Bioactive Tryptophan-Based Copper Complex with Auxiliary β-Carboline Spectacle Potential on Human Breast Cancer Cells: In Vitro and In Vivo Studies.
Walaa AlharbiIftekhar HassanRais Ahmad KhanShazia ParveenKhadijah H AlharbiIbtisam I Bin SharfanIbrahim M AlhazzaHossam EbaidAli M AlsalmePublished in: Molecules (Basel, Switzerland) (2021)
Biocompatible tryptophan-derived copper (1) and zinc (2) complexes with norharmane (β-carboline) were designed, synthesized, characterized, and evaluated for the potential anticancer activity in vitro and in vivo. The in vitro cytotoxicity of both complexes 1 and 2 were assessed against two cancerous cells: (human breast cancer) MCF7 and (liver hepatocellular cancer) HepG2 cells with a non-tumorigenic: (human embryonic kidney) HEK293 cells. The results exhibited a potentially decent selectivity of 1 against MCF7 cells with an IC50 value of 7.8 ± 0.4 μM compared to 2 (less active, IC50 ~ 20 μM). Furthermore, we analyzed the level of glutathione, lipid peroxidation, and visualized ROS generation to get an insight into the mechanistic pathway and witnessed oxidative stress. These in vitro results were ascertained by in vivo experiments, which also supported the free radical-mediated oxidative stress. The comet assay confirmed the oxidative stress that leads to DNA damage. The histopathology of the liver also ascertained the low toxicity of 1.
Keyphrases
- oxidative stress
- induced apoptosis
- dna damage
- breast cancer cells
- endothelial cells
- cell cycle arrest
- endoplasmic reticulum stress
- signaling pathway
- cell death
- oxide nanoparticles
- induced pluripotent stem cells
- ischemia reperfusion injury
- pluripotent stem cells
- diabetic rats
- dna repair
- young adults
- high throughput
- squamous cell
- structural basis