Login / Signup

In Vitro and In Vivo Biological Activities of Dipicolinate Oxovanadium(IV) Complexes.

Katarzyna CzerwińskaBeatriz FilipeAnna ŚwitlickaMateusz PenkalaBarbara MachuraAlina BieńkoSandra CordeiroPedro Viana BaptistaAlexandra Ramos Fernandes
Published in: Journal of medicinal chemistry (2023)
The work is focused on anticancer properties of dipicolinate (dipic)-based vanadium(IV) complexes [VO(dipic)(N ∩ N)] bearing different diimines (2-(1 H -imidazol-2-yl)pyridine, 2-(2-pyridyl)benzimidazole, 1,10-phenanthroline-5,6-dione, 1,10-phenanthroline, and 2,2'-bipyridine), as well as differently 4,7-substituted 1,10-phenanthrolines. The antiproliferative effect of V(IV) systems was analyzed in different tumors (A2780, HCT116, and HCT116-DoxR) and normal (primary human dermal fibroblasts) cell lines, revealing a high cytotoxic effect of [VO(dipic)(N ∩ N)] with 4,7-dimethoxy-phen ( 5 ), 4,7-diphenyl-phen ( 6 ), and 1,10-phenanthroline ( 8 ) against HCT116-DoxR cells. The cytotoxicity differences between these complexes can be correlated with their different internalization by HCT116-DoxR cells. Worthy of note, these three complexes were found to (i) induce cell death through apoptosis and autophagy pathways, namely, through ROS production; (ii) not to be cytostatic; (iii) to interact with the BSA protein; (iv) do not promote tumor cell migration or a pro-angiogenic capability; (v) show a slight in vivo anti-angiogenic capability, and (vi) do not show in vivo toxicity in a chicken embryo.
Keyphrases
  • cell cycle arrest
  • cell death
  • cell migration
  • pi k akt
  • molecular docking
  • endothelial cells
  • oxidative stress
  • endoplasmic reticulum stress
  • pregnant women
  • induced pluripotent stem cells