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[Cancer Research 46, 3624-3629, July 1, 1986]
© 1986 American Association for Cancer Research

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Differential Adhesiveness of Rhabdomyosarcoma-derived Cloned Metastatic Cell Lines to Vascular Endothelial Monolayers

Stéphane Korach1, Marie-France Poupon, Jean-Antoine Du Villard and Margaret Becker

UA 1158, C. N. R. S. [S. K., J. A. V.], and Institut de Recherches Scientifiques sur le Cancer [M. F. P., M. B.], 94 802 Villejuif, France

A series of 11 cloned cell lines derived from a primary, nickel-induced rat rhabdomyosarcoma was evaluated for their metastatic capacity (number of lung colonies following i.v. injection) and attachment kinetics to confluent pig endothelial cell monolayers grown in vitro. The morphology of the adhering cells was also studied by optical and scanning electron microscopy.

Cells from all lines tested began to attach to the endothelial monolayers within 15 min of incubation at 37°C, with 64% to 93% of the cells adhering after 2 h. Attachment rates at 30 min ranged from 29 to 48% for four lines classed as "weakly adhesive" (attachment, <50%) and from 53 to 78% for seven lines classed as "highly adhesive" (attachment, >50%).

Four clones of five displaying low lung-colonizing capacities also showed low attachment rates to endothelial monolayers in vitro. All of six highly colonizing lines studied had high attachment rates.

A degree of positive correlation was observed between the amount of cell surface fibronectin as evaluated by immunofluorescence and the early phase attachment rates (and lung-colonizing capabilities) of the different cloned cell lines.

Early (15 min) attachment of tumor cells to isolated extracellular matrix preparations proceeded at higher rates than to endothelial monolayers, and previously detected differences between high- and low-colonizing clones were less evident with these matrix substrates.

Our results suggest possible interrelationships between specific cell adhesion properties and the metastatic potential of blood-borne tumor cells.

1 To whom requests for reprints should be addressed, at UA 1158, C. N. R. S., B. P. No. 8, 94802 Villejuif, France.

Received 8/ 6/85. Revised 2/13/86. Accepted 3/20/86.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1986 by the American Association for Cancer Research.