Karta Jessica, Meyers Marianne, Rodriguez Fabien, Koncina Eric, Gilson Cedric, Klein Eliane, Gabola Monica, Benzarti Mohaned, Pérez Escriva Pau, Molina Tijeras Jose Alberto, Correia Tavares Bernardino Catarina, Ponath Falk, Carpentier Anais, Pujabet Mònica Aguilera, Schmoetten Maryse, Tsenkova Mina, Saoud Perla, Gaigneaux Anthoula, Ternes Dominik, Alonso Lidia, Zügel Nikolaus, Willemssen Eric, Koppes Philippe, Léonard Daniel, Casanova Luis Perez, Haan Serge, Mittelbronn Michel, Meiser Johannes, Pozdeev Vitaly I, Vogel Jörg, Nuciforo Paolo G, Wilmes Paul, Letellier Elisabeth
Department of Life Sciences and Medicine (DLSM), Faculty of Science, Technology and Medicine, University of Luxembourg, Esch-sur-Alzette, Luxembourg.
Institute of Molecular Infection Biology, University of Würzburg, Würzburg, Germany.
EMBO J. 2025 Aug 22. doi: 10.1038/s44318-025-00542-w.
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.
肠道微生物物种通过与肿瘤或免疫细胞相互作用促进结直肠癌(CRC)的发生,然而,与CRC相关的细菌是否与肿瘤微环境的基质成分相互作用仍不清楚。在此,我们报告了与CRC相关的具核梭杆菌与癌症相关成纤维细胞(CAF)之间的相互作用,并表明具核梭杆菌存在于体内小鼠CRC模型的基质区室中,且能够附着并侵入CAF。暴露于具核梭杆菌的CAF表现出明显的炎性CAF(iCAF)表型,其特征为既定的iCAF标志物表达升高、分泌促炎细胞因子(如CXCL1、IL-6和IL-8)、产生活性氧(ROS)以及代谢活性增加。在共培养实验中,癌细胞与经具核梭杆菌刺激的CAF之间的相互作用增强了侵袭能力,这一发现也在体内得到了进一步验证。总之,我们的研究结果表明肿瘤微生物群通过影响癌症相关成纤维细胞重塑肿瘤微环境,在CRC进展中发挥作用,这为靶向CRC提出了新的治疗策略。