国家神经系统疾病临床医学研究中心数据管理与共享系统

Data Management And Sharing System of China National Clinical Research Center for Neurological Diseases

RNaseH2A is involved in human gliomagenesis through the regulation of cell proliferation and apoptosis.

第一作者:Bin Dai

通讯作者:Liwei Zhang

RNaseH2A glioma cell proliferation

基本信息

  • 负责人:Bin Dai
  • 数据来源: OTHERS
  • 论文编号:OTHERS20190410
  • 发表时间:2016-07-01

2016-07-01

已发表文章

发表杂志:Oncology Reports

发表类型: Research Article

影响因子(IF): 3.906

PMID: 27176716 Pubmed原文链接 全文下载

主要研究背景及目的

方法

RNaseH2A was silenced in glioblastoma cell lines U87 and U251. Gene expression was assessed in the cells transfected with RNaseH2A shRNA or scramble shRNA by microarrays, validated by quantitative real time PCR. Protein expression was evaluated by western blot analysis. Cell proliferation was assessed by the MTT assay; cell cycle distribution and apoptosis were analyzed by flow cytometry. Finally, the effects of RNaseH2A on colony formation and tumorigenicity were assessed in vitro and in a mouse xenograft model, respectively.

结论

RNaseH2A may be involved in human gliomagenesis, likely by regulating signaling pathways responsible for cell proliferation and apoptosis.

主要结果