Suboptimal oxygen supply in solid tumors controls a variety of cancer hallmarks and impairs responsiveness to anticancer treatments. Yet, tools to visualize hypoxia in cancer are still limited. Here we present an application of the tetrazine-dienophile inverse-electron demand Diels-Alder (IEDDA) reaction for hypoxia visualization. In this approach, trans-cyclooctene-clickable 2-nitroimidazoles work in combination with tetrazine-functionalized probes for live imaging of differential levels of hypoxia in two-dimensional (2D) and three-dimensional (3D) models. We used tetrazine-based fluorescent probes to determine oxygen levels in cell monolayers, spheroids, and patient-derived organoids, and applied a “click-to-release” approach to evaluate the diffusion of the released probe in the surrounding peripheral regions, allowing to quantify the bystander effect. Given the compatibility of the tetrazine-dienophile click reaction with living organisms, the combination of clickable 2-nitroimidazoles with tetrazine-based reporters opens a new avenue for in vivo hypoxia imaging.

Tetrazine-based bioorthogonal reactions to image hypoxia in cancer cells

Boumya, Sara;Boero, Chiara
Membro del Collaboration Group
;
De Luigi, Edoardo;Foglietta, Federica;Ferreira-Alves, Gustavo;Mancardi, Daniele;Spyrakis, Francesca;Lazzarato, Loretta;Serafini, Marta
2026-01-01

Abstract

Suboptimal oxygen supply in solid tumors controls a variety of cancer hallmarks and impairs responsiveness to anticancer treatments. Yet, tools to visualize hypoxia in cancer are still limited. Here we present an application of the tetrazine-dienophile inverse-electron demand Diels-Alder (IEDDA) reaction for hypoxia visualization. In this approach, trans-cyclooctene-clickable 2-nitroimidazoles work in combination with tetrazine-functionalized probes for live imaging of differential levels of hypoxia in two-dimensional (2D) and three-dimensional (3D) models. We used tetrazine-based fluorescent probes to determine oxygen levels in cell monolayers, spheroids, and patient-derived organoids, and applied a “click-to-release” approach to evaluate the diffusion of the released probe in the surrounding peripheral regions, allowing to quantify the bystander effect. Given the compatibility of the tetrazine-dienophile click reaction with living organisms, the combination of clickable 2-nitroimidazoles with tetrazine-based reporters opens a new avenue for in vivo hypoxia imaging.
2026
29
9
117290
117296
3D cellular models; bystander effect; Cell biology; Chemistry; click chemistry; fluorescence; hypoxia; Imaging methods in chemistry; Microenvironment; tetrazine bioorthogonal reactions
Boumya, Sara; Boero, Chiara; De Luigi, Edoardo; Foglietta, Federica; Ferreira-Alves, Gustavo; Mancardi, Daniele; Lupo, Barbara; Spyrakis, Francesca; L...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/2164630
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