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

被引:95
作者
Abu-Ghazaleh, Nadine [1 ]
Chua, Weng Joe [1 ]
Gopalan, Vinod [1 ]
机构
[1] Griffith Univ, Menzies Hlth Inst Queensland, Sch Med, Gold Coast Campus, Gold Coast, NSW, Australia
关键词
Bacteroides fragilis; bile acids; colorectal cancer; diet; dysbiosis; Escherichia coli; Fusobacterium nucleatum; microbiota; processed meat; Streptococcus gallolyticus subsp; gallolyticus (Sgg); FOOD-BORNE CARCINOGEN; COLORECTAL-CANCER; FUSOBACTERIUM-NUCLEATUM; GUT MICROBIOTA; ESCHERICHIA-COLI; RED MEAT; PROTEIN; HEME; HYPERPROLIFERATION; TUMORIGENESIS;
D O I
10.1111/jgh.15042
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:75 / 88
页数:14
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