To clarify the roles of Wnt pathway in medulloblastoma oncogenesis, immunohistochemical staining of β-catenin and Wnt-1 and genomic analyses of CTNNB1 (β-catenin) and AXIN1 (axin 1) were examined in 23 sporadic cases. Accumulation of β-catenin in tumor cells was immunohistochemically proven in 5 cases; 2 cases showed positive immunore-activity for Wnt-1 and another 2 showed mutation of either CTNNB1 or AXIN1. AXIN1 mutation was in exon 3, corresponding to GSK-3β binding site and CTNNB1 mutation was in exon 3, corresponding to its phosphorylation site. Disruption of these proteins could result in upregulation of the Wnt signaling and accumulation of β-catenin, followed by cell proliferation and medulloblastoma oncogenesis. © 2002 Wiley-Liss, Inc.
CITATION STYLE
Yokota, N., Nishizawa, S., Ohta, S., Date, H., Sugimura, H., Namba, H., & Maekawa, M. (2002). Role of Wnt pathway in medulloblastoma oncogenesis. International Journal of Cancer, 101(2), 198–201. https://doi.org/10.1002/ijc.10559
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