Intestinal microbiota and its association with colon cancer and red/processed meat consumption

• Published in: Journal of gastroenterology and hepatology Vol. 36; no. 1; pp. 75 - 88
• Main Authors: Abu‐Ghazaleh, Nadine, Chua, Weng Joe, Gopalan, Vinod
• Format: Journal Article
• Language: English
• Published: Australia Wiley Subscription Services, Inc 01-01-2021
• Subjects: Adenocarcinoma; Adenoma; Amines; Angiogenesis; Bacteroides fragilis; bile acids; Carcinogenesis; Colon; Colon cancer; colorectal cancer; Colorectal carcinoma; diet; Dysbacteriosis; dysbiosis; Escherichia coli; Fusobacterium nucleatum; Genotoxicity; Heme; Heterocyclic amines; Intestinal microflora; Intestine; Meat; Metabolomics; Microbiomes; Microbiota; Microorganisms; processed meat; Streptococcus gallolyticus subsp. gallolyticus (Sgg); Tumor suppressor genes; Tumorigenesis; microbiota; colorectal cancer; Fusobacterium nucleatum; Bacteroides fragilis; Streptococcus gallolyticus subsp. gallolyticus (Sgg); bile acids; Escherichia coli; processed meat; diet; dysbiosis
• ISSN: 0815-9319; 1440-1746
• DOI: 10.1111/jgh.15042

The human colon harbors a high number of microorganisms that were reported to play a crucial role in colorectal carcinogenesis. In the recent decade, molecular detection and metabolomic techniques have expanded our knowledge on the role of specific microbial species in promoting tumorigenesis. In this study, we reviewed the association between microbial dysbiosis and colorectal carcinoma (CRC). Various microbial species and their association with colorectal tumorigenesis and red/processed meat consumption have been reviewed. The literature demonstrated a significant abundance of Fusobacterium nucleatum, Streptococcus bovis/gallolyticus, Escherichia coli, and Bacteroides fragilis in patients with adenoma or adenocarcinoma compared to healthy individuals. The mechanisms in which each organism was postulated to promote colon carcinogenesis were collated and summarized in this review. These include the microorganisms' ability to adhere to colon cells; modulate the inhibition of tumor suppressor genes, the activations of oncogenes, and genotoxicity; and activate downstream targets responsible for angiogenesis. The role of these microorganisms in conjugation with meat components including N‐nitroso compounds, heterocyclic amines, and heme was also evident in multiple studies. The outcome of this review supports the role of red meat consumption in modulating CRC progression and the possibility of gut microbiome influencing the relationship between CRC and diet. The study also demonstrates that microbiota analysis could potentially complement existing screening methods when detecting colonic lesions.