CHD5 , a Tumor Suppressor Gene Deleted From 1p36.31 in Neuroblastomas

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CHD5, a Tumor Suppressor Gene Deleted From 1p36.31 in Neuroblastomas

BACKGROUND Neuroblastomas are characterized by hemizygous 1p deletions, suggesting that a tumor suppressor gene resides in this region. We previously mapped the smallest region of consistent deletion to a 2-Mb region of 1p36.31 that encodes 23 genes. Based on mutation analysis, expression pattern, and putative function, we identified CHD5 as the best tumor suppressor gene candidate. METHODS W...

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Novel CHD5, a tumor suppressor gene in neuroblastomas

Novel CHD5, a tumor suppressor gene in neuroblastomas Neuroblastoma, a tumor of the sympathetic nervous system, is the most common childhood extracranial solid tumor. The authors have identified different patterns of genetic change that underlie these disparate clinical behaviors. One of the most characteristic genetic changes in neuroblastomas is deletion of the short arm of hromosome 1 (1p). ...

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Role of microRNAs in epigenetic silencing of the CHD5 tumor suppressor gene in neuroblastomas

Neuroblastoma (NB), a tumor of the sympathetic nervous system, is the most common extracranial solid tumor of childhood. We and others have identified distinct patterns of genomic change that underlie diverse clinical behaviors, from spontaneous regression to relentless progression. We first identified CHD5 as a tumor suppressor gene that is frequently deleted in NBs. Mutation of the remaining ...

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Clusterin, a haploinsufficient tumor suppressor gene in neuroblastomas.

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Mechanisms of CHD5 Inactivation in neuroblastomas.

PURPOSE Neuroblastomas (NBs) have genomic, biological, and clinical heterogeneity. High-risk NBs are characterized by several genomic changes, including MYCN amplification and 1p36 deletion. We identified the chromatin-remodeling gene CHD5 as a tumor suppressor gene that maps to 1p36.31. Low or absent CHD5 expression is associated with a 1p36 deletion and an unfavorable outcome, but the mechani...

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ژورنال

عنوان ژورنال: JNCI: Journal of the National Cancer Institute

سال: 2008

ISSN: 0027-8874,1460-2105

DOI: 10.1093/jnci/djn176