Pediatric rhabdomyosarcoma is a type of cancerous tumor that arises in the soft tissue, such as muscles, though the origin of one of the most aggressive subtypes is unclear. Scientists at St. Jude Children’s Research Hospital showed in proof-of-concept models that expressing one mutated hybrid “fusion” oncoprotein in either muscle or blood vessel (endothelial) cells produced these aggressive tumors, which were molecularly identical. The findings, which have implications for treating aggressive rhabdomyosarcoma, were published today in Nature Communications.
Rhabdomyosarcoma expressing a hybrid protein from the fusion of two genes, PAX3 and FOXO1, is referred to as fusion-positive. Pediatric fusion-positive rhabdomyosarcoma has a dismal prognosis. Rhabdomyosarcoma cells appear muscle-like; however, fusion-positive tumors can form in areas without skeletal muscle. Not knowing where the cancerous fusion-positive cells come from can limit research and treatment options. This St. Jude study generated models to find where and how these fusion-positive tumors arise, ultimately providing clues for ways to stop this cancer.
“There’s a subset of these patients with rhabdomyosarcoma that we don’t know where the tumors come from,” said corresponding author Mark Hatley, M.D., Ph.D., St. Jude Department of Oncology. “Our new models will allow us to shed light on their origin so that we can better treat them.”
Fusion overrides fate to cause rhabdomyosarcoma
Fusion-positive rhabdomyosarcoma appears diffuse within the body, looking similar to metastatic disease. Historically, researchers attempted to find a primary muscle tumor to find a more effective way to counter this subtype by identifying its cell of origin. All such efforts to date have been unsuccessful.
Hatley’s lab took a different approach. Previously, they showed fusion-negative rhabdomyosarcoma could come from non-muscle cells. The researchers wondered if that was also possible for the more aggressive subtype. Therefore, they created a mouse model expressing the PAX3-FOXO1 fusion oncoprotein in blood vessel cells. They compared this to a previously established mouse model of fusion-positive rhabdomyosarcoma that arises from muscle cells. These mouse models enabled the researchers to see if they could find traces of the original cell type when presented with fusion-positive tumors from each model, thus distinguishing their origins and identifying potential vulnerabilities.
“We showed this fusion oncoprotein is such a potent rhabdomyosarcoma driver, it can overwrite a cell’s identity,” said co-author Brian Abraham, Ph.D., St. Jude Department of Computational Biology, whose lab performed much of the bioinformatics analysis in collaboration with the St. Jude Center for Applied Bioinformatics. “It overrode any sort of normal differentiation processes, in either muscle or endothelial cells, and forced those cells to become tumor-like.”
Finding faults in fusion-positive rhabdomyosarcoma
The study indicates that it may not be possible to find the cellular origin of these cancerous cells and identify potential drug targets using those methods. Instead, focusing on the fusion oncoprotein’s effects may be a better way to identify potential therapeutic interventions.
The Hatley lab, therefore, created a model to look at the genetic and epigenetic effects of the fusion oncoprotein more closely. They exploited the oncoprotein’s strength as a cancer driver in induced pluripotent stem cells. These cells have the capability of differentiating into any cell type. The scientists first differentiated the cells into endothelial cells and then added the fusion oncoprotein. This in vitro system allows them to look even closer at what happens when these cells become tumor-like.
Abraham’s lab found that the fusion oncoprotein was still acting as a powerful activator of muscle cell fate in the system. The aberrant protein bound to DNA regions that enhanced expression of genes well-known to be major regulators of muscle cell development, such as MYOD1. These findings serve as a proof-of-concept that the system can find downstream targets of the oncoprotein and increase confidence in any future novel targets found by the method.
Authors and funding
The study’s co-first authors are Madeline Searcy*, formerly of St. Jude, and Randolph Larsen IV*, of St. Jude. The study’s other authors are Bradley Stevens*, Yang Zhang, Hongjian Jin, Catherine Drummond, Casey Langdon, Katherine Gadek, Kyna Vuong, Kristin Reed, Matthew Garcia, Beisi Xu, Darden Kimbrough, Grace Adkins*, Nadhir Djekidel, Shaina Porter, Patrick Schreiner, Shondra Pruett-Miller and Jerold E. Rehg, all of St. Jude.
*Student in the St. Jude Children’s Research Hospital Graduate School of Biomedical Sciences during the research.
The study was supported by grants from the Damon Runyon-Sohn Pediatric Cancer Fellowship (DRSG-30-19), the National Cancer Institute (R01CA216344, R01CA251436 and F31CA250398), V Foundation for Cancer Research, the Rally Foundation for Childhood Cancer Research and Open Hands Overflowing Hearts (20IC23), St. Jude Cancer Center Support Grant (P30 CA21765) and ALSAC, the fundraising and awareness organization of St. Jude.
St. Jude Children’s Research Hospital
St. Jude Children’s Research Hospital is leading the way the world understands, treats and cures childhood cancer, sickle cell disease and other life-threatening disorders. It is the only National Cancer Institute-designated Comprehensive Cancer Center devoted solely to children. Treatments developed at St. Jude have helped push the overall childhood cancer survival rate from 20% to 80% since the hospital opened more than 60 years ago. St. Jude shares the breakthroughs it makes to help doctors and researchers at local hospitals and cancer centers around the world improve the quality of treatment and care for even more children. To learn more, visit stjude.org, read St. Jude Progress blog, and follow St. Jude on social media at @stjuderesearch. (VP/Newswise)
