Active detachment involves inhibition of cell-matrix contacts of malignant melanoma cells by secretion of melanoma inhibitory activity

Bosserhoff, Anja-Katrin and Stoll, Raphael and Sleeman, Jonathan P. and Bataille, Frauke and Buettner, Reinhard and Holak, Tad A. (2003) Active detachment involves inhibition of cell-matrix contacts of malignant melanoma cells by secretion of melanoma inhibitory activity. LABORATORY INVESTIGATION, 83 (11). pp. 1583-1594. ISSN 0023-6837

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Abstract

Melanoma inhibitory activity (MIA) has been identified as a small protein secreted from malignant melanoma cells. Recent results revealed a direct interaction of MIA and epitopes within extracellular matrix proteins including fibronectin. The aim of this study was to analyze functional consequences mediated by this interaction. Here we show that MIA interferes specifically with attachment of melanoma cells to fibronectin, a phenomenon we refer to as active detachment. Antibodies inhibiting binding of alpha4beta1 and alpha5beta1 integrins to fibronectin cross-react specifically with MIA, suggesting that MIA shares significant structural homology with the binding pockets of these integrins and thereby masks the respective epitopes on extracellular matrix molecules. Several peptides derived from fibronectin and from a phage display screening were tested with respect to a potential MIA-inhibitory effect. In vitro tests identified two peptides affecting MIA function; both inhibited growth of melanoma metastases in vivo. In summary, we conclude that MIA may play a role in tumor progression and spread of malignant melanomas via mediating active detachment of cells from extracellular matrix molecules within their local milieu. Further, our results suggest that inhibiting MIA functions in vivo may provide a novel therapeutic strategy for metastatic melanoma disease.

Item Type: Article
Uncontrolled Keywords: HEPARIN-BINDING DOMAIN; INTEGRIN ALPHA-4-BETA-1; ACTIVITY MIA; ACTIVITY PROTEIN; TUMOR-CELLS; EXPRESSION; FIBRONECTIN; GROWTH; ADHESION; IDENTIFICATION;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Pathologie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 30 Aug 2021 08:00
Last Modified: 30 Aug 2021 08:00
URI: https://pred.uni-regensburg.de/id/eprint/38478

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