Abstract B35: Liaison between SNAI2 and MYOD enhances oncogenesis and suppresses differentiation in fusion-negative rhabdomyosarcoma

Rhabdomyosarcoma (RMS) is a pediatric malignancy of the muscle, and patients with high-risk fusion-negative RMS (FN-RMS), the major subtype of this disease, are associated with RAS pathway activating mutations and have a poor survival rate of

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2020-07, Vol.80 (14_Supplement), p.B35-B35
Hauptverfasser: Pomella, Silvia, Sreenivas, Prethish, Gryder, Berkley E., Wang, Long, Cassandri, Matteo, Baxi, Kunal, Hensch, Nicole R., Carcarino, Elena, Song, Young, Yohe, Marielle, Amadio, Bruno, Caruana, Ignazio, De Stefanis, Cristiano, De Vito, Rita, Locatelli, Franco, Chen, Yidong, Chen, Eleanor Y., Houghton, Peter, Khan, Javed, Rota, Rossella, Ignatius, Myron S.
Format: Artikel
Sprache:eng
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Zusammenfassung:Rhabdomyosarcoma (RMS) is a pediatric malignancy of the muscle, and patients with high-risk fusion-negative RMS (FN-RMS), the major subtype of this disease, are associated with RAS pathway activating mutations and have a poor survival rate of
ISSN:0008-5472
1538-7445
DOI:10.1158/1538-7445.PEDCA19-B35