par Casini, Angela;Messori, Luigi;Orioli, Pierluigi;Gielen, Marcel 
;Kemmer, Martine;Willem, Rudolph
Référence Journal of inorganic biochemistry, 85, 4, page (297-300)
Publication Publié, 2001
;Kemmer, Martine;Willem, Rudolph Référence Journal of inorganic biochemistry, 85, 4, page (297-300)
Publication Publié, 2001
Article révisé par les pairs
| Résumé : | The reactions with DNA of two antitumor active organotin(IV) compounds, the dimer of bis[(di-n-butyl 3,6-dioxaheptanoato)tin] (C52H108Sn4O1·2H2O), compound 1, and tri-n-butyltin 3,6,9-trioxodecanoate (C19H40SnO5·1/2H2O), 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. Copyright © 2001 Elsevier Science B.V. |
