IDDF2024-ABS-0130 Faecalibacterium prausnitzii antagonizes helicobacter pylori colonization and inhibits gastric carcinogenesis

• Published in: Gut Vol. 73; no. Suppl 2; p. A129
• Main Authors: Jiang, Lanping, Fu, Kaili, Wong, Chi Chun, Li, Qing, Liu, Dehua, Xie, Mingxu, Li, Tianhui, Lau, Harry Cheuk-Hay, Zhang, Xiang
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group Ltd and British Society of Gastroenterology 01.08.2024; BMJ Publishing Group LTD
• Subjects: Allografts; Animal models; Apoptosis; Atrophy; Basic Gastroenterology; Carcinogenesis; Cell culture; Cell cycle; Colonization; Faecalibacterium prausnitzii; Gastritis; Helicobacter pylori; Metaplasia; Microscopy; Molecular modelling; Organoids; Phosphopyruvate hydratase; Probiotics; Scanning electron microscopy; TLR4 protein; Toll-like receptors; Transmission electron microscopy; Tumorigenesis; Wnt protein; Xenografts; β-Catenin
• ISSN: 0017-5749; 1468-3288
• DOI: 10.1136/gutjnl-2024-IDDF.70

BackgroundProbiotics could protect against cancers, however, the roles of probiotics in inhibiting GC and affecting H. pylori infection are largely unclear. We first identified Faecalibacterium prausnitzii is depleted in GC. We aimed to evaluate the antitumorigenic function and molecular mechanism of F. prausnitzii in GC and its interplay with H. pylori.Methods F. prausnitzii abundance was determined in 1343 human subjects consisting of 48 healthy controls (HC), 192 superficial gastritis (SG), 130 atrophy gastritis (AG), 123 intestinal metaplasia (IM), 80 gastric epithelial dysplasia (GED), 456 cancer adjacent normal (CAN) and 407 GC. The effect of F. prausnitzii on GC was evaluated in GC cells, patient-derived organoids (G9T, POA145), human GC xenograft, YTN16 allografts and N -methyl- N -nitrosourea (MNU) induced GC tumorigenesis mouse models. F. prausnitzii attachment to GC cells and its impact on H. pylori colonization was determined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) and was validated in mouse models.Results F. prausnitzii is significantly depleted in GC patients compared to non-GC (SG, AG, IM, GED or CAN) (P<0.001). F. prausnitzii gavage reduced the colonization of H. pylori SS1 (P=0.02) and 10996 (P<0.0001) in stomach of mice through competing for their common receptor α-enolase on GC cells. Beyond inhibiting H. pylori, F. prausnitzii conditioned medium (F. p CM) inhibited GC cell growth (P<0.0001) by inducing apoptosis (P<0.05) and G1/S cell cycle arrest (P=0.003). Consistently, F. p CM suppressed GC patient-derived organoid growth (P<0.0001). F. prausnitzii gavage inhibited growth of MKN74 xenografts (P<0.0001) and YTN16 allografts (P<0.0001) in mice. Moreover, F. prausnitzii gavage reduced tumor number (P=0.037) and tumor volume (P=0.012) in MNU-induced gastric carcinogenesis. Metabolic profiling of F. p CM revealed butyrate as the top enriched metabolite. Mechanistically, butyrate is directly bound to Toll-Like Receptor 4 (TLR4) on GC cells (Kd: 5.52µM), leading to Wnt/β-catenin signaling inhibition to suppress GC development.Conclusions F. prausnitzii is thus a promising prophylactic for GC prevention and anti-H. pylori therapy.