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靶向N-CoR通路可诱导胶质母细胞瘤来源的癌症干细胞分化。

N-CoR pathway targeting induces glioblastoma derived cancer stem cell differentiation.

作者信息

Park Deric M, Li Jie, Okamoto Hiroaki, Akeju Oluwaseun, Kim Stephanie H, Lubensky Irina, Vortmeyer Alexander, Dambrosia James, Weil Robert J, Oldfield Edward H, Park John K, Zhuang Zhengping

机构信息

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Cell Cycle. 2007 Feb 15;6(4):467-70. doi: 10.4161/cc.6.4.3856. Epub 2007 Feb 12.

Abstract

Nuclear receptor corepressor (N-CoR) is a critical regulator of neural stem cell differentiation. Nuclear localization of N-CoR is a feature of undifferentiated neural stem cells and cytoplasmic translocation of N-CoR leads to astrocytic differentiation. Comparative proteomic analysis of microdissected glioblastoma multiforme (GBM) specimens and matched normal glial tissue reveals increased expression of N-CoR in GBM. In GBM primary cell cultures, tumor cells with nuclear localization of N-CoR demonstrate an undifferentiated phenotype, but are subject to astroglial differentiation upon exposure to agents promoting phosphorylation of N-CoR and its subsequent translocation to the cytoplasm. Treatment of glioma cell lines with a combination of retinoic acid and low-dose okadaic acid decreases the corepressor effect of N-CoR and has a striking synergistic effect on growth inhibition. The identification of N-CoR in GBM provides insights into the tumorigenesis process and supports the development of differentiation-based therapeutic strategies.

摘要

核受体共抑制因子(N-CoR)是神经干细胞分化的关键调节因子。N-CoR的核定位是未分化神经干细胞的一个特征,而N-CoR的细胞质转位会导致星形胶质细胞分化。对显微切割的多形性胶质母细胞瘤(GBM)标本和匹配的正常神经胶质组织进行的比较蛋白质组学分析显示,GBM中N-CoR的表达增加。在GBM原代细胞培养中,N-CoR核定位的肿瘤细胞表现出未分化表型,但在暴露于促进N-CoR磷酸化及其随后转位至细胞质的试剂后会发生星形胶质细胞分化。用视黄酸和低剂量冈田酸联合处理胶质瘤细胞系可降低N-CoR的共抑制作用,并对生长抑制具有显著的协同作用。在GBM中鉴定出N-CoR为肿瘤发生过程提供了见解,并支持基于分化的治疗策略的开发。

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