| Literature DB >> 18702458 |
Tijana Bugarcic1, Olga Nováková, Anna Halámiková, Lenka Zerzánková, Oldrich Vrána, Jana Kaspárková, Abraha Habtemariam, Simon Parsons, Peter J Sadler, Viktor Brabec.
Abstract
We have compared the cancer cell cytotoxicity, cell uptake, and DNA binding properties of the isomeric terphenyl complexes [(eta(6)-arene)Ru(en)Cl](+), where the arene is ortho- (2), meta- (3), or para-terphenyl (1) (o-, m-, or p-terp). Complex 1, the X-ray crystal structure of which confirms that it has the classical "piano-stool" geometry, has a similar potency to cisplatin but is not cross-resistant and has a much higher activity than 2 or 3. The extent of Ru uptake into A2780 or A2780cis cells does not correlate with potency. Complex 1 binds to DNA rapidly and quantitatively, preferentially to guanine residues, and causes significant DNA unwinding. Circular and linear dichroism, competitive binding experiments with ethidium bromide, DNA melting, and surface-enhanced Raman spectroscopic data are consistent with combined intercalative and monofunctional (coordination) binding mode of complex 1. This unusual DNA binding mode may therefore make a major contribution to the high potency of complex 1.Entities:
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Year: 2008 PMID: 18702458 DOI: 10.1021/jm8003043
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446