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Hepatocyte Growth Factor-mediated satellite cells niche perturbation promotes development of distinct sarcoma subtypes

Embryonal Rhabdomyosarcoma (ERMS) and Undifferentiated Pleomorphic Sarcoma (UPS) are distinct sarcoma subtypes. Here we investigate the relevance of the satellite cell (SC) niche in sarcoma development by using Hepatocyte Growth Factor (HGF) to perturb the niche microenvironment. In a Pax7 wild type...

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Detalles Bibliográficos
Autores principales: Morena, Deborah, Maestro, Nicola, Bersani, Francesca, Forni, Paolo Emanuele, Lingua, Marcello Francesco, Foglizzo, Valentina, Šćepanović, Petar, Miretti, Silvia, Morotti, Alessandro, Shern, Jack F, Khan, Javed, Ala, Ugo, Provero, Paolo, Sala, Valentina, Crepaldi, Tiziana, Gasparini, Patrizia, Casanova, Michela, Ferrari, Andrea, Sozzi, Gabriella, Chiarle, Roberto, Ponzetto, Carola, Taulli, Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811764/
https://www.ncbi.nlm.nih.gov/pubmed/26987019
http://dx.doi.org/10.7554/eLife.12116
Descripción
Sumario:Embryonal Rhabdomyosarcoma (ERMS) and Undifferentiated Pleomorphic Sarcoma (UPS) are distinct sarcoma subtypes. Here we investigate the relevance of the satellite cell (SC) niche in sarcoma development by using Hepatocyte Growth Factor (HGF) to perturb the niche microenvironment. In a Pax7 wild type background, HGF stimulation mainly causes ERMS that originate from satellite cells following a process of multistep progression. Conversely, in a Pax7 null genotype ERMS incidence drops, while UPS becomes the most frequent subtype. Murine EfRMS display genetic heterogeneity similar to their human counterpart. Altogether, our data demonstrate that selective perturbation of the SC niche results in distinct sarcoma subtypes in a Pax7 lineage-dependent manner, and define a critical role for the Met axis in sarcoma initiation. Finally, our results provide a rationale for the use of combination therapy, tailored on specific amplifications and activated signaling pathways, to minimize resistance emerging from sarcomas heterogeneity. DOI: http://dx.doi.org/10.7554/eLife.12116.001