Targeting EGFR and VEGFR-2 Kinases With Nanoparticles: A Computational Approach for Cancer Therapy Advancement.
Ibrahim KhaterAaya M NassarPublished in: Cancer investigation (2024)
The study investigates titanium and zinc nanoparticles as inhibitors for the epidermal growth factor receptor (EGFR) and vascular endothelial growth factor receptor-2 (VEGFR-2), pivotal regulators of cell processes. VEGFR-2 activation fuels tumor angiogenesis in cancer cells, sustaining malignant tissue expansion. Molecular docking analysis illustrates the nanoparticles' binding to the active sites, inhibiting the phosphorylation of key proteins in downstream signaling. This inhibition offers a promising therapeutic approach to impede cancer-related signaling, potentially slowing down aberrant protein cascades controlled by EGFR and VEGFR-2. The findings propose a novel avenue for cancer treatment, targeting abnormal growth pathways using titanium and zinc nanoparticles.
Keyphrases
- vascular endothelial growth factor
- epidermal growth factor receptor
- cancer therapy
- molecular docking
- tyrosine kinase
- advanced non small cell lung cancer
- endothelial cells
- small cell lung cancer
- drug delivery
- molecular dynamics simulations
- single cell
- walled carbon nanotubes
- binding protein
- stem cells
- protein protein
- mesenchymal stem cells
- bone marrow
- amino acid