Stromal Expression of MMP-13 Is Required for Melanoma Invasion and Metastasis

Tumor invasion and metastasis of malignant melanoma have been shown to require proteolytic degradation of the extracellular environment achieved primarily by enzymes of the matrix metalloproteinases (MMP) family. We have earlier shown that increased enzyme activity is localized at the border of tumo...

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Veröffentlicht in:Journal of investigative dermatology 2009-11, Vol.129 (11), p.2686-2693
Hauptverfasser: Zigrino, Paola, Kuhn, Isolde, Bäuerle, Tobias, Zamek, Jan, Fox, Jay W., Neumann, Susanne, Licht, Alexander, Schorpp-Kistner, Marina, Angel, Peter, Mauch, Cornelia
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container_issue 11
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container_title Journal of investigative dermatology
container_volume 129
creator Zigrino, Paola
Kuhn, Isolde
Bäuerle, Tobias
Zamek, Jan
Fox, Jay W.
Neumann, Susanne
Licht, Alexander
Schorpp-Kistner, Marina
Angel, Peter
Mauch, Cornelia
description Tumor invasion and metastasis of malignant melanoma have been shown to require proteolytic degradation of the extracellular environment achieved primarily by enzymes of the matrix metalloproteinases (MMP) family. We have earlier shown that increased enzyme activity is localized at the border of tumor cells and the adjacent peritumoral connective tissue, emphasizing the importance of tumor-stroma interactions in the regulation of MMP activity. To confirm the role of stroma-derived MMP-13 in the invasion process, we investigated the invasiveness of melanoma cells upon intradermal injection in mice with complete inactivation of MMP-13. Tumor growth was significantly impaired in mmp-13−/- mice and most significant at early time points as compared with wild-type littermates. Moreover, metastasis to various organs was reduced to 17.6 vs 30% in lungs, 2.9 vs 30% in the liver. Strikingly, ablation of MMP-13 completely abrogated formation of metastasis in the heart (0 vs 40%). Notably, decreased tumor growth in mmp-13−/- mice was associated with reduced blood vessel density. In addition, decreased blood vessel permeability in the tumors was measured by magnetic resonance imaging of tumor-bearing animals. These data suggest an important role of MMP-13 in tumor growth and an unexpected role in organ-specific metastasis of melanoma cells.
doi_str_mv 10.1038/jid.2009.130
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subjects Animals
Biological and medical sciences
Dermatology
Endothelial Cells - enzymology
Endothelial Cells - pathology
Gene Expression Regulation, Enzymologic - physiology
Macrophages - pathology
Matrix Metalloproteinase 13 - genetics
Matrix Metalloproteinase 13 - metabolism
Medical sciences
Melanoma - immunology
Melanoma - physiopathology
Melanoma - secondary
Mice
Mice, Inbred C57BL
Mice, Mutant Strains
Neoplasm Transplantation
Neovascularization, Pathologic - immunology
Neovascularization, Pathologic - pathology
Neovascularization, Pathologic - physiopathology
Neutrophils - pathology
Skin Neoplasms - immunology
Skin Neoplasms - pathology
Skin Neoplasms - physiopathology
Stromal Cells - enzymology
Stromal Cells - pathology
Tumors of the skin and soft tissue. Premalignant lesions
title Stromal Expression of MMP-13 Is Required for Melanoma Invasion and Metastasis
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