Scientists develop new treatment for soft-tissue childhood cancer

Scientists develop new treatment for soft-tissue childhood cancer Currently, long-term survival rates for synovial sarcoma are well below 50 per cent. 

Scientists in Ireland have developed a potential new therapeutic approach for synovial sarcoma, one of the most common soft-tissue cancers in teenagers and young adults.

At present the long-term survival rates for synovial sarcoma patients is well below 50 per cent; a fact that underlines just how important new discoveries are if we are to improve the outlook for patients and their families.
 
Using state-of-the-art CRISPR genome screening technology, the scientists first identified a protein (BRD9) as essential for the survival of synovial sarcoma tumours. They then set about designing new drugs to target this protein. Pre-clinical trials in mice showed that a newly developed drug blocks tumour progression. The next step will be to test the new drug in clinical trials with patients, which the scientists hope will take place in the near future.
 
Dr Gerard Brien, Research Fellow in Genetics at Trinity College Dublin and lead author of the research published in international journal eLIFE, set out to identify molecular vulnerabilities in synovial sarcoma tumours

Synovial sarcoma patients do not respond well to conventional treatment approaches, and therefore, like many other difficult-to-treat cancers, have low survival rates.


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At odds with the inability to cure synovial sarcoma is our knowledge of the genetic abnormality that causes the disease – for years scientists have known it is caused by a singular genetic mutation that occurs in 100 per cent of patients. This mutation creates a harmful protein (SS18-SSX) that is responsible for the cancer development. As a result, scientists reasoned that somehow impeding SS18-SSX would provide an ideal therapy. Until now, however, no such approaches had been developed.
 
In the current study, Dr Brien and colleagues used CRISPR-based genomic screening technologies to perform genetic screens to identify potential therapeutic vulnerabilities in synovial sarcoma tumours.
 
Significantly, they found a protein (BRD9) that is essential for the survival of synovial sarcoma cells. They confirmed through biochemical studies in synovial sarcoma cells that BRD9 partners with the disease-causing SS18-SSX protein, and thus supports it in driving cancer development. Next, using cutting-edge approaches to drug design, they created a new BRD9 degrader drug, and in pre-clinical trials in mice, they found that BRD9 degradation was successful in blocking the progression of synovial sarcoma tumours.

“As the term degrader suggests, the drug we created degrades the BRD9 protein, removing it from cancer cells,” Dr Gerard Brien said. “It essentially tricks the cells into eliminating this protein on which they rely, which in turn leads to their death.”

“Excitingly, our work demonstrates that degrading BRD9 impedes the SS18-SSX protein, which is the underlying cause of synovial sarcoma. We also found that our new drug primarily impacts cellular processes important in synovial sarcoma, but not normal cells.” 

“This is very important, because it should result in less unwanted side-effects in patients. We now hope these promising findings will lead to clinical trials of this new drug in patients in the near future,” he said.

Dr Gerard Brien is the 2018 Irish Cancer Society Biomedical Research Fellow, and recently returned to Trinity College Dublin to establish his own research laboratory. He trained at the Memorial Sloan Kettering Cancer Center (New York), Harvard Medical School and the Dana Farber Cancer Institute (Boston). His current research focuses on using CRISPR technologies and other molecular approaches to identify new therapeutic targets in pediatric cancers with a view to developing more effective and personalised cancer treatments.
Source: Trinity College Dublin. 

 
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