| Literature DB >> 31218441 |
Madeleine Gold1, Yusufi Mujahid2, Khursheed Ahmed2, Hana Kostrhunova3, Jana Kasparkova3,4, Viktor Brabec3, Bernhard Biersack1, Rainer Schobert5.
Abstract
2-Amino-5,10-dihydro-5,10-dioxo-4(pyridine-3-yl)-4H-benzo[g]chromene-3-carbonitrile 5, a cytotoxic lawsone derivative, was reacted with [Ru(p-cymene)Cl2]2 to afford a new Ru(II) 'piano-stool' complex 6 which differed from its ligand 5 by a greater selectivity for highly invasive 518A2 melanoma cells over human dermal fibroblasts in MTT cytotoxicity assays, and by inducing senescence rather than apoptosis in the former. DNA is a likely cellular target of complex 6 as it bound, presumably non-covalently, to linear and circular double-stranded DNA in vitro and as ruthenium was found in the lysate of nuclei of treated 518A2 melanoma cells. It also caused a fivefold increase of reactive oxygen species in these cells, originating from a more persistent redox cycling as visualised by cyclic voltammetry.Entities:
Keywords: Anticancer agents; Lawsone; Melanoma; Naphthoquinone; Ruthenium(II) complex; Senescence
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Year: 2019 PMID: 31218441 DOI: 10.1007/s00775-019-01677-y
Source DB: PubMed Journal: J Biol Inorg Chem ISSN: 0949-8257 Impact factor: 3.358