The University of Minnesota Foundation recently highlighted the impact of Rein in Sarcoma Foundation and Zach Sobiech Fund in funding University researchers to identify potential proteins to target osteosarcoma treatments.
Article writer Nicole Endres writes “For Masonic Cancer Center scientists Branden Moriarity and David Largaespada, it’s about the Wyckoffs, the Sobiechs, and thousands of other families who are all too familiar with osteosarcoma and its devastating effects.”
These families fuel the researchers’ passion to cure this often deadly form of bone cancer. And they recently got a little closer to that goal.
New models developed at the Masonic Cancer Center, University of Minnesota with support from Rein in Sarcoma, reveal the genes and pathways that, when altered, can cause osteosarcoma. The information could be used to better target treatments for the often-deadly type of cancer. The new research was published May 11, 2015 in Nature Genetics.
“Human osteosarcoma tumors are so genetically disordered it is nearly impossible to utilize usual methods to identify the genes associated with them,” said first author Branden Moriarity, Ph.D., researcher in the Masonic Cancer Center and the University of Minnesota Medical School’s Department of Pediatrics. “This model offers the first opportunity to understand and research the genetics and drivers of osteosarcoma.” In March 2015, RIS again awarded new osteosarcoma research funding to Dr. Moriarity.
Moriarity partnered with researchers in the lab of David Largaespada, Ph.D., also with the Masonic Cancer Center and UMN Medical School’s Department of Pediatrics. The researchers utilized the “Sleeping Beauty” method to develop the cancer model, a technique developed by the Largaespada lab in 2005 and now used widely around the world.
The comprehensive genomic analysis uncovered several osteosarcoma genes which make proteins that could be targets for therapies in the future, such as SEMA4D and SEMA6D. SEMA4D and SEMA6D were found to be expressed at high levels in over half of all human osteosarcomas. Slowing or inhibiting the expression of SEMA4D could help stop the growth of osteosarcoma.
“SEMA4D seems to cause many human osteosarcomas to grow out of control,” said Largaespada. “We think, in the future, osteosarcomas could be targeted using monoclonal antibodies versus SEMA4D.” Targeted antibodies for SEMA4D are in clinical trials for other solid tumors. The discovery of its relationship to osteosarcoma could pave the way for future trials in patients with osteosarcoma.
This work was supported by funding from the National Cancer Institute, the American Cancer Society, the Rein in Sarcoma Foundation, and the Zach Sobiech Osteosarcoma Fund of the Children’s Cancer Research Fund. Largaespada is an American Cancer Society Research Professor. Moriarity is the recipient of the American Association for Cancer Research-Aflac, Inc. Career Development Award for Pediatric Cancer.
As he fought osteosarcoma, Zach Sobiech, collaborated often with Rein in Sarcoma. Part of his legacy was his donation of the guitar version of his very popular “Clouds” as the soundtrack of our video “From Never Heard of it, to We Caught it Early.”