Scientific Publications

Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy.

Publication TypeJournal Article
AuthorsBarretina, J., Taylor BS, Banerji S., Ramos AH, Lagos-Quintana M., Decarolis PL, Shah K., Socci ND, Weir BA, Ho A., Chiang DY, Reva B., Mermel CH, Getz G., Antipin Y., Beroukhim R., Major JE, Hatton C., Nicoletti R., Hanna M., Sharpe T., Fennell TJ, Cibulskis K., Onofrio RC, Saito T., Shukla N., Lau C., Nelander S., Silver SJ, Sougnez C., Viale A., Winckler W., Maki RG, Garraway LA, Lash A., Greulich H., Root DE, Sellers WR, Schwartz GK, Antonescu CR, Lander E. S., Varmus HE, Ladanyi M., Sander C., Meyerson M., and Singer S.
AbstractSoft-tissue sarcomas, which result in approximately 10,700 diagnoses and 3,800 deaths per year in the United States, show remarkable histologic diversity, with more than 50 recognized subtypes. However, knowledge of their genomic alterations is limited. We describe an integrative analysis of DNA sequence, copy number and mRNA expression in 207 samples encompassing seven major subtypes. Frequently mutated genes included TP53 (17% of pleomorphic liposarcomas), NF1 (10.5% of myxofibrosarcomas and 8% of pleomorphic liposarcomas) and PIK3CA (18% of myxoid/round-cell liposarcomas, or MRCs). PIK3CA mutations in MRCs were associated with Akt activation and poor clinical outcomes. In myxofibrosarcomas and pleomorphic liposarcomas, we found both point mutations and genomic deletions affecting the tumor suppressor NF1. Finally, we found that short hairpin RNA (shRNA)-based knockdown of several genes amplified in dedifferentiated liposarcoma, including CDK4 and YEATS4, decreased cell proliferation. Our study yields a detailed map of molecular alterations across diverse sarcoma subtypes and suggests potential subtype-specific targets for therapy.
Year of Publication2010
JournalNature genetics
Volume42
Issue8
Pages715-21
Date Published (YYYY/MM/DD)2010/08/01
ISSN Number1061-4036
DOI10.1038/ng.619
PubMedhttp://www.ncbi.nlm.nih.gov/pubmed/20601955?dopt=Abstract