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pubmed-article:16015389pubmed:abstractTextMultiple myeloma (MM) is an incurable B-cell cancer characterised by the monoclonal proliferation of tumour cells in the bone marrow (BM). It has been described that matrix metalloproteinases (MMPs) and especially MMP-9 is secreted by MM cells. In this study, we investigated the possibility to exploit MMP-9 activity to activate prodrugs and to target MM cells as a new tumour-specific therapy. Cleavage of the prodrug EV1-FITC by MMP-9 resulted in release of fluorescence which can be used as a measure of prodrug activation. The 5T33MM mouse model was used in this proof-of-principle study. The prodrug was activated in a higher amount by addition to MMP-9-producing 5T33MMvv cells, homogenates from tumour-bearing organs (BM, spleen) and isolated 5T33MM-diseased BM and spleen cells compared to non-MMP-9-producing 5T33MMvt cells and homogenates/cells from non-tumour-bearing organs/mice, as measured by fluorescence release. This fluorescence release could be inhibited by the MMP-2/MMP-9-specific inhibitor, CTT. Activation of the prodrug in the 5T33MM spleen and BM homogenates was confirmed by chromatography. EV1-fluorescein isothiocyanate injection into 5T33MM-diseased animals resulted in a higher fluorescence release by the isolated BM and spleen cells compared to injection into healthy animals. In conclusion, MMP-9 activity can be used to activate prodrugs that target MM.lld:pubmed
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pubmed-article:16015389pubmed:pagination1628-33lld:pubmed
pubmed-article:16015389pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:16015389pubmed:year2005lld:pubmed
pubmed-article:16015389pubmed:articleTitleTargeting an MMP-9-activated prodrug to multiple myeloma-diseased bone marrow: a proof of principle in the 5T33MM mouse model.lld:pubmed
pubmed-article:16015389pubmed:affiliationDepartment of Haematology and Immunology, Vrije Universiteit Brussel (VUB), Brussels, Belgium.lld:pubmed
pubmed-article:16015389pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16015389pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:16015389pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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