: The reaction of Pt-based anticancer agents with arsenic trioxide affords robust complexes known as arsenoplatins. The prototype of this family of anticancer compounds is arsenoplatin-1 (AP-1) that contains an As(OH)2 fragment linked to a Pt(II) moiety derived from cisplatin. Crystallographic and spectrometric studies of AP-1 binding to a B-DNA double helix dodecamer are presented here, in comparison with cisplatin and transplatin. Results reveal that AP-1, cisplatin and transplatin react differently with the DNA model system. Notably, in the AP-1/DNA systems, the Pt-As bond can break down with time and As-containing fragments can be released. These results have implications for the understanding of the mechanism of action of arsenoplatins.
On the mechanism of action of arsenoplatins: arsenoplatin-1 binding to a B-DNA dodecamer / Troisi, Romualdo; Tito, Gabriella; Ferraro, Giarita; Sica, Filomena; Massai, Lara; Geri, Andrea; Cirri, Damiano; Messori, Luigi; Merlino, Antonello. - In: DALTON TRANSACTIONS. - ISSN 1477-9226. - 53:8(2024), pp. 3476-3483. [10.1039/d3dt04302a]
On the mechanism of action of arsenoplatins: arsenoplatin-1 binding to a B-DNA dodecamer
Troisi, RomualdoPrimo
;Tito, Gabriella;Ferraro, Giarita;Sica, Filomena;Merlino, Antonello
Ultimo
2024
Abstract
: The reaction of Pt-based anticancer agents with arsenic trioxide affords robust complexes known as arsenoplatins. The prototype of this family of anticancer compounds is arsenoplatin-1 (AP-1) that contains an As(OH)2 fragment linked to a Pt(II) moiety derived from cisplatin. Crystallographic and spectrometric studies of AP-1 binding to a B-DNA double helix dodecamer are presented here, in comparison with cisplatin and transplatin. Results reveal that AP-1, cisplatin and transplatin react differently with the DNA model system. Notably, in the AP-1/DNA systems, the Pt-As bond can break down with time and As-containing fragments can be released. These results have implications for the understanding of the mechanism of action of arsenoplatins.File | Dimensione | Formato | |
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