Cytotoxicity and DNA interactions of some platinum(II) complexes with substituted benzimidazole ligands

J Enzyme Inhib Med Chem. 2012 Jun;27(3):413-8. doi: 10.3109/14756366.2011.594046. Epub 2012 Feb 3.

Abstract

In the present study, four Pt(II) complexes with 2-ethyl (1)/or benzyl (2)/or p-chlorobenzyl (3)/or 2-phenoxymethyl (4) benzimidazole carrier ligands were evaluated for their in vitro cytotoxic activities against the human HeLa cervix, oestrogen receptor-positive MCF-7 breast, and oestrogen receptor-negative MDA-MB 231 breast cancer cell lines. The plasmid DNA interactions and inhibition of the BamHI restriction enzyme activities of the complexes were also studied. Complex 3 was found to be more active than carboplatin for all examined cell lines and comparable with cisplatin, except for the HeLa cell line.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Benzimidazoles / chemistry*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • DNA / drug effects*
  • Deoxyribonuclease BamHI / antagonists & inhibitors
  • Deoxyribonuclease BamHI / metabolism
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • HeLa Cells
  • Humans
  • Ligands
  • Organoplatinum Compounds / chemical synthesis
  • Organoplatinum Compounds / chemistry
  • Organoplatinum Compounds / toxicity*
  • Plasmids
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Benzimidazoles
  • Ligands
  • Organoplatinum Compounds
  • DNA
  • benzimidazole
  • Deoxyribonuclease BamHI