Disruption of the intestinal clock drives dysbiosis and impaired barrier function in colorectal cancer

Menée à l'aide d'organoïdes et d'un modèle murin de cancer colorectal, cette étude démontre que la perturbation de l'horloge circadienne des cellules colorectales contribue à la progression tumorale en modifiant la composition du microbiote et la perméabilité intestinale

Résumé en anglais

Diet is a robust entrainment cue that regulates diurnal rhythms of the gut microbiome. We and others have shown that disruption of the circadian clock drives the progression of colorectal cancer (CRC). While certain bacterial species have been suggested to play driver roles in CRC, it is unknown whether the intestinal clock impinges on the microbiome to accelerate CRC pathogenesis. To address this, genetic disruption of the circadian clock, in an Apc-driven mouse model of CRC, was used to define the impact on the gut microbiome. When clock disruption is combined with CRC, metagenomic sequencing identified dysregulation of many bacterial genera including Bacteroides, Helicobacter, and Megasphaera. We identify functional changes to microbial pathways including dysregulated nucleic acid, amino acid, and carbohydrate metabolism, as well as disruption of intestinal barrier function. Our findings suggest that clock disruption impinges on microbiota composition and intestinal permeability that may contribute to CRC pathogenesis. Clock disruption and colorectal cancer drive intestinal dysbiosis.