In addition to membrane injury, an affinity for melanin might be involved in the high sensitivity of human melanoma cells to hederacolchiside A1

被引:15
作者
Debiton, E
Borel, M
Communal, Y
Mshvildadze, V
Barthomeuf, C
机构
[1] Univ Auvergne, Ctr Jean Perrin, INSERM, UMR 484, F-63005 Clermont Ferrand, France
[2] Fac Pharm Clermont Ferrand, Lab Pharmacognosy & Biotechnol, F-63001 Clermont Ferrand, France
[3] Ctr Jean Perrin, Lab Immunol & Cellular Therapy, Clermont Ferrand, France
[4] Georgian Acad Sci, Inst Pharmacochem, GE-380060 Tbilisi, Georgia
关键词
cytotoxicity; hederacolchiside A1; melanin binding; melanoma; membrane damage; high-resolution magic-angle spinning nuclear magnetic resonance; saponin;
D O I
10.1097/00008390-200404000-00004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We previously reported that hederacolchiside A1 (Hcol A1), a new oleanene saponin isolated from Hedera colchica, Koch (Araliaceae) exhibits a preferential cytotoxicity on a pigmented melanoma cell line. The present study confirms the high susceptibility of melanoma cell lines to this drug and shows concentrations producing a 50% decrease in cell content (IC50 values) inversely proportional to the melanin content of each cell line. At cytotoxic concentrations, Hcol All induces membrane-damaging effects within 6 h, cytoplasmic vacuolization within 24 h, and non-apoptotic cell death within 48 h. Using a new high-resolution magic-angle spinning nuclear magnetic resonance method, we have shown for the first time that this hederasaponin specifically interacts with melanin. The dissociation constant (2.7 mM) is comparable to those observed with drugs known to interact with melanin. Taking into consideration that the IC50 values were inversely proportional to the melanin in each cell line, our data suggest that, in addition to the delayed membrane injury induced by this drug, the ability of Hcol All to bind melanin could contribute to the higher toxicity of Hcol A1 in pigmented melanoma cells.
引用
收藏
页码:97 / 105
页数:9
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