Evaluation of Anticancer Activity of Nucleoside–Nitric Oxide Photo-Donor Hybrids

Author:

Marchesi Elena1ORCID,Melloni Elisabetta23ORCID,Casciano Fabio23ORCID,Pozza Elena2ORCID,Argazzi Roberto14,De Risi Carmela1ORCID,Preti Lorenzo5ORCID,Perrone Daniela5ORCID,Navacchia Maria Luisa4ORCID

Affiliation:

1. Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara, 44121 Ferrara, Italy

2. Department of Translational Medicine, University of Ferrara, 44121 Ferrara, Italy

3. LTTA Centre, University of Ferrara, 44121 Ferrara, Italy

4. Institute for Organic Synthesis and Photoreactivity (ISOF), National Research Council of Italy (CNR), 40129 Bologna, Italy

5. Department of Environmental and Prevention Sciences, University of Ferrara, 44121 Ferrara, Italy

Abstract

Herein, we report the synthesis of a new hybrid compound based on a 2′-deoxyuridine nucleoside conjugated with a NO photo-donor moiety (dU-t-NO) via CuAAC click chemistry. Hybrid dU-t-NO, as well as two previously reported 2′-deoxyadenosine based hybrids (dAdo-S-NO and dAdo-t-NO), were evaluated for their cytotoxic and cytostatic activities in selected cancer cell lines. dAdo-S-NO and dAdo-t-NO hybrids displayed higher activity with respect to dU-t-NO. All hybrids showed effective release of NO in the micromolar range. The photochemical behavior of the newly reported hybrid, dU-t-NO, was studied in the RKO colon carcinoma cell line, whereas the dAdo-t-NO hybrid was tested in both colon carcinoma RKO and hepatocarcinoma Hep 3B2.1-7 cell lines to evaluate the potential effect of NO released upon irradiation on cell viability. A customized irradiation apparatus for in vitro experiments was also designed.

Publisher

MDPI AG

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