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Growth-factor-dependent migration of human lung-cancer cells

✍ Scribed by Cecilia G. Bredin; Zhiwen Liu; Dan Hauzenberger; Julius Klominek


Publisher
John Wiley and Sons
Year
1999
Tongue
French
Weight
232 KB
Volume
82
Category
Article
ISSN
0020-7136

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✦ Synopsis


Human lung tumors express different types of growthfactor receptors and corresponding ligands that might modulate several biological functions such as proliferation, differentiation, adhesion, and chemotaxis. In the present study, we have investigated the expression of different growth-factor receptors and their ligands in 5 established human lungcancer cell lines. Using RT-PCR, we found that IGF-II/ mannose-6-phosphate (M6P), c-met, EGF and c-kit receptors are expressed in 5/5 human lung-cancer cell lines. In order to investigate the biological function of these receptors, we performed Boyden-chamber assays using various growth factors as chemo-attractants. Human non-small-cell-lungcancer cells (non-SCLC) migrated to recombinant human (rh)IGF I and IGF II at concentrations ranging from 1 to 1000 ng/ml, to HGF at 10 to 100 ng/ml, to EGF at 1 to 100 ng/ml and SCF at 1 to 50 ng/ml. In addition, we performed Boydenchamber assays using U-1810-, U-1752-and Wart-derived serum-free conditioned medium as chemo-attractants. Serum-free conditioned medium stimulated migration of producer cells in a dose-dependent manner. The autocrine motility stimulating effect of U-1810-derived serum-free conditioned medium could be inhibited by 50% in the presence of neutralizing ahIGF-II antibodies in the assay, suggesting a possible autocrine motility loop in vitro. Int.


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