Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma

Andrew Futreal and colleagues identify the major cartilage collagen gene COL2A1 as a frequent target of somatic mutation in chondrosarcoma. The mutation patterns are consistent with selection for variants likely to impair normal collagen biosynthesis. Chondrosarcoma is a heterogeneous collection of...

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Veröffentlicht in:Nature genetics 2013-08, Vol.45 (8), p.923-926
Hauptverfasser: Tarpey, Patrick S, Behjati, Sam, Cooke, Susanna L, Van Loo, Peter, Wedge, David C, Pillay, Nischalan, Marshall, John, O'Meara, Sarah, Davies, Helen, Nik-Zainal, Serena, Beare, David, Butler, Adam, Gamble, John, Hardy, Claire, Hinton, Jonathon, Jia, Ming Ming, Jayakumar, Alagu, Jones, David, Latimer, Calli, Maddison, Mark, Martin, Sancha, McLaren, Stuart, Menzies, Andrew, Mudie, Laura, Raine, Keiran, Teague, Jon W, Tubio, Jose M C, Halai, Dina, Tirabosco, Roberto, Amary, Fernanda, Campbell, Peter J, Stratton, Michael R, Flanagan, Adrienne M, Futreal, P Andrew
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Sprache:eng
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Zusammenfassung:Andrew Futreal and colleagues identify the major cartilage collagen gene COL2A1 as a frequent target of somatic mutation in chondrosarcoma. The mutation patterns are consistent with selection for variants likely to impair normal collagen biosynthesis. Chondrosarcoma is a heterogeneous collection of malignant bone tumors and is the second most common primary malignancy of bone after osteosarcoma. Recent work has identified frequent, recurrent mutations in IDH1 or IDH2 in nearly half of central chondrosarcomas. However, there has been little systematic genomic analysis of this tumor type, and, thus, the contribution of other genes is unclear. Here we report comprehensive genomic analyses of 49 individuals with chondrosarcoma (cases). We identified hypermutability of the major cartilage collagen gene COL2A1 , with insertions, deletions and rearrangements identified in 37% of cases. The patterns of mutation were consistent with selection for variants likely to impair normal collagen biosynthesis. In addition, we identified mutations in IDH1 or IDH2 (59%), TP53 (20%), the RB1 pathway (33%) and Hedgehog signaling (18%).
ISSN:1061-4036
1546-1718
DOI:10.1038/ng.2668