Effects of cytotoxic cis- and trans-diammine monochlorido platinum(II) complexes on selenium-dependent redox enzymes and DNA

0486052 - BFÚ 2018 RIV US eng J - Článek v odborném periodiku
Lemmerhirt, H. - Behnisch, S. - Bodtke, A. - Lillig, Ch.H. - Pazderová, L. - Kašpárková, Jana - Brabec, Viktor - Bednarski, P.J.
Effects of cytotoxic cis- and trans-diammine monochlorido platinum(II) complexes on selenium-dependent redox enzymes and DNA.
Journal of Inorganic Biochemistry. Roč. 178, JAN2018 (2018), s. 94-105. ISSN 0162-0134. E-ISSN 1873-3344
Grant CEP: GA ČR GA17-09436S
Institucionální podpora: RVO:68081707
Klíčová slova: glutathione-peroxidase * thioredoxin reductase
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 3.224, rok: 2018

Here we present the preparation of 14 pairs of cis-and trans-diammine monochlorido platinum(II) complexes, coordinated to heterocycles (i.e., imidazole, 2-methylimidazole and pyrazole) and linked to various acylhydrazones, which were designed as potential inhibitors of the selenium-dependent enzymes glutathione peroxidase 1 (GPx-1) and thioredoxin reductase 1 (TrxR-1). However, no inhibition of bovine GPx-1 and only weak inhibition of murine TrxR-1 was observed in in vitro assays. Nonetheless, the cis configured diammine monochlorido Pt(II) complexes exhibited cytotoxic and apoptotic properties on various human cancer cell lines, whereas the trans configured complexes generally showed weaker potency with a few exceptions. On the other hand, the trans complexes were generally more likely to lack cross-resistance to cisplatin than the cis analogues. Platinum was found bound to the nuclear DNA of cancer cells treated with representative Pt complexes, suggesting that DNA might be a possible target. Thus, detailed in vitro binding experiments with DNA were conducted. Interactions of the compounds with calf thymus DNA were investigated, including Pt binding kinetics, circular dichroism (CD) spectral changes, changes in DNA melting temperatures, unwinding of supercoiled plasmids and ethidium bromide displacement in DNA. The CD results indicate that the most active cis configured pyrazole-derived complex causes unique structural changes in the DNA compared to the other complexes as well as to those caused by cisplatin, suggesting a denaturation of the DNA structure. This may be important for the antiproliferative activity of this compound in the cancer cells.
Trvalý link: http://hdl.handle.net/11104/0280940