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Pax3 loss of function delays tumour progression in kRAS-induced zebrafish rhabdomyosarcoma models.
Kahsay, A; Rodriguez-Marquez, E; López-Pérez, A; Hörnblad, A; von Hofsten, J.
Afiliación
  • Kahsay A; Integrative Medical Biology (IMB), Umeå University, Johan Bures Väg 12, 90187, Umeå, Sweden.
  • Rodriguez-Marquez E; Integrative Medical Biology (IMB), Umeå University, Johan Bures Väg 12, 90187, Umeå, Sweden.
  • López-Pérez A; Umeå Centre for Molecular Medicine (UCMM), Umeå University, Johan Bures Väg 12, 90187, Umeå, Sweden.
  • Hörnblad A; Umeå Centre for Molecular Medicine (UCMM), Umeå University, Johan Bures Väg 12, 90187, Umeå, Sweden.
  • von Hofsten J; Integrative Medical Biology (IMB), Umeå University, Johan Bures Väg 12, 90187, Umeå, Sweden. jonas.von.hofsten@umu.se.
Sci Rep ; 12(1): 17149, 2022 10 13.
Article en En | MEDLINE | ID: mdl-36229514
ABSTRACT
Rhabdomyosarcoma is a soft tissue cancer that arises in skeletal muscle due to mutations in myogenic progenitors that lead to ineffective differentiation and malignant transformation. The transcription factors Pax3 and Pax7 and their downstream target genes are tightly linked with the fusion positive alveolar subtype, whereas the RAS pathway is usually involved in the embryonal, fusion negative variant. Here, we analyse the role of Pax3 in a fusion negative context, by linking alterations in gene expression in pax3a/pax3b double mutant zebrafish with tumour progression in kRAS-induced rhabdomyosarcoma tumours. Several genes in the RAS/MAPK signalling pathway were significantly down-regulated in pax3a/pax3b double mutant zebrafish. Progression of rhabdomyosarcoma tumours was also delayed in the pax3a/pax3b double mutant zebrafish indicating that Pax3 transcription factors have an unappreciated role in mediating malignancy in fusion negative rhabdomyosarcoma.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Rabdomiosarcoma / Rabdomiosarcoma Embrionario Tipo de estudio: Prognostic_studies Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Rabdomiosarcoma / Rabdomiosarcoma Embrionario Tipo de estudio: Prognostic_studies Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article