publication . Article . 2018

Oral Bacterial and Fungal Microbiome Impacts Colorectal Carcinogenesis

Klimešová, K. (Klára); Zákostelská, Z. (Zuzana); Tlaskalová-Hogenová, H. (Helena);
Open Access English
  • Published: 01 Apr 2018 Journal: Frontiers in Microbiology, volume 9 (eissn: 1664-302X, Copyright policy)
  • Publisher: Frontiers Media S.A.
  • Country: Czech Republic
Abstract
Host's physiology is significantly influenced by microbiota colonizing the epithelial surfaces. Complex microbial communities contribute to proper mucosal barrier function, immune response, and prevention of pathogen invasion and have many other crucial functions. The oral cavity and large intestine are distant parts of the digestive tract, both heavily colonized by commensal microbiota. Nevertheless, they feature different proportions of major bacterial and fungal phyla, mostly due to distinct epithelial layers organization and different oxygen levels. A few obligate anaerobic strains inhabiting the oral cavity are involved in the pathogenesis of oral diseases....
Subjects
Medical Subject Headings: stomatognathic diseases
free text keywords: Microbiology, Review, microbiome, mycobiome, pathobiont, dysbiosis, biofilm, Fusobacterium, oral diseases, QR1-502, Microbiology (medical), Pathogen, Biology, Immune system, Obligate, biology.organism_classification, Barrier function, medicine.disease, medicine
Related Organizations
141 references, page 1 of 10

Aagaard K.Ma J.Antony K. M.Ganu R.Petrosino J.Versalovic J. (2014). The placenta harbors a unique microbiome. Sci. Transl. Med. 6:237ra65. 10.1126/scitranslmed.3008599 24848255 [OpenAIRE] [PubMed] [DOI]

Aas J. A.Paster B. J.Stokes L. N.Olsen I.Dewhirst F. E. (2005). Defining the normal bacterial flora of the oral cavity. J. Clin. Microbiol. 43 5721–5732. 10.1128/Jcm.43.11.5721-5732.2005 16272510 [OpenAIRE] [PubMed] [DOI]

Abed J.Emgard J. E. M.Zamir G.Faroja M.Almogy G.Grenov A. (2016). Fap2 mediates Fusobacterium nucleatum colorectal adenocarcinoma enrichment by binding to tumor-expressed Gal-GalNAc. Cell Host Microbe 20 215–225. 10.1016/j.chom.2016.07.006 27512904 [OpenAIRE] [PubMed] [DOI]

Abreu M. T. (2010). Toll-like receptor signalling in the intestinal epithelium: how bacterial recognition shapes intestinal function. Nat. Rev. Immunol. 10 131–144. 10.1038/nri2707 20098461 [OpenAIRE] [PubMed] [DOI]

Adlerberth I.Wold A. E. (2009). Establishment of the gut microbiota in Western infants. Acta Paediatr. 98 229–238. 10.1111/j.1651-2227.2008.01060.x 19143664 [OpenAIRE] [PubMed] [DOI]

Amitay E. L.Werner S.Vital M.Pieper D. H.Hofler D.Gierse I. J. (2017). Fusobacterium and colorectal cancer: causal factor or passenger? Results from a large colorectal cancer screening study. Carcinogenesis 38 781–788. 10.1093/carcin/bgx053 28582482 [OpenAIRE] [PubMed] [DOI]

Arthur J. C.Jobin C. (2011). The struggle within: microbial influences on colorectal cancer. Inflamm. Bowel Dis. 17 396–409. 10.1002/ibd.21354 20848537 [OpenAIRE] [PubMed] [DOI]

Arthur J. C.Perez-Chanona E.Muhlbauer M.Tomkovich S.Uronis J. M.Fan T. J. (2012). Intestinal inflammation targets cancer-inducing activity of the microbiota. Science 338 120–123. 10.1126/science.1224820 22903521 [OpenAIRE] [PubMed] [DOI]

Arumugam M.Raes J.Pelletier E.Le Paslier D.Yamada T.Mende D. R. (2011). Enterotypes of the human gut microbiome. Nature 473 174–180. 10.1038/nature09944 21508958 [OpenAIRE] [PubMed] [DOI]

