| Literature DB >> 34156092 |
Robert Tyler1, Mark P Dilworth1, Jonathan James1, Daniel Blakeway1, Joanne D Stockton1, Dion G Morton1, Phillipe Taniere2, David Gourevitch2, Anant Desai2, Andrew D Beggs1.
Abstract
Well differentiated liposarcoma (WD-LPS) is a relatively rare tumour, with fewer than 50 cases occurring per year in the UK. These tumours are both chemotherapy- and radiotherapy-resistant and present a significant treatment challenge requiring radical surgery. Little is known of the molecular landscape of these tumours and no current targets for molecular therapy exist. We aimed to carry out a comprehensive molecular characterisation of WD-LPS via whole genome sequencing, RNA sequencing, and methylation array analysis. A recurrent mutation within exon 1 of FOXD4L3 was observed (chr9:70,918,189A>T; c.322A>T; p.Lys108Ter). Recurrent mutations were also observed in Wnt signalling, immunity, DNA repair, and hypoxia-associated genes. Recurrent amplification of HGMA2 was observed, although this was in fact part of a general amplification of the region around this gene. Recurrent gene fusions in HGMA2, SDHA, TSPAN31, and MDM2 were also observed as well as consistent rearrangements between chromosome 6 and chromosome 12. Our study has demonstrated a recurrent mutation within FOXD4L3, which shows evidence of interaction with the PAX pathway to promote tumourigenesis.Entities:
Keywords: RNA sequencing; liposarcoma; methylation; whole genome sequencing
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Year: 2021 PMID: 34156092 DOI: 10.1002/path.5749
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996