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Exploring the Antitumor Efficacy of N-Heterocyclic Nitrilotriacetate Oxidovanadium(IV) Salts on Prostate and Breast Cancer Cells. | LitMetric

AI Article Synopsis

  • The crystal structures of two new oxidovanadium(IV) salts were identified, along with their cytotoxic effects on prostate and breast cancer cells.
  • Four N-heterocyclic salts showed strong cytotoxic action on both cancerous and normal cells.
  • The compounds' effectiveness varied based on the structure of the counterion, with one specific compound demonstrating the highest activity, while another exhibited the lowest toxicity and distinct effects on cell cycle distribution in cancer cells.

Article Abstract

The crystal structures of two newly synthesized nitrilotriacetate oxidovanadium(IV) salts, namely [QH][VO(nta)(HO)](HO) () and [(acr)H][VO(nta)(HO)](HO) (), were determined. Additionally, the cytotoxic effects of four N-heterocyclic nitrilotriacetate oxidovanadium(IV) salts-1,10-phenanthrolinium, [(phen)H][VO(nta)(HO)](HO) (), 2,2'-bipyridinium [(bpy)H][VO(nta)(HO)](HO) (), and two newly synthesized compounds () and ()-were evaluated against prostate cancer (PC3) and breast cancer (MCF-7) cells. All the compounds exhibited strong cytotoxic effects on cancer cells and normal cells (HaCaT human keratinocytes). The structure-activity relationship analysis revealed that the number and arrangement of conjugated aromatic rings in the counterion had an impact on the antitumor effect. The compound (III), the 1,10-phenanthrolinium analogue, exhibited the greatest activity, whereas the acridinium salt (II), with a different arrangement of three conjugated aromatic rings, showed the lowest toxicity. The increased concentrations of the compounds resulted in alterations to the cell cycle distribution with different effects in MCF-7 and PC3 cells. In MCF-7 cells, compounds and were observed to block the G/M phase, while compounds and were found to arrest the cell cycle in the G/G phase. In PC3 cells, all compounds increased the rates of cells in the G/G phase.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11206760PMC
http://dx.doi.org/10.3390/molecules29122924DOI Listing

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