Issue 24, 2014

Structural characterization and biological evaluation of a clioquinol–ruthenium complex with copper-independent antileukaemic activity

Abstract

In this study, we present the synthesis, biological characterization, and first crystal structure of an organometallic–clioquinol complex. Combining ruthenium with the established apoptotic agent and 8-hydroxyquinoline derivative, clioquinol, resulted in a complex that induces caspase-dependent cell death in leukaemia cells. This activity is copper independent and is improved compared to the parent compound, clioquinol. The study of the mode of action reveals that this clioquinol–ruthenium complex does not intercalate between DNA base pairs. Additionally, this clioquinol–ruthenium complex shows proteasome-independent inhibition of the NFκB signalling pathway, with no effects on cell-cycle distribution. These data suggest a mechanism of action that involves a target profile that is different from that for clioquinol alone.

Graphical abstract: Structural characterization and biological evaluation of a clioquinol–ruthenium complex with copper-independent antileukaemic activity

Supplementary files

Article information

Article type
Paper
Submitted
13 Feb 2014
Accepted
04 Apr 2014
First published
04 Apr 2014
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2014,43, 9045-9051

Author version available

Structural characterization and biological evaluation of a clioquinol–ruthenium complex with copper-independent antileukaemic activity

M. Gobec, J. Kljun, I. Sosič, I. Mlinarič-Raščan, M. Uršič, S. Gobec and I. Turel, Dalton Trans., 2014, 43, 9045 DOI: 10.1039/C4DT00463A

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