| Literature DB >> 28859546 |
Zaishun Jin1, Tao Zhan2, Jing Tao3, Biao Xu4, Huizhe Zheng2, Yongxia Cheng2, Bin Yan2, Hongwei Wang2, Guoqiang Lu5, Ying Lin6, Sufen Guo1,2.
Abstract
The function of microRNA-34a (miR-34a) in transdifferentiation of glioma stem cells (GSCs) into vascular endothelial cells (VECs) was explored by focusing on Notch ligand Delta-like 1 (Dll1). MiR-34a mimics was transfected into CD133 + glioma cell U251. The angiogenesis feature of miR-34a transfected U251 cells was investigated and the expressions of CD31, CD34, Vwf, Notch 1, and Dll1 were quantified. Length of branching vessel-like structures in the miR-34a transfected U251 cells was significantly higher than control cells. The VEC feature of miR-34a overexpressed U251 cells was further confirmed by the expressions of CD31, CD34, and vWF. Transfection of miR-34a decreased the expression of Notch 1 and Dll1. Furthermore, the miR-34a overexpression-enhanced tube formation of GSCs was suppressed when the decreased expression of Dll1 was restored. The current study highlighted the potential of miR-34a as an inducer in GSCs' transdifferentiation into VECs by targeting Dll1.Entities:
Keywords: Notch 1; delta like 1; glioma stem cells; microRNA 34a; vascular endothelial cells
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Year: 2017 PMID: 28859546 DOI: 10.1080/09168451.2017.1364965
Source DB: PubMed Journal: Biosci Biotechnol Biochem ISSN: 0916-8451 Impact factor: 2.043