Inhibition of Melanoma Cell Binding to Type IV Collagen by Analogs of Cell Adhesion Regulator

Integrin-mediated tumor cell adhesion to type IV collagen is believed to play a role in the invasion of basement membrane proteins and the subsequent metastatic process. The cellular protein CAR (cell adhesion regulator) has been proposed to influence integrin-mediated binding to extracellular matri...

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Veröffentlicht in:Journal of medicinal chemistry 1997-09, Vol.40 (19), p.3077-3084
Hauptverfasser: Lauer, Janelle L, Furcht, Leo T, Fields, Gregg B
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Sprache:eng
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Zusammenfassung:Integrin-mediated tumor cell adhesion to type IV collagen is believed to play a role in the invasion of basement membrane proteins and the subsequent metastatic process. The cellular protein CAR (cell adhesion regulator) has been proposed to influence integrin-mediated binding to extracellular matrix proteins, including basement membrane (type IV) collagen. Three analogs of the CAR138 - 142 have been tested for activity. The first contains the 138−142 sequence (CAR138 - 142, Val-Glu-Ile-Leu-Tyr-NH2), the second contains the 138−142 sequence with a phosphorylated Tyr [pCAR138 - 142, Val-Glu-Ile-Leu-Tyr(PO3H2)-NH2], and the third contains the reversed 138−142 sequence (rCAR138 - 142, Tyr-Leu-Ile-Glu-Val-NH2). When added extracellularly, none of the analogs had a significant affect on cell adhesion to type IV collagen. Using a novel reversible cell permeabilization method, we found that intracellular incorporation of both CAR138 - 142 and pCAR138 - 142 resulted in inhibition of cell adhesion in a dose-dependent fashion. The IC50 values were ∼90 and ∼10 μM for CAR138 - 142 and pCAR138 - 142, respectively. Intracellular incorporation of the rCAR138 - 142 peptide had no affect on cell adhesion. Fluorescence microscopy of a fluorescein-labeled CAR138 - 142 peptide revealed that the reversible permeabilization procedure resulted in the peptides crossing the cell membrane. Affinity chromatography of melanoma cell lysates with pCAR138 - 142 or rCAR138 - 142 attached to a solid support of magnetic beads suggested that one protein was bound uniquely by pCAR138 - 142. Immunoprecipitation analysis identified vinculin, a protein associated with the actin cytoskeleton, as the protein specifically bound by pCAR138 - 142. Immunoprecipitation with pp125 FAK - or β1-integrin-derived mAbs gave negative results. Our study suggests that a possible therapeutic approach for inhibition of melanoma cell adhesion adhesion to extracellular matrix proteins is the use of CAR peptide analogs intracellularly.
ISSN:0022-2623
1520-4804
DOI:10.1021/jm970206j