| Literature DB >> 29420293 |
Christine M Dejea1,2, Payam Fathi1,2,3, John M Craig4, Annemarie Boleij1,5, Rahwa Taddese5, Abby L Geis1,2, Xinqun Wu1,3, Christina E DeStefano Shields1,2, Elizabeth M Hechenbleikner6, David L Huso7, Robert A Anders8, Francis M Giardiello2,3, Elizabeth C Wick6, Hao Wang1,2, Shaoguang Wu1,3, Drew M Pardoll1,2, Franck Housseau1,2, Cynthia L Sears9,2,3.
Abstract
Individuals with sporadic colorectal cancer (CRC) frequently harbor abnormalities in the composition of the gut microbiome; however, the microbiota associated with precancerous lesions in hereditary CRC remains largely unknown. We studied colonic mucosa of patients with familial adenomatous polyposis (FAP), who develop benign precursor lesions (polyps) early in life. We identified patchy bacterial biofilms composed predominately of Escherichia coli and Bacteroides fragilis Genes for colibactin (clbB) and Bacteroides fragilis toxin (bft), encoding secreted oncotoxins, were highly enriched in FAP patients' colonic mucosa compared to healthy individuals. Tumor-prone mice cocolonized with E. coli (expressing colibactin), and enterotoxigenic B. fragilis showed increased interleukin-17 in the colon and DNA damage in colonic epithelium with faster tumor onset and greater mortality, compared to mice with either bacterial strain alone. These data suggest an unexpected link between early neoplasia of the colon and tumorigenic bacteria.Entities:
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Year: 2018 PMID: 29420293 PMCID: PMC5881113 DOI: 10.1126/science.aah3648
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728