期刊
PHARMACOLOGICAL REPORTS
卷 62, 期 2, 页码 414-423出版社
POLISH ACAD SCIENCES INST PHARMACOLOGY
DOI: 10.1016/S1734-1140(10)70283-8
关键词
PAMAM dendrimer; digoxin; proscillaridin A; breast cancer; anticancer drugs
The objective of this study was to determine the cytotoxicity, antiproliferative activity, and apoptosis induction activity of two modified glycosides - digoxin and proscillaridin A - conjugated to a generation 3 polyamidoamine dendrimer (G3 PAMAM-NH2) in human breast cancer cells. The results suggest that conjugation with the G3 PAMAM-NH2, dendrimer enhances the cytotoxicity of modified digoxin and proscillaridin A both in MCF-7 and in MDA-MB-231 breast cancer cells. Additionally, the conjugate-induced apoptosis was significantly greater than apoptosis evoked by free modified digoxin and proscillaridin A.
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