Interactions of two cytotoxic organotin(IV) compounds with calf thymus DNA

  • A Casini
  • , L Messori*
  • , P Orioli
  • , M Gielen
  • , M Kemmer
  • , R Willem
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

59 Citations (Scopus)

Abstract

The reactions with DNA of two antitumor active organotin(IV) compounds, the dimer of bis[(di-n-butyl 3,6-dioxaheptanoato)tin] (C52H108Sn4O1. 2H(2)O), compound 1, and tri-n-butyltin 3,6,9-trioxodecanoate (C19H4OSnO5.1/2H(2)O), compound 2, were analysed by circular dichroism, DNA melting experiments and gel mobility shift assays. It is found that both complexes modify only slightly the B-type circular dichroism spectroscopy (CD) spectrum of calf thymus DNA. On the other hand, both complexes were found to affect significantly the parameters of the thermally induced helix-to-coil transition. Addition of 1 or 2 to calf thymus DNA samples does not favor DNA renaturation after melting ruling out formation of interstrand crosslinks. Moreover, the effects of both compounds on plasmid DNA gel mobility were investigated. From the analysis of the present results it is inferred that both organotin(IV) compounds do interact with DNA, probably at the level of the phosphate groups. (C) 2001 Elsevier Science BV All rights reserved.

Original languageEnglish
Pages (from-to)297-300
Number of pages4
JournalJournal of Inorganic Biochemistry
Volume85
Issue number4
DOIs
Publication statusPublished - Jul-2001
Externally publishedYes

Keywords

  • organotin compounds
  • DNA
  • circular dichroism
  • DNA melting
  • gel electrophoresis
  • COMPLEXES
  • COORDINATION
  • LIGANDS
  • ACID

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