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Cell surface glycosaminoglycans of a tumor cell line and its DNA transfected variant differing in their lung colonizing potential

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Abstract

A highly lung-colonizing cell line RMS/82 was obtained by DNA transfection from a low lung-colonizing line RMS/8, a clone of a rat rhabdomyosarcoma cell line. The cells were metabolically labeled with3H-glucosamine and35S-sulfate. The newly synthesized pericellular glycosaminoglycans and the ability of the cells from the two lines to degrade extracellular matrix components were studied comparatively. The following conclusions were obtained: 1) Thein vitro proliferation rate is not a determinant in the modulation of the colonizing potential of these cells; 2) The strongly colonizing RMS/82 cells release more radioactivity from the radiolabeled extracellular matrix than their weakly colonizing counterparts; 3) The cells with a high colonizing potential incorporated less radioactivity into the cell surface glycosaminoglycans, and exhibited a lower heparan sulfate to chondroitin sulfate ratio than the weakly colonizing RMS/8 line.

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Abbreviations

RMS:

rhabdomyosarcoma

ECM:

extracellular matrix

GAGs:

glycosaminoglycans

DMEM:

Dulbecco's modified essential medium

FCS:

fetal calf serum

PBS:

phosphate buffered saline

CPC:

cetylpyridinium chloride

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Redini, F., Verrelle, P., Hillova, J. et al. Cell surface glycosaminoglycans of a tumor cell line and its DNA transfected variant differing in their lung colonizing potential. Glycoconjugate J 4, 191–201 (1987). https://doi.org/10.1007/BF01049456

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  • DOI: https://doi.org/10.1007/BF01049456

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