| Literature DB >> 27432276 |
Xing Su1, Xiaojiang Liu1, Lanchun Ni1, Wei Shi1, Hui Zhu1, Jinlong Shi1, Jian Chen1, Zhikai Gu1, Yilu Gao1, Qing Lan2, Qingfeng Huang1.
Abstract
Glioblastomas are understood to evolve from brain glioma stem cells (BGSCs), and yet the biology underlying this model of tumorigenesis is largely unknown. Paired box 3 protein (Pax3) is a member of the paired box (Pax) family of transcription factors that is normally expressed during embryonic development, but has recently been implicated in tumorigenesis. The present study demonstrated that Pax3 is differentially expressed in U87MG human glioma cell, BGSC and normal 1800 human astrocyte lines. Herein, we identified that the glial fibrillary acidic protein (GFAP), a major intermediate filament protein of mature astrocytes, is directly downregulated during the differentiation of BGSCs via the binding of Pax3 to the promoter region of GFAP. Moreover, siRNA silencing of Pax3 arrested BGSC differentiation, while overexpression of Pax3 promoted the differentiation in BGSCs. Furthermore, we studied the cell proliferation, invasion, apoptosis, differentiation and expression of Pax3 and GFAP in Pax3 siRNA-knockdown and Pax3-overexpressing BGSC models by CCK-8, Transwell migration, flow cytometry and western blot assays. The results indicate that Pax3 regulates GFAP expression, and that Pax3 may contribute to the evolution of BGSCs towards malignancy.Entities:
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Year: 2016 PMID: 27432276 DOI: 10.3892/or.2016.4917
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906