Author/Authors :
A Cipollone، نويسنده , , Marco Berettoni، نويسنده , , T. Bigioni، نويسنده , , L. Binaschi، نويسنده , , C Cermele، نويسنده , , E Monteagudo، نويسنده , , L Olivieri، نويسنده , , D Palomba، نويسنده , , Fabio Animati، نويسنده , , C Goso، نويسنده , , C.A Maggi، نويسنده ,
Abstract :
Several observations highlight the importance of the carbohydrate moiety for the biological activity of antitumoural anthracyclines. Here is reported the synthesis, cytotoxicity and topoisomerase II-mediated DNA cleavage intensity of the new oligosaccharide anthracyclines 1–4 modified in the sugar residue. Evaluation of cytotoxic potency on different cell lines, resulted in quite similar values among the different analogues. On the other hand, topoisomerase II-mediated DNA breaks level was different for the various compounds, and was not related to cytotoxicity, thus supporting previous observations reported for some monosaccharide anthracyclines modified in the carbohydrate portion.