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Status: Bibliographieeintrag

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Verfasst von:Creus-Bachiller, Edgar [VerfasserIn]   i
 Fernández-Rodríguez, Juana [VerfasserIn]   i
 Magallón-Lorenz, Miriam [VerfasserIn]   i
 Ortega-Bertran, Sara [VerfasserIn]   i
 Navas-Rutete, Susana [VerfasserIn]   i
 Romagosa, Cleofe [VerfasserIn]   i
 Silva, Tulio M. [VerfasserIn]   i
 Pané, Maria [VerfasserIn]   i
 Estival, Anna [VerfasserIn]   i
 Perez Sidelnikova, Diana [VerfasserIn]   i
 Morell, Mireia [VerfasserIn]   i
 Mazuelas, Helena [VerfasserIn]   i
 Carrió, Meritxell [VerfasserIn]   i
 Lausová, Tereza [VerfasserIn]   i
 Reuss, David [VerfasserIn]   i
 Gel, Bernat [VerfasserIn]   i
 Villanueva, Alberto [VerfasserIn]   i
 Serra, Eduard [VerfasserIn]   i
 Lázaro, Conxi [VerfasserIn]   i
Titel:Expanding a precision medicine platform for malignant peripheral nerve sheath tumors
Titelzusatz:new patient-derived orthotopic xenografts, cell lines and tumor entities
Verf.angabe:Edgar Creus-Bachiller, Juana Fernández-Rodríguez, Miriam Magallón-Lorenz, Sara Ortega-Bertran, Susana Navas-Rutete, Cleofe Romagosa, Tulio M. Silva, Maria Pané, Anna Estival, Diana Perez Sidelnikova, Mireia Morell, Helena Mazuelas, Meritxell Carrió, Tereza Lausová, David Reuss, Bernat Gel, Alberto Villanueva, Eduard Serra and Conxi Lázaro
E-Jahr:2023
Jahr:05 October 2023
Umfang:23 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 25.01.2024
Titel Quelle:Enthalten in: Molecular oncology
Ort Quelle:Hoboken, NJ : John Wiley & Sons, Inc., 2007
Jahr Quelle:2023
Band/Heft Quelle:(2023), online ahead of print
ISSN Quelle:1878-0261
Abstract:Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive soft-tissue sarcomas with a poor survival rate, presenting either sporadically or in the context of neurofibromatosis type 1 (NF1). The histological diagnosis of MPNSTs can be challenging, with different tumors exhibiting great histological and marker expression overlap. This heterogeneity could be partly responsible for the observed disparity in treatment response due to the inherent diversity of the preclinical models used. For several years, our group has been generating a large patient-derived orthotopic xenograft (PDOX) MPNST platform for identifying new precision medicine treatments. Herein, we describe the expansion of this platform using six primary tumors clinically diagnosed as MPNSTs, from which we obtained six additional PDOX mouse models and three cell lines, thus generating three pairs of in vitro-in vivo models. We extensively characterized these tumors and derived preclinical models, including genomic, epigenomic, and histological analyses. Tumors were reclassified after these analyses: three remained as MPNSTs (two being classic MPNSTs), one was a melanoma, another was a neurotrophic tyrosine receptor kinase (NTRK)-rearranged spindle cell neoplasm, and, finally, the last was an unclassifiable tumor bearing neurofibromin-2 (NF2) inactivation, a neuroblastoma RAS viral oncogene homolog (NRAS) oncogenic mutation, and a SWI/SNF-related matrix-associated actin-dependent regulator of chromatin (SMARCA4) heterozygous truncated variant. New cell lines and PDOXs faithfully recapitulated histology, marker expression, and genomic characteristics of the primary tumors. The diversity in tumor identity and their specific associated genomic alterations impacted treatment responses obtained when we used the new cell lines for testing compounds against known altered pathways in MPNSTs. In summary, we present here an extension of our MPNST precision medicine platform, with new PDOXs and cell lines, including tumor entities confounded as MPNSTs in a real clinical scenario. This platform may constitute a useful tool for obtaining correct preclinical information to guide MPNST clinical trials.
DOI:doi:10.1002/1878-0261.13534
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.1002/1878-0261.13534
 kostenfrei: Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/1878-0261.13534
 DOI: https://doi.org/10.1002/1878-0261.13534
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:cellular models
 MPNST
 NF1
 PDOX
 treatment response
 tumor entities
K10plus-PPN:1878994840
Verknüpfungen:→ Zeitschrift

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