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Chem Biodivers ; 21(4): e202302081, 2024 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-38318954

RESUMO

In this work, the cytotoxicity of monoclonal antibody (Cetuximab, Ce) and Fenbendazole (Fen), as well as their combination therapy were tested with the MTT assay. On the other side, Ce, Fen, and a combination between them were subjected to a colchicine-tubulin binding test, which was conducted and compared to Colchicine as a reference standard. Besides, Ce, Fen, and the combination of them were tested against the VEGFR-2 target receptor, compared to Sorafenib as the standard medication. Moreover, the qRT-PCR technique was used to investigate the levels of apoptotic genes (p53 and Bax) and anti-apoptotic gene (Bcl-2) as well. Also, the effect of Ce, Fen, and the combination of them on the level of ROS was studied. Furthermore, the cell cycle analysis and Annexin V apoptosis assay were carried out for Ce, Fen, and a combination of them. In addition, the molecular docking studies were used to describe the molecular levels of interactions for both (Fen and colchicine) or (Fen and sorafenib) within the binding pockets of the colchicine binding site (CBS) and vascular endothelial growth factor-2 receptor (VEGFR-2), respectively.


Assuntos
Antineoplásicos , Cetuximab/farmacologia , Antineoplásicos/farmacologia , Antineoplásicos/química , Receptor 2 de Fatores de Crescimento do Endotélio Vascular , Fenbendazol/farmacologia , Simulação de Acoplamento Molecular , Sorafenibe/farmacologia , Fator A de Crescimento do Endotélio Vascular/farmacologia , Proliferação de Células , Sítios de Ligação , Receptores de Fatores de Crescimento do Endotélio Vascular , Apoptose , Colchicina/farmacologia , Relação Estrutura-Atividade , Inibidores de Proteínas Quinases/química , Estrutura Molecular , Ensaios de Seleção de Medicamentos Antitumorais
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