Publication

Oxidative stress induced by Pt(IV) pro-drugs based on the cisplatin scaffold and indole carboxylic acids in axial position

Tolan, Dina
Gandin, Valentina
Morrison, Liam
El-Nahas, Ahmed
Marzano, Cristina
Montagner, Diego
Erxleben, Andrea
Citation
Tolan, Dina, Gandin, Valentina, Morrison, Liam, El-Nahas, Ahmed, Marzano, Cristina, Montagner, Diego, & Erxleben, Andrea. (2016). Oxidative Stress Induced by Pt(IV) Pro-drugs Based on the Cisplatin Scaffold and Indole Carboxylic Acids in Axial Position. Scientific Reports, 6, 29367. doi: 10.1038/srep29367 https://www.nature.com/articles/srep29367#supplementary-information
Abstract
The use of Pt(IV) complexes as pro-drugs that are activated by intracellular reduction is a widely investigated approach to overcome the limitations of Pt(II) anticancer agents. A series of ten mono- and bis-carboxylated Pt(IV) complexes with axial indole-3-acetic acid (IAA) and indole-3-propionic acid (IPA) ligands were synthesized and characterized by elemental analysis, ESI-MS, FT-IR, H-1 and Pt-195 NMR spectroscopy. Cellular uptake, DNA platination and cytotoxicity against a panel of human tumor cell lines were evaluated. All the complexes are able to overcome cisplatin-resistance and the most potent complex, cis, cis, trans-[Pt(NH3)(2)Cl-2(IPA)(OH)] was on average three times more active than cisplatin. Mechanistic studies revealed that the trend in cytotoxicity of the Pt(IV) complexes is primarily consistent with their ability to accumulate into cancer cells and to increase intracellular basal reactive oxygen species levels, which in turn results in the loss of mitochondrial membrane potential and apoptosis induction. The role of the indole acid ligand as a redox modulator is discussed.
Funder
Publisher
Nature Publishing Group
Publisher DOI
10.1038/srep29367
Rights
Attribution-NonCommercial-NoDerivs 3.0 Ireland