Počet záznamů: 1  

The Gold(I) Complex with Plant Hormone Kinetin Shows Promising In Vitro Anticancer and PPARγ Properties

  1. 1.
    SYSNO ASEP0571095
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevThe Gold(I) Complex with Plant Hormone Kinetin Shows Promising In Vitro Anticancer and PPARγ Properties
    Tvůrce(i) Trávníček, Z. (CZ)
    Vančo, J. (CZ)
    Belza, J. (CZ)
    Hošek, J. (CZ)
    Dvořák, Z. (CZ)
    Lenobel, René (UEB-Q) ORCID
    Popa, I. (CZ)
    Šmejkal, K. (CZ)
    Uhrin, P. (AT)
    Celkový počet autorů9
    Číslo článku2293
    Zdroj.dok.International Journal of Molecular Sciences. - : MDPI
    Roč. 24, č. 3 (2023)
    Poč.str.21 s.
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovaanti-inflammatory ; anticancer ; apoptosis ; cell cycle ; gold(I) complex ; in vitro ; kinetin ; ppar ; ros
    Obor OECDPhysical chemistry
    Způsob publikováníOpen access
    Institucionální podporaUEB-Q - RVO:61389030
    UT WOS000930771000001
    EID SCOPUS85148045447
    DOI10.3390/ijms24032293
    AnotaceMotivated by the clinical success of gold(I) metallotherapeutic Auranofin in the effective treatment of both inflammatory and cancer diseases, we decided to prepare, characterize, and further study the [Au(kin)(PPh3)] complex (1), where Hkin = kinetin, 6-furfuryladenine, for its in vitro anti-cancer and anti-inflammatory activities. The results revealed that the complex (1) had significant in vitro cytotoxicity against human cancer cell lines (A2780, A2780R, PC-3, 22Rv1, and THP-1), with IC50 ≈ 1–5 μM, which was even significantly better than that for the conventional platinum-based drug Cisplatin while comparable with Auranofin. Although its ability to inhibit transcription factor NF-κB activity did not exceed the comparative drug Auranofin, it has been found that it is able to positively influence peroxisome-proliferator-activated receptor-gamma (PPARγ), and as a consequence of this to have the impact of moderating/reducing inflammation. The cellular effects of the complex (1) in A2780 cancer cells were also investigated by cell cycle analysis, induction of apoptosis, intracellular ROS production, activation of caspases 3/7 and disruption of mitochondrial membrane potential, and shotgun proteomic analysis. Proteomic analysis of R2780 cells treated with complex (1) and starting compounds revealed possible different places of the effect of the studied compounds. Moreover, the time-dependent cellular accumulation of copper was studied by means of the mass spectrometry study with the aim of exploring the possible mechanisms responsible for its biological effects.
    PracovištěÚstav experimentální botaniky
    KontaktDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Rok sběru2024
    Elektronická adresahttps://doi.org/10.3390/ijms24032293
Počet záznamů: 1  

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