Pregled bibliografske jedinice broj: 1011016
Pd(II) complexes with N-heteroaromatic hydrazone ligands: Anticancer activity, in silico and experimental target identification
Pd(II) complexes with N-heteroaromatic hydrazone ligands: Anticancer activity, in silico and experimental target identification // Journal of inorganic biochemistry, 199 (2019), 110758, 18 doi:10.1016/j.jinorgbio.2019.110758 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1011016 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Pd(II) complexes with N-heteroaromatic hydrazone ligands: Anticancer activity, in silico and experimental target identification
Autori
Bjelogrlić, Snežana K. ; Todorović, Tamara R. ; Kojić, Milan ; Senćanski, Milan ; Nikolić, Milan ; Višnjevac, Aleksandar ; Araškov, Jovana ; Miljković, Marija ; Mueller, Christian D. ; Filipović, Nenad R.
Izvornik
Journal of inorganic biochemistry (0162-0134) 199
(2019);
110758, 18
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Pd(II)complexes ; Hydrazones ; Apoptosis ; Topoisomerase inhibition ; DNAinteractions ; HSAinteractions
(Hydrazones ; Apoptosis ; Topoisomerase inhibition ; DNAinteractions ; HSAinteractions)
Sažetak
Anticancer activity of Pd complexes 1–5 with bidentate N-heteroaromatic hydrazone ligands was investigated on human acute monocytic leukemia (THP-1 ; cells in a suspension) and human mammary adenocarcinoma (MCF-7 ; two-dimensional layer and three-dimensional spheroid tumor model) cell lines. For the Pd(II) complexes with condensation products of ethyl hydrazainoacetate and quinoline-8-carboxaldehyde (complex 1) and 2-formylpyridine (complex 3), for which apoptosis was determined as a mechanism of anticancer activity, further investigation revealed that they arrest the cell cycle in G0/G1 phase, induce generation of reactive oxygen species and inhibit Topoisomerase I in vitro. In silico studies corroborate experimental findings that these complexes show topoisomerase inhibition activity in the micromolar range and indicate binding to a DNA's minor groove as another potential target. Based on the results obtained by circular dichroism and fluorescence spectroscopy measurements, the most active complexes are suitable to be delivered to a blood stream via human serum albumin.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE