期刊文献+

miR-449a过表达抑制人神经母细胞瘤细胞SH-SY5Y增殖并促进其凋亡 被引量:2

Over-expressed miR-449a inhibits proliferation and induces apoptosis of SH-SY5Y cells in vitro
下载PDF
导出
摘要 目的探讨miR-449a对人神经母细胞瘤细胞系SH-SY5Y的增殖和凋亡的影响。方法用Lipofectamine TM2000将miR-449a模似物或miR-449a对照转染至SH-SY5Y细胞,分为空白、miR-449a模似物和miR-449a对照SHSY5Y细胞组;实时荧光定量PCR(q-PCR)检测各组细胞中miR-449a表达;CCK8法检测细胞增殖;流式细胞仪检测细胞凋亡和周期,Western blot检测c-Myc蛋白和Bax/Bcl-2蛋白表达。结果 miR-449a模似物瞬时转染SH-SY5Y细胞后,miR-449a的表达水平明显高于正常对照组(P<0.05);SH-SY5Y细胞增殖能力受到明显抑制(P<0.05);凋亡率明显增加(P<0.05);c-Myc蛋白表达显著降低(P<0.05);细胞促凋亡蛋白Bax表达升高;抗凋亡蛋白Bcl-2表达降低(P<0.05)。结论 miR-449a可通过c-Myc影响SH-SY5Y细胞的增殖和周期,通过调节Bax/Bcl-2影响其凋亡。 Objective To explore neuroblastoma SH-SY5Y cells. Methods effects of miR-449a on the proliferation and apoptosis in human Transferred miR-449a mimics SH-SY5Y cells by LipofectamineTM2000 as experimental group. Cell growth was measured by CCK8 assay, the cell cycle and apoptosis were detected by flow eytometry. Relative expression of e-Mye and Bax/Bel-2 was detected by Western blot. Results Compare to blank and negative control cells, the proliferation of miR-449a mimics SH-SY5Y cells was decreased(P〈0.05). Flow cy- tometry showed that over-expressed miR-449a resulted in an increase of G0/G1 phase and apoptotie cells. The ex- pression of c-Mye showed significant difference (P〈0.05) , Expression of pro-apoptotie protein Bax was increased, and that of anti-apoptotic protein Bcl-2 was decreased(P〈0. 05). Conclusions miR-449a over-expression can in- hibit cell proliferation by regulating cell cycles and induce apoptosis mainly through regulating Bel-2 family proteins expression in SH-SY5Y cells.
出处 《基础医学与临床》 CSCD 2017年第8期1117-1121,共5页 Basic and Clinical Medicine
基金 重庆市卫计委科技项目(zy201602100)
关键词 miRNA—449a SH—SY5Y 增殖 凋亡 细胞周期 miRNA-449a SH-SY5Y proliferation apoptosis cell cycle
  • 相关文献

参考文献5

二级参考文献60

  • 1Jemal A, Bray F, Center M M, et al. Global cancer statistics [J]. CA Cancer J Clin, 2011,61:69-90. 被引量:1
  • 2Wang H X, Li Q, Sharma C, Knoblich K, et al. Tetraspanin protein contributions to cancer [J]. Biochem Soc Trans, 2011, 39(2) : 547-552. 被引量:1
  • 3Jan S, Andreas P, Morten L, et al. Inhibition of microRNA function by antimiR oligonucleotides [J]. Silence, 2012,3 : 1. 被引量:1
  • 4Richard W, Carthew, Erik J, et al. Origins and mechanisms of miRNAs and siRNAs [J]. Cell, 2009,136(4) :642-655. 被引量:1
  • 5Wu W K, Lee C W, Cho C H, et al. MicroRNA dysregulation in gastric cancer: a new player enters the game [J]. Oncogene, 2010,29 : 5761-5771. 被引量:1
  • 6Lize M, Klimke A, Dobbelstein M. MicroRNA-449 in cell fate determination [J ]. Cell Cycle, 2011, 10(17) : 2874-2882. 被引量:1
  • 7Chen C, Ridzon D A, Broomer A J, et al. Real-time quantification of microRNAs by stem-loop RT-PCR [J]. Nucleic Acids Research, 2005,33 (20) : e 179. 被引量:1
  • 8Teng Z, Kuang X Z, Wang J Y, et al. Real-time cell analysis-A new method for dynamic, quantitative measurement of infectious viruses and antiserum neutralizing activity [J]. J Virol Methods, 2013. pii: S0166-0934(13)00 248-6. 被引量:1
  • 9Leemann U, Ruch F. Selective excitation of mithramycin or DAPI fluorescence on double-stained cell nuclei and chromosomes [J]. Histochemistry, 1978,58(4) :329-334. 被引量:1
  • 10Flynt A S, Lai E C. Biological principles of microRNA- mediated regulation: shared themes amid diversity [J]. Nature Reviews Genetics, 2008,9( 11 ) : 831-842. 被引量:1

共引文献13

同被引文献7

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部