| Literature DB >> 25614485 |
Jlenia Guarnerio1, Luisa Riccardi1, Riccardo Taulli1, Takahiro Maeda2, Guocan Wang1, Robin M Hobbs1, Min Sup Song1, Paolo Sportoletti1, Rosa Bernardi3, Roderick T Bronson4, Mireia Castillo-Martin5, Carlos Cordon-Cardo5, Andrea Lunardi6, Pier Paolo Pandolfi6.
Abstract
UNLABELLED: The regulatory factors governing adult mesenchymal stem cell (MSC) physiology and their tumorigenic potential are still largely unknown, which substantially delays the identification of effective therapeutic approaches for the treatment of aggressive and lethal forms of MSC-derived mesenchymal tumors, such as undifferentiated sarcomas. Here, we have developed a novel platform to screen and quickly identify genes and pathways responsible for adult MSC transformation, modeled undifferentiated sarcoma in vivo, and, ultimately, tested the efficacy of targeting the identified oncopathways. Importantly, by taking advantage of this new platform, we demonstrate the key role of an aberrant LRF-DLK1-SOX9 pathway in the pathogenesis of undifferentiated sarcoma, with important therapeutic implications. SIGNIFICANCE: The paucity of therapeutic options for the treatment of sarcoma calls for a rapid and effective preclinical assessment of new therapeutic modalities. We have here developed a new platform to deconstruct the molecular genetics underlying the pathogenesis of sarcoma and to evaluate in vivo the efficacy of novel targeted therapies. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 25614485 PMCID: PMC4418175 DOI: 10.1158/2159-8290.CD-14-1022
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397