A cytidine deaminase biodegrader sensitises multiple cancer types to deoxycytidine analogue-based chemotherapies

Abstract Deoxycytidine (dC) analogues are widely used to treat solid tumours and blood cancers. However, their clinical efficacy is often limited by resistance mediated by cytidine deaminase (CDA), which converts these drugs into inactive metabolites. Existing CDA inhibitors have limited efficacy and off-target effects, highlighting the need for alternative approaches. Here, we show the development of a CDA biodegrader, an intracellular anti-CDA VHH fused to the SPOP E3 ubiquitin ligase, enabling specific CDA degradation. It effectively depletes CDA in pancreatic, lung, and acute myeloid leukaemia cancer cell lines, increasing sensitivity to dC analogues in vitro. Combined with gemcitabine, the CDA biodegrader inhibits pancreatic and lung tumour growth in vivo. Importantly, mRNA encoding the biodegrader delivered using virus-like particles achieves efficient sensitisation to gemcitabine in vitro and in vivo. This proof-of-concept study establishes targeted CDA degradation as a feasible strategy to enhance the therapeutic efficacy of dC analogues.

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Publication Details

Journal
Nature Communications
Published
2026-10-07
DOI
https://doi.org/10.1038/s41467-026-78315-0
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00
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article

A cytidine deaminase biodegrader sensitises multiple cancer types to deoxycytidine analogue-based chemotherapies

Étienne Chatelut, Fabienne Thomas, Nicolas Béry, Charlene Lopez et al.
Nature Communications
Protein Degradation and Inhibitors
article

A cytidine deaminase biodegrader sensitises multiple cancer types to deoxycytidine analogue-based chemotherapies

Étienne Chatelut, Fabienne Thomas, Nicolas Béry, Charlene Lopez, Carine Joffre, Constance Manso, Marie Sorbara, Laura Poillet-Perez, Margaux Vienne, Odile Burlet‐Schiltz, Lætitia Ligat, Pierre Cordelier, Anaïs Faihy, Margot Cristol, Manon Gervais, Alexandre Stella, Naïma Hanoun, Ben Allal
article en

Abstract

Abstract Deoxycytidine (dC) analogues are widely used to treat solid tumours and blood cancers. However, their clinical efficacy is often limited by resistance mediated by cytidine deaminase (CDA), which converts these drugs into inactive metabolites. Existing CDA inhibitors have limited efficacy and off-target effects, highlighting the need for alternative approaches. Here, we show the development of a CDA biodegrader, an intracellular anti-CDA VHH fused to the SPOP E3 ubiquitin ligase, enabling specific CDA degradation. It effectively depletes CDA in pancreatic, lung, and acute myeloid leukaemia cancer cell lines, increasing sensitivity to dC analogues in vitro. Combined with gemcitabine, the CDA biodegrader inhibits pancreatic and lung tumour growth in vivo. Importantly, mRNA encoding the biodegrader delivered using virus-like particles achieves efficient sensitisation to gemcitabine in vitro and in vivo. This proof-of-concept study establishes targeted CDA degradation as a feasible strategy to enhance the therapeutic efficacy of dC analogues.

Nature Communications
Centre National de la Recherche Scientifique (FR), Inserm (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Centre Hospitalier Universitaire de Toulouse (FR), Centre de Recherches en Cancérologie de Toulouse (FR), Institut de Pharmacologie et de Biologie Structurale (FR), Institut Claudius Regaud (FR), Université de Toulouse (FR)
Openalex Percentile: Top 22%
Protein Degradation and Inhibitors
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