Osteosarcoma models: from cell lines to zebrafish
- Authors
- Mohseny, A.B., Hogendoorn, P.C., and Cleton-Jansen, A.M.
- ID
- ZDB-PUB-120510-22
- Date
- 2012
- Source
- Sarcoma 2012: 417271 (Review)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 22566751 Full text @ Sarcoma
High-grade osteosarcoma is an aggressive tumor most commonly affecting adolescents. The early age of onset might suggest genetic predisposition; however, the vast majority of the tumors are sporadic. Early onset, most often lack of a predisposing condition or lesion, only infrequent (<2%) prevalence of inheritance, extensive genomic instability, and a wide histological heterogeneity are just few factors to mention that make osteosarcoma difficult to study. Therefore, it is sensible to design and use models representative of the human disease. Here we summarize multiple osteosarcoma models established in vitro and in vivo, comment on their utilities, and highlight newest achievements, such as the use of zebrafish embryos. We conclude that to gain a better understanding of osteosarcoma, simplification of this extremely complex tumor is needed. Therefore, we parse the osteosarcoma problem into parts and propose adequate models to study them each separately. A better understanding of osteosarcoma provides opportunities for discovering and assaying novel effective treatment strategies.