Intestinal Inflammation Targets Cancer-Inducing Activity of the Microbiota

Janelle C. Arthur(University of North Carolina at Chapel Hill), Ernesto Peréz-Chanona(University of North Carolina at Chapel Hill), Marcus Mühlbauer(University of North Carolina at Chapel Hill), Sarah Tomkovich(University of North Carolina at Chapel Hill), Joshua M. Uronis(University of North Carolina at Chapel Hill), Ting-Jia Fan(University of North Carolina at Chapel Hill), Barry J. Campbell(University of Liverpool), Turki S. Abujamel(University of Ottawa), Belgin Dogan(Cornell University), Arlin B. Rogers(University of North Carolina at Chapel Hill), Jonathan M. Rhodes(University of Liverpool), Alain Stintzi(University of Ottawa), Kenneth W. Simpson(Cornell University), Jonathan J. Hansen(University of North Carolina at Chapel Hill), Temitope O. Keku(University of North Carolina at Chapel Hill), Anthony A. Fodor(University of North Carolina at Charlotte), Christian Jobin(University of North Carolina at Chapel Hill)
Science
August 17, 2012
Cited by 2,219Open Access
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Abstract

Inflammation alters host physiology to promote cancer, as seen in colitis-associated colorectal cancer (CRC). Here, we identify the intestinal microbiota as a target of inflammation that affects the progression of CRC. High-throughput sequencing revealed that inflammation modifies gut microbial composition in colitis-susceptible interleukin-10-deficient (Il10(-/-)) mice. Monocolonization with the commensal Escherichia coli NC101 promoted invasive carcinoma in azoxymethane (AOM)-treated Il10(-/-) mice. Deletion of the polyketide synthase (pks) genotoxic island from E. coli NC101 decreased tumor multiplicity and invasion in AOM/Il10(-/-) mice, without altering intestinal inflammation. Mucosa-associated pks(+) E. coli were found in a significantly high percentage of inflammatory bowel disease and CRC patients. This suggests that in mice, colitis can promote tumorigenesis by altering microbial composition and inducing the expansion of microorganisms with genotoxic capabilities.


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