Docking and in vitro molecular biology studies of p-anisidine-appended 1-hydroxy-2-acetonapthanone Schiff base lanthanum(iii) complexes. Issue 28 (24th April 2020)

• Record Type: Journal Article
• Authors: Sathiyanarayanan, V.; Prasath, P. Varun; Sekhar, P. Chandra; Ravichandran, K.; Easwaramoorthy, D.; Mohammad, Faruq; Al-Lohedan, Hamad A.; Oh, Won Chun; Sagadevan, Suresh
• Is Part Of: RSC advances. Volume 10:Issue 28(2020)
• Page Start: 16457
• Page End: 16472
• Publication Date: 2020-04-24
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0ra01936d
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : A new series of lanthanum(iii ) complexes was synthesized using a p -anisidine-appended 1-hydroxy-2-acetonapthanone (3 ) Schiff base and characterized via spectroscopic methods. Abstract : A new series of lanthanum(iii ) complexes was synthesized using a p -anisidine-appended 1-hydroxy-2-acetonapthanone (3 ) Schiff base and characterized via spectroscopic methods. The ligand was synthesized via sonication and the crystalline product was characterized using X-ray crystallography. The genotoxicity of the compound was assessed primarily by the bacterial reverse mutation (Ames) test and the in vitro mammalian chromosome aberration test; in both cases, the samarium complex 5 was found to be non-mutagenic. The anti-tumor activity of complexes 4, 5, and 6 was assayed against HeLa tumor cells and screened using the MTT assay. The IC50 value of complex 5 was found to be 34 ± 1.2 μg mL −1 and this compound exhibited superior activity towards the cells compared to 4 and 6 . These results were further confirmed by Hoechst 33258 staining and AO/EI dual staining, which indicated that the cells underwent an apoptosis mechanism in a dose-dependent manner. The apoptosis was further confirmed by the formation of ladders in the DNA fragmentation assay, and the western blot analysis of complex 5 suggested that the cells underwent the caspase-3-dependent pathway with PARP cleavage. Furthermore, the docking studies of complex 5 with HSA showed that it was situated in a hydrophilic cavity held by the electrostatic attraction of four hydrogen-bonding interactions. PDB ID:; 1BNA binds with complex 5 via strong π–π stacking interactions, which facilitate binding with the major grooves of DNA strands. The above-mentioned results illustrate that for complex 5, mitochondrion-mediated apoptosis occurs via caspase-3 activation. Complex 5 binds with DNA via intercalation because of S-phase cell cycle arrest in the HeLa cells.