MicroRNA-92b suppresses proliferation of papillary thyroid cancer cells by regulating ilent information regulator 1 gene expression

W. Di, H. Ji, Qinghuai Li
{"title":"MicroRNA-92b suppresses proliferation of papillary thyroid cancer cells by regulating ilent information regulator 1 gene expression","authors":"W. Di, H. Ji, Qinghuai Li","doi":"10.3760/CMA.J.ISSN.1001-9030.2019.12.012","DOIUrl":null,"url":null,"abstract":"Objective \nTo investigate the regulating effects of microRNA (miRNA, miR)-122 on the expression of ilent information regulator 1 (SIRT1), and the proliferation abilities of papillary thyroid cancer cells. \n \n \nMethods \nReal-time quantitative polymerase chain reaction (Real-time PCR) was used to observe the expression of miR-122 in papillary thyroid carcinoma and adjacent tissues and to analyze its correlation with SIRT1 expression. After transfecting miR-122 mimics into human papillary thyroid carcinoma cell line TPC-1, the dual luciferase reporter gene assay was used to observe the regulation of miR-122 on SIRT1 gene. The effect of miR-122 on the proliferation of thyroid cancer cells was observed by CCK-8 assay. At the same time, the overexpressed SIRT1 plasmid was co-transfected into TPC-1 cells, and then the effect of miR-122 and SIRT1 expression on the proliferation of papillary thyroid carcinoma cells was detected by CCK-8 assay. Analysis was performed using GraphPad Prism 7.0 statistical software. Correlation analysis was performed using Spearman rank correlation analysis. Student’s t test was used to compare the two sample means. \n \n \nResults \nCompared with adjacent tissues (1.20±0.15), the expression level of miR-122 (3.06±0.26) in papillary thyroid carcinoma was significantly down-regulated, and the difference was statistically significant (t=5.972, P<0.01). Correlation analysis showed that miR-122 was negatively correlated with SIRT1 mRNA expression (r=-0.621, P<0.01). The relative luciferase activity of SIRT1 in miR-122 mimics transfection group was significantly lower than that in the control group, and the difference was statistically significant (t=17.730, P<0.01). The cell proliferation ability of miR-122 mimics group was significantly lower than that of the control group, and the difference was statistically significant (t=3.991, P<0.01). After co-transfection of the SIRT1 overexpression plasmid, the inhibition of the proliferation of thyroid papillary carcinoma cells by miR-122 mimics was reversed. \n \n \nConclusion \nmiR-122 can inhibit the proliferation of papillary thyroid cancer cells, and its mechanism may be related to the targeted inhibition of SIRT1 expression. \n \n \nKey words: \nMicroRNA-122; Ilent information regulator 1; Papillary thyroid cancer; Proliferation","PeriodicalId":10065,"journal":{"name":"中华实验外科杂志","volume":"36 1","pages":"2167-2169"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-08","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.1001-9030.2019.12.012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective To investigate the regulating effects of microRNA (miRNA, miR)-122 on the expression of ilent information regulator 1 (SIRT1), and the proliferation abilities of papillary thyroid cancer cells. Methods Real-time quantitative polymerase chain reaction (Real-time PCR) was used to observe the expression of miR-122 in papillary thyroid carcinoma and adjacent tissues and to analyze its correlation with SIRT1 expression. After transfecting miR-122 mimics into human papillary thyroid carcinoma cell line TPC-1, the dual luciferase reporter gene assay was used to observe the regulation of miR-122 on SIRT1 gene. The effect of miR-122 on the proliferation of thyroid cancer cells was observed by CCK-8 assay. At the same time, the overexpressed SIRT1 plasmid was co-transfected into TPC-1 cells, and then the effect of miR-122 and SIRT1 expression on the proliferation of papillary thyroid carcinoma cells was detected by CCK-8 assay. Analysis was performed using GraphPad Prism 7.0 statistical software. Correlation analysis was performed using Spearman rank correlation analysis. Student’s t test was used to compare the two sample means. Results Compared with adjacent tissues (1.20±0.15), the expression level of miR-122 (3.06±0.26) in papillary thyroid carcinoma was significantly down-regulated, and the difference was statistically significant (t=5.972, P<0.01). Correlation analysis showed that miR-122 was negatively correlated with SIRT1 mRNA expression (r=-0.621, P<0.01). The relative luciferase activity of SIRT1 in miR-122 mimics transfection group was significantly lower than that in the control group, and the difference was statistically significant (t=17.730, P<0.01). The cell proliferation ability of miR-122 mimics group was significantly lower than that of the control group, and the difference was statistically significant (t=3.991, P<0.01). After co-transfection of the SIRT1 overexpression plasmid, the inhibition of the proliferation of thyroid papillary carcinoma cells by miR-122 mimics was reversed. Conclusion miR-122 can inhibit the proliferation of papillary thyroid cancer cells, and its mechanism may be related to the targeted inhibition of SIRT1 expression. Key words: MicroRNA-122; Ilent information regulator 1; Papillary thyroid cancer; Proliferation
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
MicroRNA-92b通过调控沉默信息调控因子1基因表达抑制甲状腺乳头状癌细胞增殖
目的探讨微小RNA(miRNA,miR)-122对癌症乳头状细胞沉默信息调节因子1(SIRT1)表达及增殖能力的调节作用。方法采用实时定量聚合酶链反应(Real-time PCR)技术,观察miR-122在甲状腺乳头状癌及癌旁组织中的表达,并分析其与SIRT1表达的相关性。将miR-122模拟物转染人甲状腺乳头状癌细胞系TPC-1后,使用双荧光素酶报告基因分析来观察miR-122对SIRT1基因的调节。通过CCK-8测定观察了miR-122对甲状腺癌症细胞增殖的影响。同时,将过表达的SIRT1质粒共转染到TPC-1细胞中,然后通过CCK-8检测miR-122和SIRT1表达对甲状腺乳头状癌细胞增殖的影响。使用GraphPad Prism 7.0统计软件进行分析。相关分析采用Spearman秩相关分析。学生t检验用于比较两个样本的平均值。结果miR-122在甲状腺乳头状癌中的表达水平(3.06±0.26)明显低于癌旁组织(1.20±0.15),相关分析显示,miR-122与SIRT1 mRNA表达呈负相关(r=-0.621,P<0.01)。miR-122模拟物转染组SIRT1的相对荧光素酶活性显著低于对照组,miR-122模拟物组的细胞增殖能力显著低于对照组,差异具有统计学意义(t=3.991,P<0.01)。SIRT1过表达质粒共转染后,miR-122模拟物对甲状腺乳头状癌细胞增殖的抑制作用被逆转。结论miR-122可抑制甲状腺乳头状癌症细胞增殖,其机制可能与靶向抑制SIRT1表达有关。关键词:MicroRNA-122;Ilent信息调节器1;乳头状甲状腺癌症;扩散
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 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
Adenosine A1R/A3R agonist AST-004 reduces brain infarction in mouse and rat models of acute ischemic stroke. 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
×
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