Synthetic MIR143-3p Suppresses Cell Growth in Rhabdomyosarcoma Cells by Interrupting RAS Pathways Including PAX3–FOXO1

SIMPLE SUMMARY: Rhabdomyosarcoma (RMS) is a soft tissue sarcoma with embryonal (ERMS) and alveoral (ARMS) features, most frequently found in children. ARMS has the worse prognosis due to the formation of the chimeric PAX3–FOXO1 gene. New therapies are needed for the treatment of ARMS. The aim of thi...

Descripción completa

Detalles Bibliográficos
Autores principales: Sugito, Nobuhiko, Heishima, Kazuki, Ito, Yuko, Akao, Yukihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696565/
https://www.ncbi.nlm.nih.gov/pubmed/33182548
http://dx.doi.org/10.3390/cancers12113312

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696565/
https://www.ncbi.nlm.nih.gov/pubmed/33182548
http://dx.doi.org/10.3390/cancers12113312

Ejemplares similares