Abstract |
We analyzed the expression of proteases and the clinicopathologic significance in non-skull base chordoma (NSBC). By using immunohistochemical techniques, we studied the expression of matrix metalloproteinase (MMP)-1, MMP-2, MMP-9, cathepsin B (CatB), and urokinase plasminogen activator (uPA) in 29 NSBCs and compared these data with clinicopathologic parameters and the expression of cell differentiation markers. Expression of MMP-1 (P = .092), MMP-2 (P = .041), and CatB (P = .058) was associated with nuclear pleomorphism, a previously described adverse prognostic indicator. Expression of cytokeratin 8 correlated with that of MMP-1 (P = .005), MMP-2 (P = .002), and uPA (P = .032). Patients with higher MMP-2 expression had a poorer prognosis than those with lower MMP-2 expression (P = .013). We believe that NSBCs with nuclear pleomorphism or stronger epithelial character have a higher invasive ability than those without. In addition, high MMP-2 expression was an indicator of an unfavorable clinical outcome in NSBC.
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Authors | Takahiko Naka, Carsten Boltze, Doerthe Kuester, Torss-Oliver Schulz, Amir Samii, Christian Herold, Helmut Ostertag, Albert Roessner |
Journal | American journal of clinical pathology
(Am J Clin Pathol)
Vol. 122
Issue 6
Pg. 926-30
(Dec 2004)
ISSN: 0002-9173 [Print] England |
PMID | 15539385
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Keratins
- Urokinase-Type Plasminogen Activator
- Cathepsin B
- Matrix Metalloproteinases
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Bone Neoplasms
(enzymology, mortality, pathology)
- Cathepsin B
(biosynthesis)
- Chordoma
(enzymology, mortality, pathology)
- Humans
- Immunohistochemistry
- Keratins
(metabolism)
- Matrix Metalloproteinases
(biosynthesis)
- Middle Aged
- Prognosis
- Survival Analysis
- Urokinase-Type Plasminogen Activator
(biosynthesis)
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