Backhed F.Fraser C. M.Ringel Y.Sanders M. E.Sartor R. B.Sherman P. M. (2012). Defining a healthy human gut microbiome: current concepts, future directions, and clinical applications. Cell Host Microbe 12 611–622. 10.1016/j.chom.2012.10.012 23159051 [OpenAIRE] [PubMed] [DOI]

Bank S.Andersen P. S.Burisch J.Pedersen N.Roug S.Galsgaard J. (2015). Polymorphisms in the toll-like receptor and the IL-23/IL-17 pathways were associated with susceptibility to inflammatory bowel disease in a danish cohort. PLoS One 10:e0145302. 10.1371/journal.pone.0145302 26698117 [OpenAIRE] [PubMed] [DOI]

Bankvall M.Sjoberg F.Gale G.Wold A.Jontell M.Ostman S. (2014). The oral microbiota of patients with recurrent aphthous stomatitis. J. Oral Microbiol. 6:25739. 10.3402/Jom.V6.25739 25626771 [OpenAIRE] [PubMed] [DOI]

Bartova J.Sommerova P.Lyuya-Mi Y.Mysak J.Prochazkova J.Duskova J. (2014). Periodontitis as a risk factor of atherosclerosis. J. Immunol. Res. 2014:636893. 10.1155/2014/636893 24741613 [OpenAIRE] [PubMed] [DOI]

Blazkova H.Krejcikova K.Moudry P.Frisan T.Hodny Z.Bartek J. (2010). Bacterial intoxication evokes cellular senescence with persistent DNA damage and cytokine signalling. J. Cell Mol. Med. 14 357–367. 10.1111/j.1582-4934.2009.00862.x 19650831 [OpenAIRE] [PubMed] [DOI]

Boursi B.Haynes K.Mamtani R.Yang Y. X. (2015). Impact of antibiotic expos ure on the risk of colorectal cancer. Pharmacoepidemiol. Drug Saf. 24 534–542. 10.1002/pds.3765 25808540 [OpenAIRE] [PubMed] [DOI]

141 references, page 1 of 10
Abstract
Host's physiology is significantly influenced by microbiota colonizing the epithelial surfaces. Complex microbial communities contribute to proper mucosal barrier function, immune response, and prevention of pathogen invasion and have many other crucial functions. The oral cavity and large intestine are distant parts of the digestive tract, both heavily colonized by commensal microbiota. Nevertheless, they feature different proportions of major bacterial and fungal phyla, mostly due to distinct epithelial layers organization and different oxygen levels. A few obligate anaerobic strains inhabiting the oral cavity are involved in the pathogenesis of oral diseases....
Subjects
Medical Subject Headings: stomatognathic diseases
free text keywords: Microbiology, Review, microbiome, mycobiome, pathobiont, dysbiosis, biofilm, Fusobacterium, oral diseases, QR1-502, Microbiology (medical), Pathogen, Biology, Immune system, Obligate, biology.organism_classification, Barrier function, medicine.disease, medicine
Related Organizations
141 references, page 1 of 10

Aagaard K.Ma J.Antony K. M.Ganu R.Petrosino J.Versalovic J. (2014). The placenta harbors a unique microbiome. Sci. Transl. Med. 6:237ra65. 10.1126/scitranslmed.3008599 24848255 [OpenAIRE] [PubMed] [DOI]

Aas J. A.Paster B. J.Stokes L. N.Olsen I.Dewhirst F. E. (2005). Defining the normal bacterial flora of the oral cavity. J. Clin. Microbiol. 43 5721–5732. 10.1128/Jcm.43.11.5721-5732.2005 16272510 [OpenAIRE] [PubMed] [DOI]

Abed J.Emgard J. E. M.Zamir G.Faroja M.Almogy G.Grenov A. (2016). Fap2 mediates Fusobacterium nucleatum colorectal adenocarcinoma enrichment by binding to tumor-expressed Gal-GalNAc. Cell Host Microbe 20 215–225. 10.1016/j.chom.2016.07.006 27512904 [OpenAIRE] [PubMed] [DOI]

