Integrated molecular characterization of chondrosarcoma reveals critical determinants of disease progression

被引:61
|
作者
Nicolle, Remy [1 ]
Ayadi, Mira [1 ]
Gomez-Brouchet, Anne [2 ]
Armenoult, Lucile [1 ]
Banneau, Guillaume [1 ]
Elarouci, Nabila [1 ]
Tallegas, Matthias [3 ]
Decouvelaere, Anne-Valerie [4 ,5 ]
Aubert, Sebastien [6 ]
Redini, Francoise [7 ]
Marie, Beatrice [8 ]
Labit-Bouvier, Corinne [9 ]
Reina, Nicolas [10 ]
Karanian, Marie [4 ,5 ]
Le Nail, Louis-Romee [7 ,11 ]
Anract, Philippe [12 ]
Gouin, Francois [13 ,14 ]
Larousserie, Frederique [15 ]
de Reynies, Aurelien [1 ]
de Pinieux, Gonzague [7 ,16 ]
机构
[1] Ligue Natl Canc, Programme Cartes Identite Tumeurs CIT, Paris, France
[2] Univ Toulouse, Dept Pathol, CHU Toulouse Oncopole, Toulouse, France
[3] CHRU Tours, Plateforme Genet Mol Canc, Tours, France
[4] Ctr Leon Berard, Dept Biopathol, Lyon, France
[5] Univ Claude Bernard Lyon 1, Univ Lyon, CNRS 5286, Canc Res Ctr Lyon,INSERM U1052, Lyon, France
[6] Univ Lille, Dept Pathol, CHU Lille, Lille, France
[7] Univ Nantes, UMR1238, INSERM, Sarcomes Osseux & Remodelage Tissus Calcifies,Fac, Nantes, France
[8] CHU Nancy, Dept Pathol, Nancy, France
[9] Aix Marseille Univ, CHU Marseille, Dept Pathol, INSERM,MMG, Marseille, France
[10] CHU Toulouse, Dept Orthoped Surg, Hop Pierre Paul Riquet, Toulouse, France
[11] Univ Tours, Dept Orthoped Surg, CHRU Tours, Tours, France
[12] Univ Paris 05, Sorbonne Paris Cite, Hop Cochin, AP HP,Dept Orthoped Surg, Paris, France
[13] Ctr Leon Berard, Dept Surg, Lyon, France
[14] CHU Nantes, Dept Orthopaed Surg, Nantes, France
[15] Univ Paris 05, Hop Cochin, AP HP, Serv Pathol, Paris, France
[16] Univ Tours, Dept Pathol, CHRU Tours, Tours, France
关键词
EXPRESSION; MUTATIONS;
D O I
10.1038/s41467-019-12525-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chondrosarcomas are primary cancers of cartilaginous tissue with highly contrasting prognoses. These tumors are defined by recurrent mutations in the IDH genes and other genetic alterations including inactivation of CDKN2A and COL2A1; however, these have no clinical value. Here we use multi-omics molecular profiles from a series of cartilage tumors and find an mRNA classification that identifies two subtypes of chondrosarcomas defined by a balance in tumor differentiation and cell cycle activation. The microRNA classification reveals the importance of the loss of expression of the 14q32 locus in defining the level of malignancy. Finally, DNA methylation is associated with IDH mutations. We can use the multi-omics classifications to predict outcome. We propose an mRNA-only classifier to reproduce the integrated multi-omics classification, and its application to relapsed tumor samples shows the progressive nature of the classification. Thus, it may be possible to use mRNA-based signatures to detect patients with high-risk chondrosarcomas.
引用
收藏
页数:11
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