微小RNA-155对骨肉瘤细胞体外增殖的影响

Chuangjian Wang, Xiaobo Zhang, Hong-jian Liu, Chunlin Zhang, Xue-ping Wu, Yan Zhang
{"title":"微小RNA-155对骨肉瘤细胞体外增殖的影响","authors":"Chuangjian Wang, Xiaobo Zhang, Hong-jian Liu, Chunlin Zhang, Xue-ping Wu, Yan Zhang","doi":"10.3760/CMA.J.ISSN.1001-9030.2020.01.032","DOIUrl":null,"url":null,"abstract":"Objective \nTo explore the effects of microRNA-155 (miR-155) expression on growth of osteosarcoma cells and the action mechanism. \n \n \nMethods \nNormal osteoblasts served as the control group and osteosarcoma cells as the experimental group. MiR-155 levels were examined by real-time quantitative polymerase chain reaction (Real-time PCR). The effects of miR-155 on proliferation of osteosarcoma cells and apoptosis were detected by cell counting kit-8 (CCK-8) and flow cytometry assays respectively. Real-time PCR and Western blotting were applied to investigate the target gene of miR-155 in osteosarcoma cells. T test was used for comparison between the two groups, and anova was used for comparison between multiple groups, P<0.05 was considered to be statistically significant. \n \n \nResults \nMiR-155 expression was significantly up-regulated in osteosarcoma cells (U2OS, Saox-2 and MG-63) (5.10±0.32, 6.82±0.48 and 10.12±0.39) as compared with their matched normal parts (1.01±0.13, t=13.100, P<0.01). CCK-8 indicated that, compared with the negative control group (0.37±0.02, 0.58±0.02, 0.80±0.04), the A values of MG-63 cells were 0.49±0.03, 0.77±0.03, 0.93±0.02, respectively, at 48, 72 and 96 h after transfection with miR-155, and their proliferation capacity was significantly enhanced (t=11.200, P<0.05). Moreover, 48 h after transfeetion, the apoptosis rate of MG-63 cells in miR-155 treatment group was (0.90±0.13)%, significantly lower than in miR-control group [(5.92±0.80)%, t=17.900, P<0.05]. \n \n \nConclusion \nOur data revealed that miR-155 may function as an oncogene in osteosarcoma development and it may also provide a therapeutic strategy for controlling osteosarcoma progression. \n \n \nKey words: \nOsteosarcoma; MicroRNA-155","PeriodicalId":10065,"journal":{"name":"中华实验外科杂志","volume":"37 1","pages":"112-114"},"PeriodicalIF":0.0000,"publicationDate":"2020-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of microRNA-155 on proliferation of osteosarcoma cells in vitro\",\"authors\":\"Chuangjian Wang, Xiaobo Zhang, Hong-jian Liu, Chunlin Zhang, Xue-ping Wu, Yan Zhang\",\"doi\":\"10.3760/CMA.J.ISSN.1001-9030.2020.01.032\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective \\nTo explore the effects of microRNA-155 (miR-155) expression on growth of osteosarcoma cells and the action mechanism. \\n \\n \\nMethods \\nNormal osteoblasts served as the control group and osteosarcoma cells as the experimental group. MiR-155 levels were examined by real-time quantitative polymerase chain reaction (Real-time PCR). The effects of miR-155 on proliferation of osteosarcoma cells and apoptosis were detected by cell counting kit-8 (CCK-8) and flow cytometry assays respectively. Real-time PCR and Western blotting were applied to investigate the target gene of miR-155 in osteosarcoma cells. T test was used for comparison between the two groups, and anova was used for comparison between multiple groups, P<0.05 was considered to be statistically significant. \\n \\n \\nResults \\nMiR-155 expression was significantly up-regulated in osteosarcoma cells (U2OS, Saox-2 and MG-63) (5.10±0.32, 6.82±0.48 and 10.12±0.39) as compared with their matched normal parts (1.01±0.13, t=13.100, P<0.01). CCK-8 indicated that, compared with the negative control group (0.37±0.02, 0.58±0.02, 0.80±0.04), the A values of MG-63 cells were 0.49±0.03, 0.77±0.03, 0.93±0.02, respectively, at 48, 72 and 96 h after transfection with miR-155, and their proliferation capacity was significantly enhanced (t=11.200, P<0.05). Moreover, 48 h after transfeetion, the apoptosis rate of MG-63 cells in miR-155 treatment group was (0.90±0.13)%, significantly lower than in miR-control group [(5.92±0.80)%, t=17.900, P<0.05]. \\n \\n \\nConclusion \\nOur data revealed that miR-155 may function as an oncogene in osteosarcoma development and it may also provide a therapeutic strategy for controlling osteosarcoma progression. \\n \\n \\nKey words: \\nOsteosarcoma; MicroRNA-155\",\"PeriodicalId\":10065,\"journal\":{\"name\":\"中华实验外科杂志\",\"volume\":\"37 1\",\"pages\":\"112-114\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中华实验外科杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3760/CMA.J.ISSN.1001-9030.2020.01.032\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中华实验外科杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/CMA.J.ISSN.1001-9030.2020.01.032","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的探讨microRNA-155 (miR-155)表达对骨肉瘤细胞生长的影响及其作用机制。方法以正常成骨细胞为对照组,以骨肉瘤细胞为实验组。采用实时定量聚合酶链反应(real-time PCR)检测MiR-155水平。通过细胞计数试剂盒-8 (CCK-8)和流式细胞术检测miR-155对骨肉瘤细胞增殖和凋亡的影响。采用Real-time PCR和Western blotting检测miR-155靶基因在骨肉瘤细胞中的表达。两组间比较采用T检验,多组间比较采用方差分析,P<0.05为差异有统计学意义。结果MiR-155在骨肉瘤细胞(U2OS、Saox-2和MG-63)中的表达水平(5.10±0.32、6.82±0.48和10.12±0.39)明显高于正常组(1.01±0.13,t=13.100, P<0.01)。CCK-8显示,转染miR-155后48、72、96 h MG-63细胞的A值分别为0.49±0.03、0.77±0.03、0.93±0.02,与阴性对照组(0.37±0.02、0.58±0.02、0.80±0.04)比较,增殖能力显著增强(t=11.200, P<0.05)。转染48 h后,miR-155处理组MG-63细胞凋亡率为(0.90±0.13)%,显著低于miR-155对照组[(5.92±0.80)%,t=17.900, P<0.05]。我们的数据显示miR-155可能在骨肉瘤的发展中作为癌基因发挥作用,它也可能为控制骨肉瘤的进展提供治疗策略。关键词:骨肉瘤;微rna - 155
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Effect of microRNA-155 on proliferation of osteosarcoma cells in vitro
Objective To explore the effects of microRNA-155 (miR-155) expression on growth of osteosarcoma cells and the action mechanism. Methods Normal osteoblasts served as the control group and osteosarcoma cells as the experimental group. MiR-155 levels were examined by real-time quantitative polymerase chain reaction (Real-time PCR). The effects of miR-155 on proliferation of osteosarcoma cells and apoptosis were detected by cell counting kit-8 (CCK-8) and flow cytometry assays respectively. Real-time PCR and Western blotting were applied to investigate the target gene of miR-155 in osteosarcoma cells. T test was used for comparison between the two groups, and anova was used for comparison between multiple groups, P<0.05 was considered to be statistically significant. Results MiR-155 expression was significantly up-regulated in osteosarcoma cells (U2OS, Saox-2 and MG-63) (5.10±0.32, 6.82±0.48 and 10.12±0.39) as compared with their matched normal parts (1.01±0.13, t=13.100, P<0.01). CCK-8 indicated that, compared with the negative control group (0.37±0.02, 0.58±0.02, 0.80±0.04), the A values of MG-63 cells were 0.49±0.03, 0.77±0.03, 0.93±0.02, respectively, at 48, 72 and 96 h after transfection with miR-155, and their proliferation capacity was significantly enhanced (t=11.200, P<0.05). Moreover, 48 h after transfeetion, the apoptosis rate of MG-63 cells in miR-155 treatment group was (0.90±0.13)%, significantly lower than in miR-control group [(5.92±0.80)%, t=17.900, P<0.05]. Conclusion Our data revealed that miR-155 may function as an oncogene in osteosarcoma development and it may also provide a therapeutic strategy for controlling osteosarcoma progression. Key words: Osteosarcoma; MicroRNA-155
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
18226
期刊介绍:
期刊最新文献
Application of polybrene to increase transfection efficiency of lentiviral vector in bone marrow derived dendritic cells MicroRNA-224 mediates lipopolysaccharide-induced injury of pulmonary microvascular endothelium cells via regulating p21 Expression and clinical significance of circulating microRNA-375 and tissue Yes-associated protein 1 in colorectal cancer patients Expression and prognosis of N-α-acetyltransferase gene 10 in breast cancer Expression of human cartilage glycoprotein 39 in peripheral blood and tissues in renal cell carcinoma
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1