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Combination of HDAC and FYN inhibitors in synovial sarcoma treatment.
Parker, Kyra; Zhang, Yanfeng; Anchondo, Gavin; Smith, Ashlyn; Guerrero Pacheco, Sergio; Kondo, Tadashi; Su, Le.
Afiliación
  • Parker K; Department of Biology, Jacksonville State University, Jacksonville, AL, United States.
  • Zhang Y; Department of Genetics, The University of Alabama at Birmingham, Birmingham, AL, United States.
  • Anchondo G; Department of Biology, Jacksonville State University, Jacksonville, AL, United States.
  • Smith A; Department of Biology, Jacksonville State University, Jacksonville, AL, United States.
  • Guerrero Pacheco S; Department of Biology, Jacksonville State University, Jacksonville, AL, United States.
  • Kondo T; National Cancer Center, Tokyo, Japan.
  • Su L; Department of Biology, Jacksonville State University, Jacksonville, AL, United States.
Front Cell Dev Biol ; 12: 1422452, 2024.
Article en En | MEDLINE | ID: mdl-39045458
ABSTRACT
The SS18-SSX fusion protein is an oncogenic driver in synovial sarcoma. At the molecular level, SS18-SSX functions as both an activator and a repressor to coordinate transcription of different genes responsible for tumorigenesis. Here, we identify the proto-oncogene FYN as a new SS18-SSX target gene and examine its relation to synovial sarcoma therapy. FYN is a tyrosine kinase that promotes cancer growth, metastasis and therapeutic resistance, but SS18-SSX appears to negatively regulate FYN expression in synovial sarcoma cells. Using both genetic and histone deacetylase inhibitor (HDACi)-based pharmacologic approaches, we show that suppression of SS18-SSX leads to FYN reactivation. In support of this notion, we find that blockade of FYN activity synergistically enhances HDACi action to reduce synovial sarcoma cell proliferation and migration. Our results support a role for FYN in attenuation of anti-cancer activity upon inhibition of SS18-SSX function and demonstrate the feasibility of targeting FYN to improve the effectiveness of HDACi treatment against synovial sarcoma.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Dev Biol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Dev Biol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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