Depicting the DNA Binding and Cytotoxicity Studies against Human Colorectal Cancer of Aquabis (1-Formyl-2-Naphtholato-k2O,O′) Copper(II): A Biophysical and Molecular Docking Perspective

被引:6
|
作者
Alolayqi, Ebtisam [1 ]
Afzal, Mohd [1 ]
Alarifi, Abdullah [1 ]
Beagan, Abeer [1 ]
Muddassir, Mohd [1 ]
机构
[1] King Saud Univ, Coll Sci, Dept Chem, Riyadh 11451, Saudi Arabia
关键词
copper(II) complex; single crystal; topological analysis; MTT assay; mitochondrial pathway; SCHIFF-BASE; CRYSTAL-STRUCTURE; INTERMOLECULAR INTERACTIONS; METAL-COMPLEXES; ANTIBACTERIAL; 2-HYDROXY-1-NAPHTHALDEHYDE; MECHANISM; INTERCALATION; TRANSPORTER; VANILLIN;
D O I
10.3390/cryst12010015
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
In this study, we attempted to examine the biological activity of the copper(II)-based small molecule aquabis (1-formyl-2-naphtholato-k(2)O,O ')copper(II) (1) against colon cancer. The characterization of complex 1 was established by analytical and spectral methods in accordance with the single-crystal X-ray results. A monomeric unit of complex 1 exists in an O-4 (H2O) coordination environment with slightly distorted square pyramidal geometry (tau = ~0.1). The interaction of complex 1 with calf thymus DNA (ctDNA) was determined by employing various biophysical techniques, which revealed that complex 1 binds to ctDNA at the minor groove with a binding constant of 2.38 x 10(5) M-1. The cytotoxicity of complex 1 towards human colorectal cell line (HCT116) was evaluated by the MTT assay, which showed an IC50 value of 11.6 mu M after treatment with complex 1 for 24 h. Furthermore, the apoptotic effect induced by complex 1 was validated by DNA fragmentation pattern, which clarified that apoptosis might be regulated through the mitochondrial-mediated production of reactive oxygen species (ROS) causing DNA damage pathway. Additionally, molecular docking was also carried out to confirm the recognition of complex 1 at the minor groove.
引用
收藏
页数:16
相关论文
共 5 条
  • [1] Synthesis and characterization of Cu(II)-based anticancer chemotherapeutic agent targeting topoisomerase Iα: In vitro DNA binding, pBR322 cleavage, molecular docking studies and cytotoxicity against human cancer cell lines
    Tabassum, Sartaj
    Zaki, Mehvash
    Afzal, Mohd.
    Arjmand, Farukh
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 74 : 509 - 523
  • [2] Synthesis and crystal structure of a new copper(II) complex with N,N′-(4,4′-bithiazole-2,2′-diyl)diacetimidamide as ligand: Molecular docking, DNA-binding and cytotoxicity activity studies
    Wang, Ling-Dong
    Zheng, Kang
    Li, Yan-Tuan
    Wu, Zhi-Yong
    Yan, Cui-Wei
    JOURNAL OF MOLECULAR STRUCTURE, 2013, 1037 : 15 - 22
  • [3] Two Cu(II) complexes containing 2,4-diamino-6-(2-pyridy1)-1,3,5-triazine and amino acids: Synthesis, crystal structures, DNA/HSA binding, molecular docking, and in vitro cytotoxicity studies
    Shen, Fang
    Ou, Zhi-Bin
    Liu, Yu-Jia
    Liu, Wei
    Wang, Bing-Feng
    Mao, Zong-Wan
    Le, Xue-Yi
    INORGANICA CHIMICA ACTA, 2017, 465 : 1 - 13
  • [4] A copper(II) complex of 6-(pyrazin-2-yl)-1,3,5-triazine-2,4-diamine and L-serinate: synthesis, crystal structure, DNA-binding and molecular docking studies
    Zhang, Chun-Lian
    Zhang, Xue-Mei
    Liu, Wei
    Chen, Shi
    Le, Xue-Yi
    TRANSITION METAL CHEMISTRY, 2018, 43 (03) : 201 - 209
  • [5] DNA- and BSA-binding studies and anticancer activity against human breast cancer cells (MCF-7) of the zinc(II) complex coordinated by 5,6-dipheny1-3-(2-pyridyl)-1,2,4-triazine
    Anjomshoa, Marzieh
    Fatemi, Seyed Jamilaldin
    Torkzadeh-Mahani, Masoud
    Hadadzadeh, Hassan
    SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2014, 127 : 511 - 520