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Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2)

Polyoxometalates (POMs) exhibit unique structural characteristics and excellent physical and chemical properties, which have attracted significant attention from scholars in the fields of anticancer research and chemotherapy. Herein, we successfully synthesized and structurally characterized two nov...

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Autores principales: Shi, Fumei, Chen, Yilan, Dong, Chuanheng, Wang, Jiajia, Song, Chunman, Zhang, Yalin, Li, Zhen, Huang, Xianqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574323/
https://www.ncbi.nlm.nih.gov/pubmed/37836686
http://dx.doi.org/10.3390/molecules28196843
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author Shi, Fumei
Chen, Yilan
Dong, Chuanheng
Wang, Jiajia
Song, Chunman
Zhang, Yalin
Li, Zhen
Huang, Xianqiang
author_facet Shi, Fumei
Chen, Yilan
Dong, Chuanheng
Wang, Jiajia
Song, Chunman
Zhang, Yalin
Li, Zhen
Huang, Xianqiang
author_sort Shi, Fumei
collection PubMed
description Polyoxometalates (POMs) exhibit unique structural characteristics and excellent physical and chemical properties, which have attracted significant attention from scholars in the fields of anticancer research and chemotherapy. Herein, we successfully synthesized and structurally characterized two novel polyoxovanadates (POVs), denoted as POVs-1 and POVs-2, where [M(1-vIM)(4)](2)[V(V)(4)O(12)]·H(2)O (M: Ni(II) and Mn(II), 1-vinylimidazole abbreviated as 1-vIM) serve as ligands. The two POVs are isomeric and consist of fundamental structural units, each comprising one [V(4)O(12)](4−) cluster, two [M(1-vIM)(4)](2+) cations, and one water molecule. Subsequently, we evaluated the cell viability of human hepatocellular carcinoma (HepG-2) cells treated with the synthesized POVs using the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazoliumbromide) assay. And the changes in cell nucleus morphology, mitochondrial membrane potential (Δψ(m)), and reactive oxygen species levels in HepG-2 exposed to POVs were monitored using specific fluorescent staining techniques. Both hybrid POVs showed potent inhibitory activities, induing apoptosis in HepG-2 cells along with significant mitochondria dysfunction and a burst of reactive oxygen species. Notably, the inhibitory effects of POVs-2 were more pronounced than those of POVs-1, which is primarily attributed to the different transition metal ions present. These findings underscore the intricate relationship between the metal components, structural characteristics, and the observed antitumor activities in HepG-2 cells.
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spelling pubmed-105743232023-10-14 Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2) Shi, Fumei Chen, Yilan Dong, Chuanheng Wang, Jiajia Song, Chunman Zhang, Yalin Li, Zhen Huang, Xianqiang Molecules Article Polyoxometalates (POMs) exhibit unique structural characteristics and excellent physical and chemical properties, which have attracted significant attention from scholars in the fields of anticancer research and chemotherapy. Herein, we successfully synthesized and structurally characterized two novel polyoxovanadates (POVs), denoted as POVs-1 and POVs-2, where [M(1-vIM)(4)](2)[V(V)(4)O(12)]·H(2)O (M: Ni(II) and Mn(II), 1-vinylimidazole abbreviated as 1-vIM) serve as ligands. The two POVs are isomeric and consist of fundamental structural units, each comprising one [V(4)O(12)](4−) cluster, two [M(1-vIM)(4)](2+) cations, and one water molecule. Subsequently, we evaluated the cell viability of human hepatocellular carcinoma (HepG-2) cells treated with the synthesized POVs using the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazoliumbromide) assay. And the changes in cell nucleus morphology, mitochondrial membrane potential (Δψ(m)), and reactive oxygen species levels in HepG-2 exposed to POVs were monitored using specific fluorescent staining techniques. Both hybrid POVs showed potent inhibitory activities, induing apoptosis in HepG-2 cells along with significant mitochondria dysfunction and a burst of reactive oxygen species. Notably, the inhibitory effects of POVs-2 were more pronounced than those of POVs-1, which is primarily attributed to the different transition metal ions present. These findings underscore the intricate relationship between the metal components, structural characteristics, and the observed antitumor activities in HepG-2 cells. MDPI 2023-09-28 /pmc/articles/PMC10574323/ /pubmed/37836686 http://dx.doi.org/10.3390/molecules28196843 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shi, Fumei
Chen, Yilan
Dong, Chuanheng
Wang, Jiajia
Song, Chunman
Zhang, Yalin
Li, Zhen
Huang, Xianqiang
Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2)
title Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2)
title_full Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2)
title_fullStr Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2)
title_full_unstemmed Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2)
title_short Ni/Mn-Complex-Tethered Tetranuclear Polyoxovanadates: Crystal Structure and Inhibitory Activity on Human Hepatocellular Carcinoma (HepG-2)
title_sort ni/mn-complex-tethered tetranuclear polyoxovanadates: crystal structure and inhibitory activity on human hepatocellular carcinoma (hepg-2)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574323/
https://www.ncbi.nlm.nih.gov/pubmed/37836686
http://dx.doi.org/10.3390/molecules28196843
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