Beta4 integrin promotes osteosarcoma metastasis and interacts with ezrin.

Abstract

The development of pulmonary metastasis is the major cause of death in osteosarcoma, and its molecular basis is poorly understood. In this study, we show that beta4 integrin is highly expressed in human osteosarcoma cell lines and tumor samples. Furthermore, highly metastatic MNNG-HOS cells have increased levels of beta4 integrin. Suppression of beta4 integrin expression by shRNA and disruption of beta4 integrin function by transfection of dominant-negative beta4 integrin was sufficient to revert this highly metastatic phenotype in the MNNG-HOS model without significantly affecting primary tumor growth. These findings suggest a role for beta4 integrin expression in the metastatic phenotype in human osteosarcoma cells. In addition, we identified a previously uncharacterized interaction between beta4 integrin and ezrin, a membrane-cytoskeletal linker protein that is implicated in the metastatic behavior of osteosarcoma. The beta4 integrin-ezrin interaction appears to be critical for maintenance of beta4 integrin expression. These data begin to integrate ezrin and beta4 integrin expression into a model of action for the mechanism of osteosarcoma metastases.

• Authors: X Wan, S Y Kim, L M Guenther, A Mendoza, J Briggs, C Yeung, D Currier, H Zhang, C Mackall, W-J Li, R S Tuan, A T Deyrup, C Khanna, L Helman
• Journal: Oncogene (Oncogene) Vol. 28 Issue 38 Pg. 3401-11 (Sep 24 2009) ISSN: 1476-5594 [Electronic] England
• PMID: 19597468 (Publication Type: Journal Article, Research Support, N.I.H., Intramural)

Chemical References

• Cytoskeletal Proteins
• Integrin beta4
• ezrin

Topics

• Bone Neoplasms (pathology)
• Cell Line, Tumor
• Cytoskeletal Proteins (physiology)
• Humans
• Integrin beta4 (analysis, physiology)
• Osteosarcoma (secondary)