{"id":23139,"date":"2023-10-27T08:47:10","date_gmt":"2023-10-27T06:47:10","guid":{"rendered":"https:\/\/idibell.cat\/en\/?post_type=agenda&p=23139"},"modified":"2024-01-17T13:57:41","modified_gmt":"2024-01-17T12:57:41","slug":"idibellseminars-gut-microbiome-disturbance-and-mucosal-barrier-dysfunction-in-gastrointestinal-cancer-development","status":"publish","type":"agenda","link":"https:\/\/idibell.cat\/en\/agenda\/idibellseminars-gut-microbiome-disturbance-and-mucosal-barrier-dysfunction-in-gastrointestinal-cancer-development\/","title":{"rendered":"#IDIBELLseminars: Gut microbiome disturbance and mucosal barrier dysfunction in gastrointestinal cancer development"},"content":{"rendered":"

Microbiome disturbance (reduced diversity, increased growth\/activity of pathogenic species) and metabolic action associated with gut barrier dysfunction and inflammation may influence development of gastrointestinal cancers. In multicentre prospective and patient cohorts of colorectal, hepatobiliary, and pancreatic cancers, we have been assessing these links by measuring serum immune responses to bacterial antigens, serum biomarkers of gut barrier integrity, and microbial abundance in tumour tissues. Additionally, we have recently applied the concept of Mendelian randomization (MR) analyses to examine the association of genetically predicted microbial profiles and metabolite concentrations with risk of hepatobiliary and pancreatic cancers. Together, our results support the hypothesis that gut barrier dysfunction and microbial translocation and metabolism may influence the development of these cancers (example PMIDs: 28372583, 26823475, 31481495, 29377173, 32332031, 33874856, 37338617, 37158960).<\/p>\n

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