Childhood Cancer

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Development and Characterization of Novel Models of Human Osteosarcoma Development and Metastasis

Institution: 
University of Minnesota
Researcher(s): 
Beau Webber, PhD
Grant Type: 
Young Investigator Grants
Year Awarded: 
2017
Type of Childhood Cancer: 
Osteosarcoma
Project Description: 

Background

Osteosarcoma is the most common cancer of the bone in children and adolescents, with approximately 900 new cases annually in the United States. It occurs largely in growing adolescents and young adults, with the highest incidence at the age of 15-19-years-old. Surgery, chemotherapy, and radiation remain the most common therapeutic interventions but are associated with significant side effects that negatively impact patient quality of life. A better understanding of the genetic mechanisms and underlying biological events involved in the initiation and development of osteosarcoma would pave the way for the development of new therapies. However, effective models of human osteosarcoma initiation and development are not available and thus these fundamental questions go unanswered. 

Project Goal:

The current proposal will implement cutting edge technologies in the area of pluripotent stem cell-based tissue engineering to replicate bone formation in a dish, and couple this strategy with advanced methods for genome engineering to model mutations that are suspected to promote the formation of osteosarcoma. This system will represent a novel and highly impactful platform for functional studies elucidating the mechanisms underlying human osteosarcoma initiation, development, and metastasis. Additionally, while the current proposal focuses on osteosarcoma, in theory, our pluripotent stem cell-based platform can be used to model cancers derived from nearly any tissue type.  Consequently, the proposed research has far-reaching implications for the way all human cancers are studied and will undoubtedly foster the development of clinically relevant therapeutic interventions.

Project Update 2018

Over the first year of ALSF support, we have made substantial progress in our efforts to model osteosarcoma (OS) development with human induced pluripotent stem cells (iPSC). We have successfully implemented cutting edge genetic engineering technologies such as CRISPR/Cas9 in order to “install” mutations that are implicated in OS, and are now using tissue engineering technologies to convert our iPSC into the cells that make bone (osteoblasts). Our ultimate goal is to create a “bottom-up” model of OS development that we can observe and manipulate in the laboratory. This will allow us to gain a greater understanding of what causes OS to form, and why OS is more difficult to treat in some patients than others. Most importantly, this model and the knowledge gained from it will ultimately allow more rapid testing of new therapeutic interventions.

Project Update 2019

Through two years of ALSF support, we have made substantial progress in our efforts to model osteosarcoma (OS) development with human induced pluripotent stem cells (iPSC). We have further characterized the cell types present in the iPSC-MSC cultures, allowing us to focus on specific bone stem cells that are implicated as a precursor of OS. With optimized gene engineering methods, we installed mutations implicated in OS and are evaluating the impact of these mutations using in vitro, and very soon, in vivo functional assays. Our ultimate goal is to create a “bottom-up” model of OS development that we can observe and manipulate in the laboratory. This will allow us to gain a greater understanding of what causes OS to form, and why some patient’s OS is more difficult to treat than others. Most importantly, this model and the knowledge gained from it will ultimately allow more rapid testing of new therapeutic interventions.

 
Co-funded by: 
Northwestern Mutual Foundation