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Penelope DeCarolis
Researcher at Memorial Sloan Kettering Cancer Center
Publications - 15
Citations - 1578
Penelope DeCarolis is an academic researcher from Memorial Sloan Kettering Cancer Center. The author has contributed to research in topics: Liposarcoma & Cellular differentiation. The author has an hindex of 14, co-authored 15 publications receiving 1439 citations.
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Journal ArticleDOI
Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy.
Jordi Barretina,Barry S. Taylor,Barry S. Taylor,Shantanu Banerji,Shantanu Banerji,Alexis Ramos,Alexis Ramos,Mariana Lagos-Quintana,Penelope DeCarolis,Kinjal Shah,Kinjal Shah,Nicholas D. Socci,Barbara A. Weir,Barbara A. Weir,Alan L. Ho,Derek Y. Chiang,Derek Y. Chiang,Boris Reva,Craig H. Mermel,Craig H. Mermel,Gad Getz,Yevgeniy Antipin,Rameen Beroukhim,Rameen Beroukhim,John E. Major,Charlie Hatton,Richard Nicoletti,Megan Hanna,Ted Sharpe,Timothy Fennell,Kristian Cibulskis,Robert C. Onofrio,Tsuyoshi Saito,Neerav Shukla,Christopher Lau,Sven Nelander,Serena J. Silver,Carrie Sougnez,Agnes Viale,Wendy Winckler,Wendy Winckler,Robert G. Maki,Levi A. Garraway,Levi A. Garraway,Alex E. Lash,Heidi Greulich,Heidi Greulich,David E. Root,William R. Sellers,Gary K. Schwartz,Cristina R. Antonescu,Eric S. Lander,Harold E. Varmus,Marc Ladanyi,Chris Sander,Matthew Meyerson,Samuel Singer +56 more
TL;DR: An integrative analysis of DNA sequence, copy number and mRNA expression in 207 samples encompassing seven major subtypes of soft-tissue sarcomas yields a detailed map of molecular alterations across diverse sarcoma subtypes and suggests potential subtype-specific targets for therapy.
Journal ArticleDOI
Gene expression profiling of liposarcoma identifies distinct biological types/subtypes and potential therapeutic targets in well-differentiated and dedifferentiated liposarcoma.
Samuel Singer,Nicholas D. Socci,Grazia Ambrosini,Elliot B. Sambol,Penelope DeCarolis,Yuhsin Wu,Rachael O'Connor,Robert G. Maki,Agnes Viale,Chris Sander,Gary K. Schwartz,Cristina R. Antonescu +11 more
TL;DR: It is shown that Nutlin-3a, an antagonist of MDM2, preferentially induces apoptosis and growth arrest in dedifferentiated liposarcoma cells compared with normal adipocytes, and the promise of using this expression dataset for new drug discovery in liposARcoma is shown.
Journal ArticleDOI
Functional Copy-Number Alterations in Cancer
Barry S. Taylor,Jordi Barretina,Jordi Barretina,Nicholas D. Socci,Penelope DeCarolis,Marc Ladanyi,Matthew Meyerson,Matthew Meyerson,Samuel Singer,Chris Sander +9 more
TL;DR: A comprehensive computational approach to robustly map chromosomal alterations in tumor samples and assess their functional importance in cancer is presented, applicable to high-resolution genomic data.
Journal ArticleDOI
Small RNA sequencing and functional characterization reveals microRNA-143 tumor suppressor activity in liposarcoma
Stacy Ugras,Elliott R. Brill,Anders Jacobsen,Markus Hafner,Nicholas D. Socci,Penelope DeCarolis,Raya Khanin,Rachael O'Connor,Aleksandra Mihailovic,Barry S. Taylor,Robert L. Sheridan,Jeffrey M. Gimble,Agnes Viale,Aimee M. Crago,Cristina R. Antonescu,Chris Sander,Thomas Tuschl,Samuel Singer +17 more
TL;DR: Re-expression vectors or selective agents directed at miR-143 or its targets may have therapeutic value in dedifferentiated liposarcoma, and treatment with a PLK1 inhibitor potently induced G(2)-M growth arrest and apoptosis in liposARcoma cells.
Journal ArticleDOI
Frequent Alterations and Epigenetic Silencing of Differentiation Pathway Genes in Structurally Rearranged Liposarcomas
Barry S. Taylor,Penelope DeCarolis,Christina V. Angeles,Fabienne Brenet,Nikolaus Schultz,Cristina R. Antonescu,Joseph M. Scandura,Chris Sander,Agnes Viale,Nicholas D. Socci,Samuel Singer +10 more
TL;DR: Multimodality sequence analysis of DLPS revealed recurrent mutations and epigenetic abnormalities critical to liposarcomagenesis and to the suppression of adipocyte differentiation, revealing an unanticipated role for methylation abnormalities in DLPS tumors and suggesting demethylating agents as potential therapeutics.