Abreu M. T. (2010). Toll-like receptor signalling in the intestinal epithelium: how bacterial recognition shapes intestinal function. Nat. Rev. Immunol. 10 131–144. 10.1038/nri2707 20098461 [OpenAIRE] [PubMed] [DOI]

Adlerberth I.Wold A. E. (2009). Establishment of the gut microbiota in Western infants. Acta Paediatr. 98 229–238. 10.1111/j.1651-2227.2008.01060.x 19143664 [OpenAIRE] [PubMed] [DOI]

Amitay E. L.Werner S.Vital M.Pieper D. H.Hofler D.Gierse I. J. (2017). Fusobacterium and colorectal cancer: causal factor or passenger? Results from a large colorectal cancer screening study. Carcinogenesis 38 781–788. 10.1093/carcin/bgx053 28582482 [OpenAIRE] [PubMed] [DOI]

Arthur J. C.Jobin C. (2011). The struggle within: microbial influences on colorectal cancer. Inflamm. Bowel Dis. 17 396–409. 10.1002/ibd.21354 20848537 [OpenAIRE] [PubMed] [DOI]

Arthur J. C.Perez-Chanona E.Muhlbauer M.Tomkovich S.Uronis J. M.Fan T. J. (2012). Intestinal inflammation targets cancer-inducing activity of the microbiota. Science 338 120–123. 10.1126/science.1224820 22903521 [OpenAIRE] [PubMed] [DOI]

Arumugam M.Raes J.Pelletier E.Le Paslier D.Yamada T.Mende D. R. (2011). Enterotypes of the human gut microbiome. Nature 473 174–180. 10.1038/nature09944 21508958 [OpenAIRE] [PubMed] [DOI]

Backhed F.Fraser C. M.Ringel Y.Sanders M. E.Sartor R. B.Sherman P. M. (2012). Defining a healthy human gut microbiome: current concepts, future directions, and clinical applications. Cell Host Microbe 12 611–622. 10.1016/j.chom.2012.10.012 23159051 [OpenAIRE] [PubMed] [DOI]

Bank S.Andersen P. S.Burisch J.Pedersen N.Roug S.Galsgaard J. (2015). Polymorphisms in the toll-like receptor and the IL-23/IL-17 pathways were associated with susceptibility to inflammatory bowel disease in a danish cohort. PLoS One 10:e0145302. 10.1371/journal.pone.0145302 26698117 [OpenAIRE] [PubMed] [DOI]

Bankvall M.Sjoberg F.Gale G.Wold A.Jontell M.Ostman S. (2014). The oral microbiota of patients with recurrent aphthous stomatitis. J. Oral Microbiol. 6:25739. 10.3402/Jom.V6.25739 25626771 [OpenAIRE] [PubMed] [DOI]

Bartova J.Sommerova P.Lyuya-Mi Y.Mysak J.Prochazkova J.Duskova J. (2014). Periodontitis as a risk factor of atherosclerosis. J. Immunol. Res. 2014:636893. 10.1155/2014/636893 24741613 [OpenAIRE] [PubMed] [DOI]

Blazkova H.Krejcikova K.Moudry P.Frisan T.Hodny Z.Bartek J. (2010). Bacterial intoxication evokes cellular senescence with persistent DNA damage and cytokine signalling. J. Cell Mol. Med. 14 357–367. 10.1111/j.1582-4934.2009.00862.x 19650831 [OpenAIRE] [PubMed] [DOI]

Boursi B.Haynes K.Mamtani R.Yang Y. X. (2015). Impact of antibiotic expos ure on the risk of colorectal cancer. Pharmacoepidemiol. Drug Saf. 24 534–542. 10.1002/pds.3765 25808540 [OpenAIRE] [PubMed] [DOI]

141 references, page 1 of 10
Powered by OpenAIRE Open Research Graph
Any information missing or wrong?Report an Issue
publication . Article . 2018

Oral Bacterial and Fungal Microbiome Impacts Colorectal Carcinogenesis

Klimešová, K. (Klára); Zákostelská, Z. (Zuzana); Tlaskalová-Hogenová, H. (Helena);