| Literature DB >> 19373855 |
Tim Forshew1, Ruth G Tatevossian, Andrew R J Lawson, Jing Ma, Geoff Neale, Babatunji W Ogunkolade, Tania A Jones, Johan Aarum, James Dalton, Simon Bailey, Tracy Chaplin, Rowena L Carter, Amar Gajjar, Alberto Broniscer, Bryan D Young, David W Ellison, Denise Sheer.
Abstract
We report genetic aberrations that activate the ERK/MAP kinase pathway in 100% of posterior fossa pilocytic astrocytomas, with a high frequency of gene fusions between KIAA1549 and BRAF among these tumours. These fusions were identified from analysis of focal copy number gains at 7q34, detected using Affymetrix 250K and 6.0 SNP arrays. PCR and sequencing confirmed the presence of five KIAA1549-BRAF fusion variants, along with a single fusion between SRGAP3 and RAF1. The resulting fusion genes lack the auto-inhibitory domains of BRAF and RAF1, which are replaced in-frame by the beginning of KIAA1549 and SRGAP3, respectively, conferring constitutive kinase activity. An activating mutation of KRAS was identified in the single pilocytic astrocytoma without a BRAF or RAF1 fusion. Further fusions and activating mutations in BRAF were identified in 28% of grade II astrocytomas, highlighting the importance of the ERK/MAP kinase pathway in the development of paediatric low-grade gliomas.Entities:
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Year: 2009 PMID: 19373855 DOI: 10.1002/path.2558
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996