Osteosarcoma (OS) is an aggressive primary bone malignancy with peak incidence in children and adolescents.Despite current multimodal treatments, there has been little change in overall survival outcomes in the last two decades.The canonical Wnt/β-catenin pathway is known to be a critical pathway in OS progression.To better understand the molecular basis of OS and potentially provide target/s for new therapies or diagnostics, we investigated the relationship between β-catenin, more specifically, the transcriptionally active form of β-catenin, Activated β-Catenin (ABC), and OS progression.We previously reported an association between ABC and aggressive OS whereby, cellular/nuclear ABC levels, but not cellular/nuclear β-catenin levels, increase with the degree of aggressiveness.However, a direct role for ABC in promoting OS progression has never been shown.In order to directly determine the role/impact of ABC in OS progression, we generated a pEGFP-ABC fusion construct which simulates ABC's phosphorylation pattern.Transfection of pEGFP-ABC, pEGFP-β-catenin, or an empty vector (pEGFP-C2) into OS cell lines showed that wnt pathway transcriptional activity in GFP-ABCexpressing cells was significantly higher than that in both GFP-β-catenin and emptyvector-transfected cells.We also show that the in vitro invasive potential of the pEGFP-ABC-transfected cells was significantly higher compared to both pEGFP-βcatenin and pEGFP-transfected cells.To the best of our knowledge, this is the first report that shows that ABC, and not β-catenin, directly drives transcriptional activity of the Wnt/β-catenin pathway to enhance OS aggressiveness and promote an invasive phenotype.
Hinton et al. (Mon,) studied this question.