Biological evaluation of redox stable cisplatin/Cu(II)-DNA adducts as potential anticancer agents. Issue 2 (17th January 2016)

• Record Type: Journal Article
• Authors: Kathiresan, Sellamuthu; Dhivya, Raman; Vigneshwar, Murugesan; Rajasekaran, Marichamy; Ranjani, Jyothi; Rajendhran, Jeyaprakash; Srinivasan, Sankaran; Mugesh, Subramanian; Murugan, Maruthamuthu; Athappan, Periakaruppan; Annaraj, Jamespandi
• Is Part Of: Journal of coordination chemistry. Volume 69:Issue 2(2016)
• Page Start: 238
• Page End: 252
• Publication Date: 2016-01-17
• Subjects: Copper complexes -- DNA-binding -- molecular docking -- MTT assay -- cytotoxicity; Coordination compounds -- Periodicals; 541.2242
• DOI: 10.1080/00958972.2015.1105366
• Languages: English
• ISSNs: 0095-8972

Abstract

Abstract: A series of non-enolizable β-diketonate-based copper(II) complexes with LCuCl2 [L = Knoevenagel condensates of curcumin (Salcimine) and methylacetoacetate (SalMaA)-based Schiff bases] chromospheres as functional models of chemotherapy drug cisplatin were investigated for their covalent interaction with herring sperm DNA. The synthesis and structural characterization of1a and1b have been reported in our previous article. However, their DNA interactions and cytotoxicity properties were not studied. These analyses have been carried out mainly through electrochemical techniques supplemented with spectral, relative viscosity, gel electrophoresis techniques, and AGS cancer cells using MTT assay. The cytotoxic activities of the ligand, curcumin-based copper complex, and cisplatin were tested against the AGS cancer cell line under similar experimental conditions showing that the complex exhibited cancer cell inhibitory rate closer to cisplatin even at low concentration. This was also seen in the docking of the Cu-complex onto a rich guanine B-DNA decamer, where a Cu–N3(guanine) interaction instead of Pt-N7 as cisplatin is detected. The obtained results in this study prove that these complexes could be a promising substitute for cisplatin as a new family of non-platinum-based anticancer metallo-drugs after in vivo tests on animal models. Abstract :