DNA intercalators based on (1,10-phenanthrolin-2-yl)isoxazolidin-5-yl core with better growth inhibition and selectivity than cisplatin upon head and neck squamous cells carcinoma

May 22, 2018

Title

DNA intercalators based on (1,10-phenanthrolin-2-yl)isoxazolidin-5-yl core with better growth inhibition and selectivity than cisplatin upon head and neck squamous cells carcinoma

Author

Maria G. Varrica, Chiara Zagni, Placido G. Mineo, Giuseppe Floresta, Giulia Monciino, Venerando Pistarà, Antonio Abbadessa, Angelo Nicosia, Rogerio M. Castilho, Emanuele Amata, Antonio Rescifina

Year

2018

Journal

European Journal of Medicinal Chemistry

Abstract

((3RS,5SR)- and ((3RS,5RS)-2-(2-methoxybenzyl)-3-(1,10-phenanthrolin-2-yl)isoxazolidin-5-yl)methanol have been synthesized, according to 1,3-dipolar cycloaddition methodology, as DNA intercalating agents and evaluated for their anticancer activity against human cervical carcinoma HeLa and head and neck squamous cells carcinoma cell lines. The synthesized compounds exhibited good cytotoxic activity with IC50 better than cisplatin, used as the main and effective treatment for HNSCC, and a 24.3–72.0-fold selectivity respect to the 184B5 non-cancerous immortalized breast epithelial cell lines. Unwinding assay, circular dichroism data, and Uv-vis melting experiments confirmed that these compounds act as DNA intercalators with a binding constant in the order of 104 M−1. Docking studies showed that both compounds can interact as intercalating agent with both poly-d(AT)2and poly-d(GC)2, preferring an entrance by the minor groove of the poly-d(AT)2.

Instrument

J-815

Keywords

Circular dichroism, DNA structure, Ligand binding, Biochemistry, Medicinal