The EMBO Journal · 2025 · 13 citations · 68 references
MedicineMicrobiologyOncologyInflammationMetastasisTumor MicroenvironmentCancer-associated FibroblastsColorectal CancerInflammation-associated CarcinogenesisInflammatory SignalingTumor Microenvironment InteractionsTumor-stroma InteractionsCancer-associated Fibroblast InteractionsCo-culture ModelsFusobacterium SpeciesHost-microbiome Interactions In CancerPro-inflammatory ChemokinesReactive Oxygen Species GenerationStromal ArchitectureTumor Microenvironment Effects
Gut microbial species contribute to colorectal cancer (CRC) by interacting with tumor or immune cells, however if CRC-associated bacteria engage with stromal components of the tumor microenvironment remains unclear. Here, we report interaction between the CRC-associated bacterium Fusobacterium nucleatum and cancer-associated fibroblasts (CAFs), and show that F. nucleatum is present in the stromal compartment in murine CRC models in vivo and can attach to and invade CAFs. F. nucleatum-exposed CAFs exhibit a pronounced inflammatory-CAF (iCAF) phenotype, marked by elevated expression of established iCAF markers, secretion of pro-inflammatory cytokines such as CXCL1, IL-6 and IL-8, generation of reactive oxygen species (ROS), and an increased metabolic activity. In co-culture experiments, the interaction of cancer cells with F. nucleatum-stimulated CAFs enhances invasion, a finding further validated in vivo. Altogether, our results point to a role for the tumor microbiome in CRC progression by remodeling the tumor microenvironment through its influence on cancer-associated fibroblasts, suggesting novel therapeutic strategies for targeting CRC.
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Medicine, Cancer Biology, Pathology +17
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