| Autor: |
Di Virgilio S; Department of General Chemistry I, Université Libre de Bruxelles, Brussels, Belgium., Hellmann KP, Robberecht P, Bruyneel EA, Van Dessel G, Rampelberg M, Mareel MM, Hooghe R, Gabius HJ |
| Jazyk: |
angličtina |
| Zdroj: |
Anticancer research [Anticancer Res] 1991 Sep-Oct; Vol. 11 (5), pp. 1815-21. |
| Abstrakt: |
A low-metastatic, glycosylation-defective variant of the B16 murine melanoma was obtained by Tao and Burger (1977) through selection with wheat germ agglutinin. We found that variant and parental (wild-type) cell lines were equally invasive when confronted with precultured embryonic chick heart fragments in vitro. Also, a short-term in vivo arrest assay showed no significant differences. After intravenous injection, wild-type cells killed the recipient mice faster than did the variant cells. We were able to confirm the changes in glycosylation at the enzyme level. In addition, we showed that the pattern of endogenous lectins was strikingly different, at least at the quantitative level. We also looked at another set of receptor proteins, namely receptors for neurotransmitters coupled to adenylate cyclase. The response to the vasoactive intestinal peptide and prostaglandins was lower in the variant cells, which also had a delayed response to cholera toxin. Although most of the data can be explained by altered glycosylation in the variant cells, the large number of differences between variant and parent cells makes it difficult to identify the biochemical basis of altered metastatic behaviour. This might also be the case with other pairs of cells differing in metastatic activity. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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