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CASZ1, a candidate tumor-suppressor gene, suppresses neuroblastoma tumor growth through reprogramming gene expression

Neuroblastoma (NB) is a common childhood malignant tumor of the neural crest-derived sympathetic nervous system. In NB the frequent loss of heterozygosity (LOH) on chromosome 1p raises the possibility that this region contains tumor-suppressor genes whose inactivation contributes to tumorigenesis. T...

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Bibliographic Details
Published in:Cell death and differentiation 2011-07, Vol.18 (7), p.1174-1183
Main Authors: Liu, Z, Yang, X, Li, Z, McMahon, C, Sizer, C, Barenboim-Stapleton, L, Bliskovsky, V, Mock, B, Ried, T, London, W B, Maris, J, Khan, J, Thiele, C J
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Language:English
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Summary:Neuroblastoma (NB) is a common childhood malignant tumor of the neural crest-derived sympathetic nervous system. In NB the frequent loss of heterozygosity (LOH) on chromosome 1p raises the possibility that this region contains tumor-suppressor genes whose inactivation contributes to tumorigenesis. The human homolog of the Drosophila neural fate determination gene CASZ1, a zinc-finger transcription factor, maps to chromosome 1p36.22, a region implicated in NB tumorigenesis. Quantitative real-time PCR analysis showed that low- CASZ1 expression is significantly correlated with increased age (≥18 months), Children's Oncology Group high-risk classification, 1p LOH and MYCN amplification (all P
ISSN:1350-9047
1476-5403
DOI:10.1038/cdd.2010.187