Sonic hedgehog and insulin-like growth factor signaling synergize to induce medulloblastoma formation from nestin-expressing neural progenitors in mice

被引:185
作者
Rao, G
Pedone, CA
Del Valle, L
Reiss, K
Holland, EC
Fults, DW
机构
[1] Univ Utah, Sch Med, Dept Neurosurg, Salt Lake City, UT 84132 USA
[2] Temple Univ, Ctr Neurovirol & Canc Biol, Philadelphia, PA 19112 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Surg Neurosurg, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Neurol & Cell Biol, New York, NY 10021 USA
关键词
medulloblastoma; IGF2; sonic hedgehog; RCAS/tv-a; neural progenitors;
D O I
10.1038/sj.onc.1207818
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Medulloblastoma (MB) is a malignant brain tumor that arises in the cerebellum of children. Activation of the Sonic hedgehog/Patched (Shh/Ptc) signaling pathway in neural progenitor cells of the cerebellum induces MBs in mice. The incomplete penetrance of tumor formation in mice, coupled with the low frequency of mutations in Shh/Ptc pathway genes in human tumors, suggests that other signaling molecules cooperate with Shh to enhance MB formation. We modeled the ability of insulin-like growth factor (IGF) signaling to induce MB using the RCAS/tv-a system, which allows postnatal gene transfer and expression in a cell-type-specific manner. We used RCAS retroviral vectors to target expression of Shh, IGF2, and activated Akt to nestin-expressing neural progenitors in the cerebella of newborn mice. The incidence of Shh-induced tumor formation (15%) was enhanced by coexpression with IGF2 (39%) and Akt (48%). Neither IGF2 nor Akt caused tumors when expressed independently. The induced tumors showed upregulated expression of insulin receptor substrate 1 and phosphorylated forms of IGF1 receptor and Akt, mimicking activated IGF signaling found in human MBs. These results indicate that combined activation of the Shh/Ptc and IGF signaling pathways is an important mechanism in MB pathogenesis.
引用
收藏
页码:6156 / 6162
页数:7
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