Cytotoxic and apoptotic effects of ternary silver(i) complexes bearing 2-formylpyridine thiosemicarbazones and 1,10-phenanthroline.
Débora Eduarda Soares SilvaAmanda B BecceneriMariana C SolciaJoão V B SantiagoMariete B MoreiraJosé A Gomes NetoFernando R PavanMarcia Regina CominettiJosé C M PereiraAdelino V G NettoPublished in: Dalton transactions (Cambridge, England : 2003) (2020)
New silver(i) compounds containing 2-formylpyridine-N(4)-R-thiosemicarbazones and 1,10-phenanthroline (phen) were synthesized and characterized by spectroscopic techniques (IR and NMR), elemental analysis, ESI-MS and molar conductance measurements. In these complexes, both phen and thiosemicarbazone ligands are coordinated in a chelating bidentate fashion. Compounds 1-3 not only showed good in vitro antiproliferative activity against human lung (A549) and breast tumor cells (MDA-MB-231 and MCF-7), with IC50 values ranging from 1.49 to 20.90 μM, but were also demonstrated to be less toxic towards human breast non-tumor cells (MCF-10A). Cellular uptake studies indicated that compounds 1-3 were taken up by the MDA-MB-231 cells in 6 hours. Cell death assays in the MDA-MB-231 cells were conducted with compound 1 aiming to evaluate its effects on cell morphology, induction of apoptosis, the cell cycle, reactive oxygen species (ROS) formation and mitochondrial membrane potential (Δψm). Compound 1 caused morphological changes, such as cell shrinkage and rounding, increased the sub-G1 phase population, and induced apoptotic cell death, ROS formation and loss of mitochondrial membrane potential (Δψm). DNA binding results revealed that 1 interacted with the ct-DNA minor groove. Complexes 1-3 also exhibited good in vitro activity against M. tuberculosis H37Rv, with MIC values ranging from 3.37 to 4.65 μM.
Keyphrases
- cell death
- cell cycle arrest
- cell cycle
- dna binding
- single cell
- breast cancer cells
- reactive oxygen species
- mycobacterium tuberculosis
- ms ms
- gold nanoparticles
- oxidative stress
- cell proliferation
- cell therapy
- multiple sclerosis
- endothelial cells
- magnetic resonance
- transcription factor
- pi k akt
- mass spectrometry
- computed tomography
- induced apoptosis
- high throughput
- molecular docking
- high glucose
- silver nanoparticles
- hiv aids
- dna damage
- stem cells
- bone marrow
- contrast enhanced
- signaling pathway
- induced pluripotent stem cells
- dual energy
- electronic health record
- anti inflammatory
- mesenchymal stem cells
- solid state