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

Rhabdomyosarcoma (RMS) is a soft tissue sarcoma most frequently found in children. In RMS, there are two major subtypes, embryonal RMS (ERMS) and alveolar RMS (ARMS). ARMS has the worse prognosis of the two owing to the formation of the chimeric <i>PAX3–FOXO1</i> gene. A novel therapeuti...

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Bibliographic Details
Main Authors: Nobuhiko Sugito, Kazuki Heishima, Yuko Ito, Yukihiro Akao
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Cancers
Subjects:
RMS
Online Access:https://www.mdpi.com/2072-6694/12/11/3312