Investigating the Promising Anticancer Activity of Cetuximab and Fenbendazole Combination as Dual CBS and VEGFR-2 Inhibitors and Endowed with Apoptotic Potential

被引:1
|
作者
Eid, Norhan M. [1 ]
Al-Karmalawy, Ahmed A. [2 ,3 ]
Eldebss, Taha M. A. [4 ]
Elhakim, Heba K. A. [1 ]
机构
[1] Cairo Univ, Fac Sci, Biochem Div, Giza 12613, Egypt
[2] Horus Univ Egypt, Fac Pharm, Dept Pharmaceut Chem, New Damietta 34518, Egypt
[3] Ahram Canadian Univ, Fac Pharm, Pharmaceut Chem Dept, 6th October City 12566, Giza, Egypt
[4] Cairo Univ, Fac Sci, Chem Div, Giza 12613, Egypt
关键词
Cetuximab; Fenbendazole; Benzimidazole; CBS; VEGFR-2; Apoptosis; CANCER; GROWTH; CELLS; THERAPY; TARGETS; BENCH;
D O I
10.1002/cbdv.202302081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. + image
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页数:12
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