| Literature DB >> 12209999 |
Naoki Yokota1, Shigeru Nishizawa, Seiji Ohta, Hiroaki Date, Haruhiko Sugimura, Hiroki Namba, Masato Maekawa.
Abstract
To clarify the roles of Wnt pathway in medulloblastoma oncogenesis, immunohistochemical staining of beta-catenin and Wnt-1 and genomic analyses of CTNNB1 (beta-catenin) and AXIN1 (axin 1) were examined in 23 sporadic cases. Accumulation of beta-catenin in tumor cells was immunohistochemically proven in 5 cases; 2 cases showed positive immunoreactivity for Wnt-1 and another 2 showed mutation of either CTNNB1 or AXIN1. AXIN1 mutation was in exon 3, corresponding to GSK-3beta 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 beta-catenin, followed by cell proliferation and medulloblastoma oncogenesis. Copyright 2002 Wiley-Liss, Inc.Entities:
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Year: 2002 PMID: 12209999 DOI: 10.1002/ijc.10559
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396