An adsorptive transfer technique coupled with brdicka reaction to reveal the importance of metallothionein in chemotherapy with platinum based cytostatics
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21614176
PubMed Central
PMC3100849
DOI
10.3390/ijms11124826
PII: ijms11124826
Knihovny.cz E-zdroje
- Klíčová slova
- anticancer therapy, metallothionein, platinum based anticancer drugs, resistance, retinoblastoma, tumor disease,
- MeSH
- antitumorózní látky * farmakokinetika farmakologie MeSH
- biologické modely MeSH
- cisplatina * farmakokinetika farmakologie MeSH
- karboplatina * farmakokinetika farmakologie MeSH
- králíci MeSH
- lidé MeSH
- metalothionein metabolismus MeSH
- nádorové buněčné linie MeSH
- neuroblastom * farmakoterapie metabolismus patologie MeSH
- retinoblastom * farmakoterapie metabolismus patologie MeSH
- zvířata MeSH
- Check Tag
- králíci MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antitumorózní látky * MeSH
- cisplatina * MeSH
- karboplatina * MeSH
- metalothionein MeSH
The drugs based on platinum metals represent one of the oldest, but also one of the most effective groups of chemotherapeutic agents. Thanks to many clinical studies it is known that resistance of tumor cells to drugs is a frequent cause of chemotherapy failure. With regard to platinum based drugs, multidrug resistance can also be connected with increased expression of low-molecular weight protein metallothionein (MT). This study aimed at investigating the interactions of MT with cisplatin or carboplatin, using the adsorptive transfer technique coupled with differential pulse voltammetry Brdicka reaction (AdTS DPV Brdicka reaction), and a comparison of in vitro results with results obtained in vivo. The results obtained from the in vitro study show a strong affinity between platinum based drugs and MT. Further, we analyzed extracts of neuroblastoma cell lines treated with cisplatin or carboplatin. It is clear that neuroblastoma UKF-NB-4 cisplatin-resistant and cisplatin-sensitive cell lines unlikely respond to the presence of the platinum-based cytostatics cisplatin and carboplatin. Finally, we determined the level of MT in samples from rabbits treated with carboplatin and patients with retinoblastoma treated with the same drug.
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