In the course of this thesis, different therapeutic options were tested for their efficacy against glioblastoma in combination with a YB-1 dependent adenoviral construct, namely XVir-N-31. It was found that a combination of an CDK4/6 inhibitor (LEE011) and bromodomain inhibitor (JQ1), led to a highly significant increase in all viral parameters, like viral replication, potency and infectious particle formation. Both drugs can cross the blood-brain barrier and are already effective in doses that can be reached in the brain. This represents a new translation therapeutic approach.
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In the course of this thesis, different therapeutic options were tested for their efficacy against glioblastoma in combination with a YB-1 dependent adenoviral construct, namely XVir-N-31. It was found that a combination of an CDK4/6 inhibitor (LEE011) and bromodomain inhibitor (JQ1), led to a highly significant increase in all viral parameters, like viral replication, potency and infectious particle formation. Both drugs can cross the blood-brain barrier and are already effective in doses that...
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