In vitro cytotoxic potential and mechanism of action of selected coumarins, using human renal cell lines

Gregory J. Finn, Emma Kenealy, Bernadette S. Creaven, Denise A. Egan

Research output: Contribution to journalArticlepeer-review

Abstract

This study determined the selective cytotoxicity of eight coumarin compounds to human renal carcinoma cells, relative to non-carcinoma proximal tubular cells. Selectivity cytotoxicity was observed following exposure to 6-nitro-7-hydroxycoumarin (6-NO2-7-OHC) and 7,8-dihydroxycoumarin (7,8-OHC). 6-NO2-7-OHC induced cytotoxicity was irreversible in both cell lines, unlike 7,8-OHC, which was reversible in the carcinoma cells only. Mobility shift and BrdU incorporation assays showed that both compounds did not intercalate DNA but had a concentration-dependent inhibitory effect on its synthesis. All coumarins studied were found to be non-mutagenic using the standard Ames test. These results would suggest that 6-NO2-7-OHC and 7,8-OHC might have a therapeutic role to play in the treatment of renal cell carcinoma.

Original languageEnglish
Pages (from-to)61-68
Number of pages8
JournalCancer Letters
Volume183
Issue number1
DOIs
Publication statusPublished - 8 Sep 2002
Externally publishedYes

Keywords

  • Daphnetin
  • Esculetin
  • Nitrocoumarins
  • Renal cell carcinoma

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