Biological study of the effect of water soluble [N-(2-hydroxybenzyl)-l-aspartato] gallium complexes on breast carcinoma and fibrosarcoma cells

Abstract

© 2016, SBIC. Abstract: Two water soluble gallium complexes described as [Ga(III)LCl], where l is the deprotonated form of N-2-hydroxybenzyl aspartic acid derivatives, were synthesized and characterized by1H NMR,13C NMR, FT-IR, mass spectrometry, and elemental analysis. The 2-(5-chloro-2-hydroxybenzylamino)succinic acid derivative (GS2) has been found to be a promising anticancer drug candidate. This compound was found to be more cytotoxic against human breast carcinoma MDA-MB231 and fibrosarcoma HT-1080 cell lines than the unsubstituted derivative and GaCl3. GS2 was able to induce apoptosis through downregulation of AKT phosphorylation, G2M arrest in cell cycle, and caspase 3/7 pathway. This gallium complex was found to induce an increase in mitochondrial ROS level in HT-1080 cells but not in MDA-MB231 cells. This suggests that the mechanism of action of GS2 would not be mediated by the drug-induced oxidative stress but probably by directly and indirectly inhibiting the AKT cell-signaling pathway. Graphical abstract: [Figure not available: see fulltext.]