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Oncogene. 2010 Nov 18;29(46):6138-48. doi: 10.1038/onc.2010.342. Epub 2010 Aug 16.

The CASPR2 cell adhesion molecule functions as a tumor suppressor gene in glioma.

Author information

1
Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.

Abstract

Genomic translocations have been implicated in cancer. In this study, we performed a screen for genetic translocations in gliomas based on exon-level expression profiles. We identified a translocation in the contactin-associated protein-like 2 (CASPR2) gene, encoding a cell adhesion molecule. CASPR2 mRNA was fused to an expressed sequence tag that likely is part of the nuclear receptor coactivator 1 gene. Despite high mRNA expression levels, no CASPR2 fusion protein was detected. In a set of 25 glioblastomas and 22 oligodendrogliomas, mutation analysis identified two additional samples with genetic alterations in the CASPR2 gene and all three identified genetic alterations are likely to reduce CASPR2 protein expression levels. Methylation of the CASPR2 gene was also observed in gliomas and glioma cell lines. CASPR2-overexpressing cells showed decreased proliferation rates, likely because of an increase in apoptosis. Moreover, high CASPR2 mRNA expression level is positively correlated with survival and is an independent prognostic factor. These results indicate that CASPR2 acts as a tumor suppressor gene in glioma.

PMID:
20711234
DOI:
10.1038/onc.2010.342
[Indexed for MEDLINE]

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