Childhood Cancer Research

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B-lapachone as a Novel Targeted Therapy for ATRTs and other Pediatric Cancers

Background


Atypical teratoid rhabdoid tumors (ATRTs) are highly lethal cancers that most commonly occur in the brain of young children. Despite maximally intense therapy, most patients with ATRTs die of their disease and the few children who survive are often significantly disabled due to the effects of radiation on their developing brains. Historically, using targeted therapies for ATRTs has been very difficult as the most common gene mutation in these cancers is not currently druggable.

Recently, our team has invented a series of novel targeted drugs (ß-lapachone and DNQ) that kill cancer cells after being activated by an enzyme (NQO1) that is present at very high levels in many adult cancers. These drugs have now entered clinical trials in adults with cancer.

Project Goals


Recently, we found that NQO1 is very highly expressed in ATRTs and not in the normal brain surrounding the tumor. Thus, this allows targeted therapy for ATRTs. Here we will complete the testing of these drugs for pediatric use. First, we will study a large panel of other pediatric cancers to determine the full extent of cancers that may be susceptible to these drugs. Next, we will confirm that these drugs are effective therapies in cell culture and mice with ATRTs. Finally, we will determine which of these drugs best penetrates into tumors in the brain to allow the selection of the best drug for pediatric patients. At the completion of this grant, we will open a clinical trial of one of these agents in children with ATRTs.

Project Team

University of Texas Southwestern Medical Center