## Abstract Matrix metalloproteinaseβ9 (MMPβ9) is a wellβknown regulator and effecter of many cellular processes including wound healing. In the cornea, either too much or too little MMPβ9 can be detrimental to overall wound repair. We investigated the secreted factors as well as the intracellular
Matrix metalloproteinase-9 (MMP-9) expression in childhood osseous osteosarcoma
β Scribed by Himelstein, Bruce P.; Asada, Naohiro; Carlton, Martha R.; Collins, Margaret H.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 520 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0098-1532
No coin nor oath required. For personal study only.
β¦ Synopsis
Background. Over 80% of patients with osteosarcoma treated with excision alone develop pulmonary metastases, suggesting that the majority of patients with this disease harbor ''micrometastases'' at diagnosis. There are no histologic or molecular variables which can predict the presence or absence of micrometastasis. Matrix metalloproteinases (MMPs) are a class of matrix-and basement membranedegrading enzymes whose expression is associated with tumor cell invasive and metastatic behavior. One of these enzymes, MMP-9 or gelatinase B, is expressed in developing and remodeling bone and in osteosarcoma cell lines. We speculated that MMP-9 expression might be associated with the micrometastatic behavior of osteosarcoma. Procedure. We ex-amined a series of pediatric primary osseous osteosarcomas and metastases for the expression of MMP-9, using a monoclonal antibody. Results. We found intense MMP-9 immunostaining in most tumor cells in all samples of pretreatment osteosarcomas. In all postchemotherapy resection samples, tumor cells stained similarly, but there were fewer positively staining cells overall. In 4 of 5 metastastic lesions examined, intense immunostaining for MMP-9 was detected. Conclusions. These results suggest that MMP-9 expression is common in osteosarcoma, and that further study of the role of MMP-9 in pediatric osteosarcoma behavior is warranted. Med.
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