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Published on: August 10, 2017
Combination of HDAC and FYN inhibitors in synovial sarcoma treatment
Kyra Parker1, Yanfeng Zhang2, Gavin Anchondo1
1Department of Biology, Jacksonville State University, Jacksonville, AL, United States.
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.
Insights
Researchers found that inhibiting the SS18-SSX fusion protein reactivates FYN, a gene promoting cancer. Targeting FYN enhances cancer therapy effectiveness in synovial sarcoma.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genetics
Background:
- Synovial sarcoma is driven by the SS18-SSX fusion protein, which regulates gene transcription.
- SS18-SSX acts as both a transcriptional activator and repressor in tumorigenesis.
Purpose of the Study:
- To identify new SS18-SSX target genes.
- To investigate the role of the proto-oncogene FYN in synovial sarcoma and its therapeutic implications.
Main Methods:
- Identification of FYN as a novel SS18-SSX target gene.
- Genetic and pharmacologic approaches using histone deacetylase inhibitors (HDACi).
- Assessment of FYN activity blockade in combination with HDACi.
Main Results:
- SS18-SSX negatively regulates FYN expression in synovial sarcoma cells.
- Suppression of SS18-SSX leads to FYN reactivation.
- Blocking FYN activity synergistically enhances HDACi efficacy in reducing synovial sarcoma cell proliferation and migration.
Conclusions:
- FYN plays a role in attenuating anti-cancer activity when SS18-SSX function is inhibited.
- Targeting FYN is a feasible strategy to improve HDACi treatment effectiveness for synovial sarcoma.
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