期刊文献+

miR-199a-5p调控DDR1抑制人脑胶质瘤细胞增殖和迁移 被引量:4

miR-199a-5p regulates DDR1 to inhibit proliferation and migration of human glioma cells
下载PDF
导出
摘要 目的初步探究miR-199a-5p对人脑胶质瘤细胞增殖和迁移的影响。方法选取U251细胞为实验对象,构建miR-199a-5p过表达U251细胞株。实验分组:对照组(无转染的U251细胞,Control)、阴性对照组(转染空载体质粒U251细胞,NC)以及实验组(转染miR-199a-5p成熟模拟物,mimics)。实时荧光定量PCR检测各组细胞miR-199a-5p表达;CCK-8检测转染miR-199a-5p后细胞增殖;细胞划痕实验与Transwell迁移实验检测各组U251迁移情况;Western blot检测DDR1表达;构建DDR1过表达U251细胞株,检测DDR1过表达对转染miR-199a-5p的U251细胞增殖和迁移的影响。结果mimics组细胞miR-199a-5p水平高于control组(P<0.01),细胞活力降低(P<0.01),增殖能力减弱(P<0.01)。转染miR-199a-5p组细胞DDR1表达水平降低(P<0.01)。与mimins组相比,转染pcDNA3.1-DDR1组能够上调DDR1(P<0.01),增加细胞活力,促进细胞增殖(P<0.05或P<0.01)。结论miR-199a-5p能够下调DDR1表达,抑制人脑胶质瘤细胞增殖和迁移。 Aim To investigate the effect of miR-199a-5p on the proliferation and migration of human glioma cells.Methods U251 cells were selected as experimental subjects to construct a U251 cell line overexpressing miR-199a-5p.The experiment was divided into:control group(U251 cells without transfection,Control),negative control group(transfected with empty vector plasmid U251 cells,NC)and experimental group(transfected with miR-199a-5p mature mimics,mimics).Real-time fluorescent quantitative PCR was used to detect the expression of miR-199a-5p in each group;CCK-8 was used to detect the proliferation of cells transfected with miR-199a-5p;the cell scratch test and Transwell migration test were used to detect the migration of U251 in each group;Western blot was applied to detect DDR1 expression;a U251 cell line overexpressing DDR1 was constructed to detect the effect of overexpression of DDR1 on the proliferation and migration of U251 cells transfected with miR-199a-5p.Results The level of miR-199a-5p in mimics group was significantly higher than that in control group(P<0.01),the cell viability was reduced(P<0.01),and the proliferation ability was weakened(P<0.01).The expression of DDR1 in miR-199a-5p group cells was significantly reduced(P<0.01).Compared with mimincs group,the pcDNA3.1-DDR1 transfected group could up-regulate DDR1(P<0.01),increase cell viability,and promote cell proliferation(P<0.05 or P<0.01).Conclusions miR-199a-5p can down-regulate the expression of DDR1 and inhibit the proliferation and migration of human glioma cells.
作者 闫兆月 高玉帅 贾玉龙 步星耀 YAN Zhao-yue;GAO Yu-shuai;JIA Yu-long;BU Xing-yao(Henan Provincial People’s Hospital,Zhengzhou 450008,China)
出处 《中国药理学通报》 CAS CSCD 北大核心 2021年第5期687-692,共6页 Chinese Pharmacological Bulletin
基金 河南省医学科技攻关计划项目(No 192102310126)。
关键词 胶质瘤 增殖 迁移 miR-199a-5p 盘状结构域受体1 U251 glioma proliferation migration miR-199a-5p discoid domain receptor 1 U251
  • 相关文献

参考文献2

二级参考文献35

  • 1Mishra PJ,Bertino JR.MicroRNA polymorphisms:the future of pharmacogenomics,molecular epidemiology and individualized medicine.Pharmacogenomics,2009,10(3):399-416.
  • 2Horikawa Y,Wood CG,Yang HS,Zhao H,Ye YQ,Gu J,Lin J,Habuchi T,Wu XF.Single nucleotide polymorphisms of microRNA machinery genes modify the risk of renal cell carcinoma.Clin Cancer Res,2008,14(23):7956-7962.
  • 3Yang HS,Dinney CP,Ye YQ,Zhu Y,Grossman HB,Wu XF.Evaluation of genetic variants in microRNA-related genes and risk of bladder cancer.Cancer Res,2008,68(7):2530-2537.
  • 4Gottwein E,Cai XZ,Cullen BR.A novel assay for viral microRNA function identifies a single nucleotide polymorphism that affects Drosha processing.J Virol,2006,80(11):5321-5326.
  • 5Duan RH,Pak CH,Jin P.Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA.Hum Mol Genet,2007,16(9):1124-1131.
  • 6Wu MQ,Jolicoeur N,Li Z,Zhang LH,Fortin Y,L'Abbe D,Yu ZB,Shen SH.Genetic variations of microRNAs in human cancer and their effects on the expression of miRNAs.Carcinogenesis,2008,29(9):1710-1716.
  • 7Mencía (A),Modamio-Hφybjφr S,Redshaw N,Morín M,Mayo-Merino F,Olavarrieta L,Aguirre LA,del Castillo I,Steel KP,Dalmay T,Moreno F,Moreno-Pelayo M.Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.Nat Genet,2009,41(5):609-613.
  • 8Li W,Duan R,Kooy F,Sherman SL,Zhou W,Jin P.Germline mutation of microRNA-125a is associated with breast cancer.J Med Genet,2009,46(5):358-360.
  • 9Pfister S,Remke M,Castoldi M,Bai AHC,Muckenthaler MU,Kulozik A,von Deimling A,Pscherer A,Lichter P,Korshunov A.Novel genomic amplification targeting the microRNA cluster at 19q13.42 in a pediatric embryonal tumor with abundant neuropil and true rosettes.ActaNeuropathol,2009,117(4):457-464.
  • 10Bandi N,Zbinden S,Gugger M,Arnold M,Kocher V,Hasan L,Kappeler A,Brunner T,Vassella E.miR-15a and miR-16 are implicated in cell cycle regulation in a Rb-dependent manner and are frequently deleted or down-regulated in non-small cell lung cancer.Cancer Res,2009,69(13):5553-5559.

共引文献13

同被引文献36

引证文献4

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