Pósa, Vivien and Stefanelli, Alessia and Bormio Nunes, Julia H. and Hager, Sonja and Mathuber, Marlene and May, Nóra Veronika and Enyedy, Éva Anna (2022) Thiosemicarbazone Derivatives Developed to Overcome COTI-2 Resistance. CANCERS, 14 (18). No. 4455. ISSN 2072-6694
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Abstract
COTI-2 is currently being evaluated in a phase I clinical trial for the treatment of gynecological and other solid cancers. As a thiosemicarbazone, this compound contains an N,N,S-chelating moiety and is, therefore, expected to bind endogenous metal ions. However, besides zinc, the metal interaction properties of COTI-2 have not been investigated in detail so far. This is unexpected, as we have recently shown that COTI-2 forms stable ternary complexes with copper and glutathione, which renders this drug a substrate for the resistance efflux transporter ABCC1. Herein, the complex formation of COTI-2, two novel terminal N-disubstituted derivatives (COTI-NMe2 and COTI-NMeCy), and the non-substituted analogue (COTI-NH2) with iron, copper, and zinc ions was characterized in detail. Furthermore, their activities against drug-resistant cancer cells was investigated in comparison to COTI-2 and Triapine. These data revealed that, besides zinc, also iron and copper ions need to be considered to play a role in the mode of action and resistance development of these thiosemicarbazones. Moreover, we identified COTI-NMe2 as an interesting new drug candidate with improved anticancer activity and resistance profile.
Item Type: | Article |
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Uncontrolled Keywords: | thiosemicarbazones; COTI-2; zinc; copper; iron; metal binding; stability constants; resistance; anticancer; p53 |
Subjects: | Q Science / természettudomány > QD Chemistry / kémia |
SWORD Depositor: | MTMT SWORD |
Depositing User: | MTMT SWORD |
Date Deposited: | 19 Sep 2022 07:46 |
Last Modified: | 19 Sep 2022 07:46 |
URI: | http://real.mtak.hu/id/eprint/148890 |
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