Synthesis, Molecular Docking, and Anticancer Screening of Ester-based Thiazole Derivatives

被引:0
作者
Musa, Mustapha [1 ,2 ]
Bello, Muhammadu [2 ]
Agwamba, Ernest C. [3 ,4 ]
机构
[1] Univ Nottingham, GSK Carbon Neutral Labs Sustainable Chem, Triumph Rd, Nottingham NG7 2TU, England
[2] Shehu Shagari Coll Educ, Dept Chem, Sokoto, Sokoto State, Nigeria
[3] Univ Calabar, Computat & Biosimulat Res Grp, Calabar, Nigeria
[4] Covenant Univ, Dept Chem, Ota, Nigeria
关键词
Anticancer; Docking; Synthesis; Biological studies; Cyclisation; MODELS; POTENT; ANTIBACTERIAL; ACTIVATION; INHIBITORS; BENZAMIDES; DISCOVERY; APOPTOSIS; DESIGN; TRAIL;
D O I
10.1002/cbdv.202401159
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
This study investigates the potential of five compounds as novel anticancer agents. We examined their efficacy, mechanisms of action, and impact on various cancer cell lines, through a comprehensive set of experiments. Notably, compound 3e demonstrated superior activity compared to the positive control cisplatin, with a GI50 value of 6.3 +/- 0.7 mu M against the breast cancer cell line (MCF-7). Compound 3b also displayed remarkable growth inhibition, yielding GI50 values of 8.7 +/- 0.2 mu M (MCF-7) and 8.9 +/- 0.5 mu M against the colon cancer cell line (HCT-116). Cell count experiments further confirmed the potent inhibitory effects of compounds 3e, 3b, and 3c on MCF-7 and HCT-116 cell growth. Compound 3e demonstrated a reduction of 55-60 % at GI50 and complete inhibition (100 %) at 2x GI50. Compound 3b exhibited 50-55 % reduction (GI50) and 90-95 % inhibition (2x GI50) in HCT-116 cells. Compound 3c displayed 75-80 % inhibition (2x GI50) and 35-40 % inhibition (GI50) in HCT-116 cells. In-depth mechanistic investigations unveiled valuable insights into the mode of action of compound 3e. The cell-cycle assay demonstrated G2/M phase arrest, DNA damage, and caspase-mediated apoptosis in both MCF-7 and HCT-116 cells. Caspase activation indicated a significant increase in apoptosis following exposure to compound 3e. Furthermore, compound 3e induced reactive oxygen species (ROS) production, influencing HCT-116 and MCF-7 cells differently. Elevated ROS production in HCT-116 cells and distinct effects in MCF-7 cells contribute to a deeper understanding of the cytotoxic mechanisms of compound 3e. Overall, these findings highlight the potential of the investigated compounds, particularly compound 3e, as effective inducers of apoptosis in cancer cells. Mechanistic insights into cell cycle arrest, caspase-mediated apoptosis, and ROS modulation provide a comprehensive understanding of their cytotoxic effects. This study offers significant contribution to the development of promising anticancer agents and their therapeutic applications. image
引用
收藏
页数:17
相关论文
共 83 条
  • [71] Benzothiazole Derivatives as Potential Anti-Infective Agents
    Sharma, Prabodh Chander
    Bansal, Kushal Kumar
    Deep, Aakash
    Pathak, Meenakshi
    [J]. CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2017, 17 (02) : 208 - 237
  • [72] Synthesis and reactivity of spiro-fused β-lactams
    Singh, Girija S.
    D'hooghe, Matthias
    De Kimpe, Norbert
    [J]. TETRAHEDRON, 2011, 67 (11) : 1989 - 2012
  • [73] Inhibition of multiple CDKs potentiates colon cancer chemotherapy via p73-mediated DR5 induction
    Tong, Jingshan
    Tan, Xiao
    Hao, Suisui
    Ermine, Kaylee
    Lu, Xinyan
    Liu, Zhaojin
    Jha, Anupma
    Yu, Jian
    Zhang, Lin
    [J]. ONCOGENE, 2023, 42 (12) : 869 - 880
  • [74] Vasu N., 2013, Rasayan J. Chem, V6, P201
  • [75] Tumor Necrosis Factor-related Apoptosis-inducing Ligand (TRAIL) Protein-induced Lysosomal Translocation of Proapoptotic Effectors Is Mediated by Phosphofurin Acidic Cluster Sorting Protein-2 (PACS-2)
    Werneburg, Nathan W.
    Bronk, Steve F.
    Guicciardi, Maria Eugenia
    Thomas, Laurel
    Dikeakos, Jimmy D.
    Thomas, Gary
    Gores, Gregory J.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (29) : 24427 - 24437
  • [76] A detailed view of a ribosomal active site: The structure of the L11-RNA complex
    Wimberly, BT
    Guymon, R
    McCutcheon, JP
    White, SW
    Ramakrishnan, V
    [J]. CELL, 1999, 97 (04) : 491 - 502
  • [77] Comparative genomic and protein sequence analyses of a complex system controlling bacterial chemotaxis
    Wuichet, Kristin
    Alexander, Roger P.
    Zhulin, Igor B.
    [J]. TWO-COMPONENT SIGNALING SYSTEMS, PT A, 2007, 422 : 3 - 31
  • [78] Regulation of estrogen signaling and breast cancer proliferation by an ubiquitin ligase TRIM56
    Xue, Min
    Zhang, Kai
    Mu, Kun
    Xu, Juntao
    Yang, Huijie
    Liu, Yun
    Wang, Beibei
    Wang, Zhonghao
    Li, Zhongbo
    Kong, Qiong
    Li, Xiumin
    Wang, Hui
    Zhu, Jian
    Zhuang, Ting
    [J]. ONCOGENESIS, 2019, 8 (5)
  • [79] Amphiphilic Poly(N-vinylpyrrolidone) Nanoparticles Conjugated with DR5-Specific Antitumor Cytokine DR5-B for Targeted Delivery to Cancer Cells
    Yagolovich, Anne
    Kuskov, Andrey
    Kulikov, Pavel
    Kurbanova, Leily
    Bagrov, Dmitry
    Artykov, Artem
    Gasparian, Marine
    Sizova, Svetlana
    Oleinikov, Vladimir
    Gileva, Anastasia
    Kirpichnikov, Mikhail
    Dolgikh, Dmitry
    Markvicheva, Elena
    [J]. PHARMACEUTICS, 2021, 13 (09)
  • [80] Human Lung Fibroblasts Exhibit Induced Inflammation Memory via Increased IL6 Gene Expression and Release
    Yap, Jennifer Maries Go
    Ueda, Takashi
    Kanemitsu, Yoshihiro
    Takeda, Norihisa
    Fukumitsu, Kensuke
    Fukuda, Satoshi
    Uemura, Takehiro
    Tajiri, Tomoko
    Ohkubo, Hirotsugu
    Maeno, Ken
    Ito, Yutaka
    Oguri, Testsuya
    Ugawa, Shinya
    Niimi, Akio
    [J]. FRONTIERS IN IMMUNOLOGY, 2022, 13