Fluorescent silver(I) and gold(I)-N-heterocyclic carbene complexes with cytotoxic properties: mechanistic insights

被引:119
|
作者
Citta, Anna [1 ]
Schuh, Esther [2 ]
Mohr, Fabian [2 ]
Folda, Alessandra [1 ]
Massimino, Maria Lina [3 ]
Bindoli, Alberto [3 ]
Casini, Angela [4 ]
Rigobello, Maria Pia [1 ]
机构
[1] Univ Padua, Dipartimento Sci Biomed, I-35131 Padua, Italy
[2] Berg Univ Wuppertal, Fachbereich C, D-42119 Wuppertal, Germany
[3] Ist Neurosci CNR, Sez Padova, Dipartimento Sci Biomed, I-35131 Padua, Italy
[4] Univ Groningen, Res Inst Pharm, NL-9713 AV Groningen, Netherlands
关键词
THIOREDOXIN REDUCTASE; GOLD(I) COMPLEXES; IN-VITRO; STRUCTURAL-CHARACTERIZATION; ANTICANCER THERAPEUTICS; CANCER-CELLS; AGENTS; OXIDATION; APOPTOSIS; GLUTATHIONE;
D O I
10.1039/c3mt20260g
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Silver(I) and gold(I)-N-heterocyclic carbene (NHC) complexes bearing a fluorescent anthracenyl ligand were examined for cytotoxicity in normal and tumor cells. The silver(I) complex exhibits greater cytotoxicity in tumor cells compared with normal cells. Notably, in cell extracts, this complex determines a more pronounced inhibition of thioredoxin reductase (TrxR), but it is ineffective towards glutathione reductase (GR). Both gold and silver complexes lead to oxidation of the thioredoxin system, the silver(I) derivative being particularly effective. In addition, the dimerization of peroxiredoxin 3 (Prx3) was also observed, demonstrating the ability of these compounds to reach the mitochondrial target. The fluorescence microscopy visualization of the subcellular distribution of the complexes shows a larger diffusion of these molecules in tumor cells with respect to normal cells.
引用
收藏
页码:1006 / 1015
页数:10
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