的增殖和增殖相关分子Ki-67的表达(P<0.05);促进骨肉瘤细胞U2OS和HOS的凋亡和凋亡相关分子Cleaved-caspase-3蛋白的表达(P<0.05)。双荧光素酶结果显示circ_0001461能够靶向结合miR-30a-5p。低表达circ_0001461能够促进miR-30a-5p的表达(P<0.05),circ_0001461和miR-30a-5p在骨肉瘤组织中的表达呈负相关(P<0.05)。在U2OS细胞中共转染sh-circ_0001461和miR-30a-5p mimics后能够进一步加强单独转染sh-circ_0001461对U2OS细胞增殖和凋亡的影响(P<0.05);在HOS细胞中共转染sh-circ_0001461和miR-30a-5p inhibitors后能够逆转单独转染sh-circ_0001461对U2OS细胞增殖和凋亡的影响(P>0.05)。结论:circ_0001461在骨肉瘤组织和细胞中明显高表达,低表达circ_0001461能够靶向促进miR-30a-5p的表达进而抑制骨肉瘤细胞增殖和促进细胞凋亡。
英文摘要:
      ABSTRACT Objective: To investigate the effect of circ_0001461 on the proliferation and apoptosis of osteosarcoma cells and its regulatory mechanism. Methods: Real-time fluorescent quantitative polymerase reaction(qRT-PCR) was used to detect the expression level of circ_0001461 in osteosarcoma tissues and cells. After transfection of sh-NC and sh-circ_0001461 in U2OS and HOS cells, CCK8 was used to detect cell proliferation, flow cytometry was used to detect cell apoptosis, qRT-PCR was used to detect the expression level of proliferation-related molecule Ki-67 mRNA, Western Blot was used to detect the expression level of apoptosis-related molecule Cleaved-caspase-3 protein. The dual luciferase reporter gene was used to detect the binding of circ_0001461 and miR-30a-5p. Results: The expression level of circ_0001461 in osteosarcoma tissue was significantly higher than that in normal adjacent tissues(P<0.05), and the expression level of circ_0001461 in osteosarcoma cells U2OS and HOS was significantly higher than that in osteoblast NHOst (P<0.05). Low expression of circ_0001461 could inhibit the proliferation of osteosarcoma cells U2OS and HOS and the expression of proliferation-related molecule Ki-67(P<0.05); promote the apoptosis of osteosarcoma cells U2OS and HOS and the apoptosis-related molecule Cleaved-caspase-3 protein Expression(P<0.05). The results of dual luciferase showed that circ_0001461 could target miR-30a-5p. Low expression of circ_0001461 could promote the expression of miR-30a-5p(P<0.05), and the expression of circ_0001461 and miR-30a-5p in osteosarcoma tissues was negatively correlated (P<0.05). Co-transfection of sh-circ_0001461 and miR-30a-5p mimics in U2OS cells could further enhance the effect of single transfection of sh-circ_0001461 on the proliferation and apoptosis of U2OS cells (P<0.05); co-transfection of sh-circ_0001461 and miR-30a-5p inhibitors in HOS cells could reverse the effect of single transfection sh-circ_0001461 on the proliferation and apoptosis of U2OS cells (P>0.05). Conclusion: circ_0001461 was highly expressed in osteosarcoma tissues and cells. The low expression of circ_0001461 could target the expression of miR-30a-5p to inhibit the proliferation of osteosarcoma cells and promote cell apoptosis.
查看全文   查看/发表评论  下载PDF阅读器
关闭