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Activation of Sonic hedgehog signaling in neural progenitor cells promotes glioma development in the zebrafish optic pathway

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Title Activation of Sonic hedgehog signaling in neural progenitor cells promotes glioma development in the zebrafish optic pathway
Names Ju, B. (creator)
Chen, W. (creator)
Spitsbergen, J. M. (creator)
et al. (creator)
Date Issued 2014-03-31 (iso8601)
Note This is the publisher’s final pdf. The published article is copyrighted by the author(s) and published by the Nature Publishing Group. The published article can be found at: http://www.nature.com/oncsis/index.html.
Abstract Dysregulation of Sonic hedgehog (Shh) signaling has been implicated in glioma pathogenesis. Yet, the role of this pathway
in gliomagenesis remains controversial because of the lack of relevant animal models. Using the cytokeratin 5 promoter, we
ectopically expressed a constitutively active zebrafish Smoothened (Smoa1) in neural progenitor cells and analyzed tumorigenic
capacity of activated Shh signaling in both transient and stable transgenic fish. Transient transgenic fish overexpressing Smoa1
developed retinal and brain tumors, suggesting smoa1 is oncogenic in the zebrafish central nervous system (CNS). We further
established stable transgenic lines that simultaneously developed optic pathway glioma (OPG) and various retinal tumors. In one
of these lines, up to 80% of F1 and F2 fish developed tumors within 1 year of age. Microarray analysis of tumor samples showed
upregulated expression of genes involved in the cell cycle, cancer signaling and Shh downstream targets ptc1, gli1 and gli2a.
Tumors also exhibited specific gene signatures characteristic of radial glia and progenitor cells as transcriptions of radial glia genes
cyp19a1b, s100β, blbp, gfap and the stem/progenitor genes nestin and sox2 were significantly upregulated. Overexpression of GFAP,
S100β, BLBP and Sox2 was confirmed by immunofluorescence. We also detected overexpression of Mdm2 throughout the optic
pathway in fish with OPG, therefore implicating the Mdm2–Tp53 pathway in glioma pathogenesis. In conclusion, we demonstrate
that activated Shh signaling initiates tumorigenesis in the zebrafish CNS and provide the first OPG model not associated with
neurofibromatosis 1.
Genre Article
Access Condition http://creativecommons.org/licenses/by-nc-sa/3.0/us/
Topic Zebrafish
Identifier Ju, B., Chen, W., Spitsbergen, J. M., Lu, J., Vogel, P., Peters, J. L., ... & Taylor, M. R. (2014). Activation of Sonic hedgehog signaling in neural progenitor cells promotes glioma development in the zebrafish optic pathway. Oncogenesis, 3, e96. doi:10.1038/oncsis.2014.10

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