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. Author manuscript; available in PMC: 2021 Jan 1.
Published in final edited form as: Gastroenterology. 2019 Oct 3;158(2):322–340. doi: 10.1053/j.gastro.2019.06.048

Table 2.

Microbes Associated With Increased or Reduced Risk of CRC

Microbe Epidemiologic Evidence Potential mechanisms References
Associated with higher risk of CRC
Fusobacterium nucleatum Enriched tumor tissue; higher fecal abundance in patients with colorectal neoplasia than controls; associated with advanced cancer stage, lower infiltration by T cells, higher risk of recurrence, and poorer patient survival; correlated with the molecular characteristics of the serrated pathway. Promotion of a tumor-permissive microenvironment through recruitment of myeloidderived suppressor cells and inhibition of antitumor defense by NK or T cells; modulation of Ecadherin/β-catenin. 21, 22, 140, 219
 Enterotoxigenic Bacteroides fragilis (ETBF) Enriched in tumor tissue and fecal samples of CRC patients; associated with advanced cancer stage and proximal colon tumor. DNA damage 40, 220, 221
pks+ Escherichia coli More frequently detected in individuals with than without CRC, more frequently in tumors than in normal flanking tissue, and more frequently in late-stage tumors than in early-stage tumors. Promotion of intestinal inflammation 49, 222
Associated with lower risk of CRC
 SCFA-producing bacteria Lower abundance in CRC patients than bacteria controls; higher abundance in Native Americans with a low CRC incidence; associated with improved immune response and better metabolic parameters. Metabolic and immune modulation of SCFAs that protects against CRC. 124, 128, 223