Study of Interactions between Metallothionein and Cisplatin by using Differential Pulse Voltammetry Brdickás reaction and Quartz Crystal Microbalance.

Citation data:

Sensors (Basel, Switzerland), ISSN: 1424-8220, Vol: 9, Issue: 3, Page: 1355-69

Publication Year:
2009
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Repository URL:
http://publikace.k.utb.cz/handle/10563/1001701; https://dspace.vutbr.cz/xmlui/handle/11012/70083; http://hdl.handle.net/10563/1001701
PMID:
22573958
DOI:
10.3390/s90301355
PMCID:
PMC3345864; 3345864
Author(s):
Húska, Dalibor; Fabrik, Ivo; Baloun, Jiří; Adam, Vojtěch; Masařík, Michal; Hubálek, Jaromír; Vašků, Anna; Trnková, Libuše; Horna, Aleš; Zeman, Ladislav; Kizek, Roman Show More Hide
Publisher(s):
MDPI AG; Molecular Diversity Preservation International (MDPI)
Tags:
Chemistry; Physics and Astronomy; Biochemistry, Genetics and Molecular Biology; Engineering; Cancer; Metallothionein; Cisplatin; Protein-Drug Interaction; Voltammetry; Brdicka's reaction; Quartz Crystal Microbalance
article description
Treatment strategies for tumour diseases are progressively focusing on personalization of medicine. However, this focus requires methods revealing the early general biological mechanisms, including the formation anti-cancer drugs' resistance. The low molecular mass protein metallothionein is thought to be the crucial for the formation of resistance in tumour treatment based on the platinum-cytostatics. The interactions between metallothionein (MT) and cisplatin were determined by the adsorptive transfer stripping technique coupled with the differential pulse votlammetry Brdickás reaction. The signals related to the MT-cisplatin complex appeared at -0.9 V. The formation of this complex depended on the time of interaction between cisplatin and MT. The complex formation was consequently confirmed by quartz crystal microbalance analyses. The formation of this complex was detectable even after a 20 s long interaction. Moreover, we detected presence of MT-cisplatin complex in the blood of male rats treated with this drug.