Dedifferentiation of Neurons and Astrocytes by Oncogenes Can Induce Gliomas in Mice

被引:411
作者
Friedmann-Morvinski, Dinorah [1 ]
Bushong, Eric A. [2 ]
Ke, Eugene [1 ,3 ]
Soda, Yasushi [1 ]
Marumoto, Tomotoshi [1 ,4 ]
Singer, Oded [1 ]
Ellisman, Mark H. [2 ]
Verma, Inder M. [1 ]
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Natl Ctr Microscopy & Imaging Res, Ctr Res Biol Syst, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Grad Program Bioinformat, La Jolla, CA 92093 USA
[4] Kyushu Univ, Dept Mol Genet, Div Mol & Clin Genet, Med Inst Bioregulat,Higashi Ku, Fukuoka 8128582, Japan
基金
美国国家卫生研究院;
关键词
NEURAL STEM-CELLS; MOUSE MODELS; BRAIN; GLIOBLASTOMA; ORIGIN; NF1; NEUROGENESIS; PROGRESSION; EXPRESSION; DISEASE;
D O I
10.1126/science.1226929
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Glioblastoma multiforme (GBM) is the most common and aggressive malignant primary brain tumor in humans. Here we show that gliomas can originate from differentiated cells in the central nervous system (CNS), including cortical neurons. Transduction by oncogenic lentiviral vectors of neural stem cells (NSCs), astrocytes, or even mature neurons in the brains of mice can give rise to malignant gliomas. All the tumors, irrespective of the site of lentiviral vector injection (the initiating population), shared common features of high expression of stem or progenitor markers and low expression of differentiation markers. Microarray analysis revealed that tumors of astrocytic and neuronal origin match the mesenchymal GBM subtype. We propose that most differentiated cells in the CNS upon defined genetic alterations undergo dedifferentiation to generate a NSC or progenitor state to initiate and maintain the tumor progression, as well as to give rise to the heterogeneous populations observed in malignant gliomas.
引用
收藏
页码:1080 / 1084
页数:5
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