TY - JOUR
T1 - A genetic platform to model sarcomagenesis from primary adult mesenchymal stem cells
AU - Guarnerio, Jlenia
AU - Riccardi, Luisa
AU - Taulli, Riccardo
AU - Maeda, Takahiro
AU - Wang, Guocan
AU - Hobbs, Robin M.
AU - Song, Min Sup
AU - Sportoletti, Paolo
AU - Bernardi, Rosa
AU - Bronson, Roderick T.
AU - Castillo-Martin, Mireia
AU - Cordon-Cardo, Carlos
AU - Lunardi, Andrea
AU - Pandolfi, Pier Paolo
N1 - Publisher Copyright:
© 2015 American Association for Cancer Research.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - 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.
AB - 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.
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U2 - 10.1158/2159-8290.CD-14-1022
DO - 10.1158/2159-8290.CD-14-1022
M3 - Article
C2 - 25614485
AN - SCOPUS:84939502453
SN - 2159-8274
VL - 5
SP - 396
EP - 409
JO - Cancer Discovery
JF - Cancer Discovery
IS - 4
ER -