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Endogenous murine microbiota member Faecalibaculum rodentium and its human homolog protect from intestinal tumor growth

The microbiota has been shown to promote intestinal tumorigenesis, but a possible anti-tumorigenic effect has also been postulated. Here, we demonstrate that changes in microbiota and mucus composition are concomitant with tumorigenesis. We identified two anti-tumorigenic strains of the microbiota,...

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Detalles Bibliográficos
Autores principales: Zagato, Elena, Pozzi, Chiara, Bertocchi, Alice, Schioppa, Tiziana, Saccheri, Fabiana, Guglietta, Silvia, Fosso, Bruno, Melocchi, Laura, Nizzoli, Giulia, Troisi, Jacopo, Marzano, Marinella, Oresta, Bianca, Spadoni, Ilaria, Atarashi, Koji, Carloni, Sara, Arioli, Stefania, Fornasa, Giulia, Asnicar, Francesco, Segata, Nicola, Guglielmetti, Simone, Honda, Kenya, Pesole, Graziano, Vermi, William, Penna, Giuseppe, Rescigno, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048616/
https://www.ncbi.nlm.nih.gov/pubmed/31988379
http://dx.doi.org/10.1038/s41564-019-0649-5
Descripción
Sumario:The microbiota has been shown to promote intestinal tumorigenesis, but a possible anti-tumorigenic effect has also been postulated. Here, we demonstrate that changes in microbiota and mucus composition are concomitant with tumorigenesis. We identified two anti-tumorigenic strains of the microbiota, Faecalibaculum rodentium and its human homolog Holdemanella biformis, which are strongly underrepresented during tumorigenesis. Reconstitution of Apc(Min/+) or AOM/DSS-treated mice with an isolate of F. rodentium (F. PB1) or its metabolic products reduced tumor growth. F. PB1 and H. biformis produced short-chain fatty acids (SCFAs) that contributed to control protein acetylation and tumor cell proliferation by inhibiting calcineurin/NFATc3 activation both in mouse and human settings. Thus, we have identified endogenous anti-tumorigenic bacterial strains with strong diagnostic, therapeutic and translational potential.