Anti-cancer effects of wedelolactone: interactions with copper and subcellular localization. Issue 10 (21st September 2018)

• Record Type: Journal Article
• Authors: Kučírková, Tereza; Stiborek, Marek; Dúcka, Monika; Navrátilová, Jarmila; Bogdanović Pristov, Jelena; Popović-Bijelić, Ana; Vojvodić, Snežana; Preisler, Jan; Kanický, Viktor; Šmarda, Jan; Spasojević, Ivan; Beneš, Petr
• Is Part Of: Metallomics. Volume 10:Issue 10(2018)
• Page Start: 1524
• Page End: 1531
• Publication Date: 2018-09-21
• Subjects: Metals -- Physiological effect -- Periodicals; 572.51
• DOI: 10.1039/c8mt00191j
• Languages: English
• ISSNs: 1756-5901

Abstract

Abstract : Wedelactone forms a 2 : 1 coordination complex with Cu 2+ in cancer cells to exert cytotoxic effects. Abstract : Wedelactone (WL), a plant polyphenolic derivative of coumestan, represents a promising anti-cancer agent. The underlying mechanisms of its action are not fully understood and appear to involve interplay with copper ions. Herein, we examined coordination and redox interactions of WL with Cu 2+ in phosphate buffer (pH 7), and in two breast cancer cell lines. EPR, UV-Vis and fluorescence spectroscopy showed that WL and Cu 2+ build a coordination complex with 2 : 1 stoichiometry and distorted tetrahedral geometry. WL showed strong fluorescence that was quenched by Cu 2+ . The sequestration of the intracellular copper pool with neocuproine led to a significant drop in the cytotoxic effects of WL, whereas the co-application of Cu 2+ and WL and the formation of an extracellular complex suppressed both the cytotoxic effects of WL and copper loading. Fluorescence microscopy showed that WL is mainly localized in the cytosol and significantly less in the nuclei. WL fluorescence was stronger in cells pretreated with neocuproine, implying that the complex of WL and Cu 2+ is formed inside the cells. WL caused a two-fold increase in the lysosomal level of copper as well as copper-dependent lysosome membrane permeabilization. On the other hand, the protective effects of overexpression of thioredoxin 1 imply that WL exerts the main oxidative impact inside the nucleus. The interactions of WL with copper may be essential for therapeutic performance and selectivity against cancer cells, taking into account that a number of cancer types, including breast cancer, exhibit increased intratumoral copper levels or altered copper distribution.