Suppr超能文献

CpG-寡脱氧核苷酸通过Toll样受体9信号通路和上调Runt相关转录因子3的表达抑制A549肺腺癌细胞的增殖。

CpG-oligodeoxynucleotides suppress the proliferation of A549 lung adenocarcinoma cells via toll-like receptor 9 signaling and upregulation of Runt-related transcription factor 3 expression.

作者信息

Barnie Prince Amoah, Zhang Pan, Lu Ping, Chen Xiaobo, Su Zhaoliang, Wang Shengjun, Xu Huaxi

机构信息

Department of Immunology, School of Medical Science and Laboratory Medicine, Jiangsu University, Zhenjiang, Jiangsu 212013, P.R. China.

Division of Nephrology, Department of Internal Medicine, Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.

出版信息

Biomed Rep. 2014 May;2(3):374-377. doi: 10.3892/br.2014.257. Epub 2014 Mar 18.

Abstract

The aim of the present study was to investigate the effect of CpG-oligodeoxynucelotides (CpG-ODN) on the proliferation of the A549 human lung adenocarcinoma cell line and the expression of Runt-related transcription factor 3 (Runx3) and investigate the association between the toll-like receptor 9 (TLR9) signaling pathway and Runx3 expression during A549 cell proliferation. Different concentrations of CpG-ODN were used in this study to stimulate A549 cells and the expression of Runx3 at the mRNA or protein level was detected by reverse transcription-polymerase chain reaction or western blot analysis. Moreover, Runx3 siRNA was synthesized and transiently transfected into the A549 cells and the MTT assay was used to detect the effects of CpG-ODN on transfected cell growth. Our data demonstrated that CpG-ODN significantly inhibited the proliferation of A549 cells. The expression of Runx3 in the mRNA and protein level was increased in A549 cells stimulated by CpG-ODN. The CpG-ODN-stimulated cell proliferation was significantly inhibited in Runx3 siRNA-transfected A549 cells. In conclusion, CpG-ODN may bind to TLR9, inhibit the proliferation of A549 cells and upregulate the expression of Runx3.

摘要

本研究的目的是探讨CpG-寡脱氧核苷酸(CpG-ODN)对A549人肺腺癌细胞系增殖以及Runt相关转录因子3(Runx3)表达的影响,并研究Toll样受体9(TLR9)信号通路与A549细胞增殖过程中Runx3表达之间的关联。本研究使用不同浓度的CpG-ODN刺激A549细胞,并通过逆转录-聚合酶链反应或蛋白质印迹分析检测Runx3在mRNA或蛋白质水平的表达。此外,合成Runx3 siRNA并将其瞬时转染到A549细胞中,使用MTT法检测CpG-ODN对转染细胞生长的影响。我们的数据表明,CpG-ODN显著抑制A549细胞的增殖。在CpG-ODN刺激的A549细胞中,Runx3在mRNA和蛋白质水平的表达均增加。在Runx3 siRNA转染的A549细胞中,CpG-ODN刺激的细胞增殖受到显著抑制。总之,CpG-ODN可能与TLR9结合,抑制A549细胞的增殖并上调Runx3的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38eb/3990193/8e8d10e5eed0/BR-02-03-0374-g00.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验