Targeted therapies for inflammatory bowel disease and colorectal cancer: An increasing need for microbiota-intestinal mutualism

dc.contributor.authorGiovanni, Tomasello
dc.contributor.authorPietro, Tralongo
dc.contributor.authorAbdo, Jurjus
dc.contributor.authorDaouk, Hisham
dc.contributor.authorHajj Hussein, Inaya Abdallah
dc.contributor.authorMichel, Matar
dc.contributor.authorLeone, Angelo
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:36:32Z
dc.date.available2025-01-24T11:36:32Z
dc.date.issued2015
dc.description.abstractThe involvement of intestinal microbiota and dysbiosis in the pathogenesis of inflammatory bowel disease (IBD) and colorectal cancer (CRC) is a well-established fact to be taken into real consideration when developing tartgeted therapies. This review aimed to depict what advances in our understanding of the role of intestinal flora in the pathogenesis of IBD and CRC is shaping up the therapeutic protocols of their management. It was demonstrated that there is a circadian regulation of colocytes gene expression in response to microbiota. In addition, dysbiosis leading to a decrease in microbiome biodiversity was also described in IBD patients whereby thick layers of adherent mucosa associated bacteria exist both in ulcerative colitis (UC) and Crohn's disease (CD). Probiotics based approaches using lactobacilli and Bibidobacteria improved clinical symptoms of IBD's through the GALT immune modulation. In addition, fecal microbiota transplantation (FMT) has also been used for IBD treatment. It consists of transferring gastrointestinal microbiota from a healthy donor to an IBD patient by duodenal infusion of liquid stool suspension to establish microbial homeostasis. The passage of bacteria in the injured mucosal zone triggers chronic inflammation and eventually CRC development by creating a carcinogenic environment. Actually, high level of Fusobacterium nucleatun and other bacteria are prevalent in CRC patients, thus suggesting a potential role of these organisms in the initiation and progression processes due to the production of genotoxic metabolites causing a direct damage to DNA integrity. Moreover, regular probiotics intake was shown to actively prevent the whole process. In conclusion, the mutualistic relationship between microbiota and colonic mucosa proved useful in depicting some of the dynamics of the initiation and development of IBD and CRC. Therapies oriented towards establishing equilibrium of intestinal microbiota may represent the key strategy to switch off chronic inflammatory processes hitting colonic mucosa, thus preventing the onset of CRC.
dc.identifier.doihttps://doi.org/10.11910/2227-6394.2015.03.02.11
dc.identifier.eid2-s2.0-85043632386
dc.identifier.urihttp://hdl.handle.net/10938/28624
dc.language.isoen
dc.publisherThird Party Medicine International Publishing Group Co. Limited
dc.relation.ispartofJournal of International Translational Medicine
dc.sourceScopus
dc.subjectColorectal cancer
dc.subjectInflammatory bowel disease
dc.subjectMicrobiota
dc.subjectTherapy
dc.subjectUlcerative colitis
dc.subjectAngiogenin 4
dc.subjectCaspase recruitment domain protein 15
dc.subjectChaperonin 60
dc.subjectClaudin 12
dc.subjectClaudin 2
dc.subjectColecalciferol receptor
dc.subjectEarly pregnancy factor
dc.subjectEpiregulin
dc.subjectHeat shock protein 70
dc.subjectHeat shock protein 90
dc.subjectHla b27 antigen
dc.subjectInterleukin 17
dc.subjectInterleukin 6
dc.subjectMembrane protein
dc.subjectPattern recognition receptor
dc.subjectPeroxisome proliferator activated receptor alpha
dc.subjectProbiotic agent
dc.subjectRar related orphan receptor alpha
dc.subjectSynaptotagmin i
dc.subjectThymic stromal lymphopoietin
dc.subjectToll like receptor 1
dc.subjectToll like receptor 2
dc.subjectToll like receptor 4
dc.subjectToll like receptor 5
dc.subjectToll like receptor 9
dc.subjectTranscription factor ap 1
dc.subjectTranscription factor arntl
dc.subjectTransforming growth factor beta
dc.subjectTumor necrosis factor
dc.subjectUnclassified drug
dc.subjectUnindexed drug
dc.subjectBifidobacterium
dc.subjectCircadian rhythm
dc.subjectColon cell
dc.subjectCrohn disease
dc.subjectDna damage
dc.subjectDysbiosis
dc.subjectFecal microbiota transplantation
dc.subjectGene expression
dc.subjectHuman
dc.subjectImmunomodulation
dc.subjectIntestine flora
dc.subjectIntestine lymphatic tissue
dc.subjectIntracellular signaling
dc.subjectLactobacillus
dc.subjectMetabolite
dc.subjectMicrobial diversity
dc.subjectMolecularly targeted therapy
dc.subjectNonhuman
dc.subjectProtein expression
dc.subjectReview
dc.subjectSymbiosis
dc.subjectT lymphocyte
dc.titleTargeted therapies for inflammatory bowel disease and colorectal cancer: An increasing need for microbiota-intestinal mutualism
dc.typeReview

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