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
引用
收藏
页数:12
相关论文
共 50 条
  • [21] 2-Thioxo-3,4-dihydropyrimidine and thiourea endowed with sulfonamide moieties as dual EGFRT790M and VEGFR-2 inhibitors: Design, synthesis, docking, and anticancer evaluations
    El-Gaby, Mohamed S. A.
    Abdel Reheim, Mohamed A. M.
    Akrim, Zuhir S. M.
    Naguib, Bassem H.
    Saleh, Nashwa M.
    El-Adasy, Abu Bakr A. A. M.
    El-Adl, Khaled
    Mohamady, Samy
    DRUG DEVELOPMENT RESEARCH, 2024, 85 (01)
  • [22] Discovery of novel thiazolyl-pyrazolines as dual EGFR and VEGFR-2 inhibitors endowed with in vitro antitumor activity towards non-small lung cancer
    Abdelsalam, Esraa A.
    Abd El-Hafeez, Amer Ali
    Eldehna, Wagdy M.
    El Hassab, Mahmoud A.
    Marzouk, Hala Mohamed M.
    Elaasser, Mahmoud M.
    Abou Taleb, Nageh A.
    Amin, Kamilia M.
    Abdel-Aziz, Hatem A.
    Ghosh, Pradipta
    Hammad, Sherif F.
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2022, 37 (01) : 2265 - 2282
  • [23] Design, synthesis, molecular docking, in silico ADMET profile and anticancer evaluations of sulfonamide endowed with hydrazone-coupled derivatives as VEGFR-2 inhibitors
    Sayed, Asmaa M.
    Taher, Fatma A.
    Abdel-Samad, Mohammad R. K.
    El-Gaby, Mohamed S. A.
    El-Adl, Khaled
    Saleh, Nashwa M.
    BIOORGANIC CHEMISTRY, 2021, 108
  • [24] Virtual Screening, Molecular Docking Studies and DFT Calculations of Novel Anticancer Flavonoids as Potential VEGFR-2 Inhibitors
    Shah, Ashish
    Parmar, Ghanshyam
    Shah, Umang
    Perumal, Sathiaseelan
    CHEMISTRY AFRICA-A JOURNAL OF THE TUNISIAN CHEMICAL SOCIETY, 2023, 6 (04): : 1847 - 1861
  • [25] Virtual Screening, Molecular Docking Studies and DFT Calculations of Novel Anticancer Flavonoids as Potential VEGFR-2 Inhibitors
    Ashish Shah
    Ghanshyam Parmar
    Umang Shah
    Sathiaseelan Perumal
    Chemistry Africa, 2023, 6 : 1847 - 1861
  • [26] A Review of Quinazoline-Based EGFR/VEGFR-2 Dual Inhibitors as Potent Anticancer Agents: Structure-Activity Relationship and Docking Studies
    Yousefbeyk, Fatemeh
    Ghasemi, Saeed
    PHARMACEUTICAL SCIENCES, 2025, 31 (01) : 43 - 64
  • [27] Design and synthesis of new 1,2,3-triazole derivatives as VEGFR-2/ telomerase downregulatory candidates endowed with apoptotic potential for cancer treatment
    Al-Karmalawy, Ahmed A.
    Zeidan, Mohamed A.
    Elmaaty, Ayman Abo
    Sharaky, Marwa
    Yassen, Asmaa S. A.
    Khaleel, Eman F.
    Eldehna, Wagdy M.
    Ashour, Heba F.
    BIOORGANIC CHEMISTRY, 2025, 156
  • [28] Concept of focused diversity: Application to development of specific and dual inhibitors of VEGFR-2 with in vivo activity.
    Kiselyov, AS
    CLINICAL CANCER RESEARCH, 2005, 11 (24) : 8966S - 8966S
  • [29] Dual VEGFR-2 and EGFRT790M inhibitors of phenyldiazenes: anticancer evaluations, ADMET, docking, design and synthesis
    Alsulaimany, Marwa
    Aljohani, Ahmed K. B.
    Abd El-Sattar, Nour E. A.
    Almadani, Sara A.
    Alatawi, Omar M.
    Alharbi, Hussam Y.
    Aljohani, Majed S.
    Al-Shareef, Adel H.
    Alghamdi, Read
    Tayeb, Saeed M.
    Keshek, Doaa E.
    El-Adl, Khaled
    Anwer, Kurls E.
    FUTURE MEDICINAL CHEMISTRY, 2025, 17 (03) : 287 - 300
  • [30] Discovery of Anilinopyrimidines as Dual Inhibitors of c-Met and VEGFR-2: Synthesis, SAR, and Cellular Activity
    Zhan, Zhengsheng
    Ai, Jing
    Liu, Qiufeng
    Ji, Yinchun
    Chen, Tiantian
    Xu, Yechun
    Geng, Meiyu
    Duan, Wenhu
    ACS MEDICINAL CHEMISTRY LETTERS, 2014, 5 (06): : 673 - 678