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<mods:namePart>Tapia, Lucía</mods:namePart>
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<mods:namePart>Bedia, Carmen</mods:namePart>
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<mods:namePart>Solà, Jordi</mods:namePart>
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<mods:namePart>Quesada Pato, Roberto</mods:namePart>
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<mods:namePart>Alfonso, Ignacio</mods:namePart>
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<mods:identifier type="doi">10.1016/j.xcrp.2024.102152</mods:identifier>
<mods:abstract>The acidic microenvironment of solid tumors is a potential source of selectivity in the anti-cancer activity of ionophores, which requires delicate control of their biophysical properties. In this context, we have systematically studied fluorine substitutions in the aromatic side chains of HCl-binding pseudopeptidic cages. Interconnected factors like chloride binding, protonation, lipophilicity, and conformation and diffusiveness of the cages can impact their ability to transport HCl through the aqueous-lipid interphase, as demonstrated by robust experimental (X-ray, nuclear magnetic resonance [NMR], fluorescence) and theoretical results. The fine-tuning of these properties allows the modulation of their pH-dependent cytotoxicity against cancer cells, from essentially non-cytotoxic at pH 7.5 (like the extracellular surroundings of healthy tissues) to highly toxic in slightly acidic microenvironments (like those around solid tumors). Thus, a distal fluorine substitution produces a big impact on the physicochemical and biological properties of the cages, improving their selectivity as potential therapeutic ionophores.</mods:abstract>
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<mods:topic>Supramolecular chemistry</mods:topic>
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<mods:topic>Cages</mods:topic>
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<mods:subject>
<mods:topic>Anion binding</mods:topic>
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<mods:topic>Ionophores</mods:topic>
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<mods:topic>Cancer cells</mods:topic>
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<mods:topic>pH</mods:topic>
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<mods:topic>Aqueous-lipid interphase</mods:topic>
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<mods:subject>
<mods:topic>Ion transport</mods:topic>
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<mods:topic>NMR</mods:topic>
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<mods:subject>
<mods:topic>Molecular dynamics</mods:topic>
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<mods:titleInfo>
<mods:title>Tuning pH-dependent cytotoxicity in cancer cells by peripheral fluorine substitution on pseudopeptidic cages</mods:title>
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