Therapeutic Potential of 2,2′:6′,2″-Terpyridine-Based Au(III), Pt(II), and Mn(II) Complexes against 2D and 3D Human Colorectal Resistant Cancer Cells
作者
Katarzyna Choroba,B. Machura,Mateusz Penkala,Karol Erfurt,Sandra Cordeiro,Vanessa Souza Araújo,Edvânia Leopoldo,Regina Aparecida Garcia de Lima,Diogo Afonso,Pedro V. Baptista,Alexandra R. Fernandes
The antiproliferative effect of [AuCl(tmp-terpy)](PF6)2 (1), [PtCl(tmp-terpy)](CF3SO3) (2), [MnCl2(tmp-terpy)] (3), and 4'-(3,4,5-trimethoxy-phenyl)-2,2':6',2″-terpyridine (tmp-terpy) was analyzed in sensitive and doxorubicin-resistant (DoxR) colorectal cancer (CRC) cell lines and in normal primary human fibroblasts. Comprehensive studies were performed for 1 and tmp-terpy, showing the strongest cytotoxicity in HCT116DoxR 2D cells and having the capability to induce the loss of cell viability in 3D HCT116DoxR spheroids. Complex 1 internalizes CRC-resistant cancer cells and increases the number of reactive oxygen species (ROS), triggering cell death by apoptosis and autophagy. Changes in protein expression levels of HCT116DoxR cells exposed to 1 and tmp-terpy primarily affect protein folding, apoptosis, and stress response, consistent with the observed induction of programmed cell death and ROS. The combination of 1 or tmp-terpy with oxaliplatin (OX) and cisplatin (Cis) shows cytotoxic effects in 3D CRC-resistant spheroids. No in vivo toxicity in a chicken embryo is observed, even when 1 is combined with an OX and Cis.