Literature DB >> 33263888

Microbial Metabolites as Molecular Mediators of Host-Microbe Symbiosis in Colorectal Cancer.

N P Hyland1,2, A Houston3,4, J M Keane3,5,4, S A Joyce3,6, C G M Gahan3,5,7.   

Abstract

The symbiosis between the gut microbiota and the host has been identified as an integral part of normal human physiology and physiological development. Research in germ-free or gnotobiotic animals has demonstrated the importance of this symbiosis in immune, vascular, hepatic, respiratory and metabolic systems. Disruption of the microbiota can also contribute to disease, and the microbiota has been implicated in numerous intestinal and extra-intestinal pathologies including colorectal cancer. Interactions between host and microbiota can occur either directly or indirectly, via microbial-derived metabolites. In this chapter, we focus on two major products of microbial metabolism, short-chain fatty acids and bile acids, and their role in colorectal cancer. Short-chain fatty acids are the products of microbial fermentation of complex carbohydrates and confer protection against cancer risk, while bile acids are compounds which are endogenous to the host, but undergo microbial modification in the large intestine leading to alterations in their bioactivity. Lastly, we discuss the ability of microbial modulation to mediate cancer risk and the potential to harness this ability as a prophylactic or therapeutic treatment in colorectal cancer.

Entities:  

Keywords:  Bile; Butyrate; Colon; Gut microbiota; Tumorigenesis

Mesh:

Year:  2020        PMID: 33263888     DOI: 10.1007/978-3-030-51849-3_22

Source DB:  PubMed          Journal:  Results Probl Cell Differ        ISSN: 0080-1844


  158 in total

1.  Potential of short chain fatty acids to modulate the induction of DNA damage and changes in the intracellular calcium concentration by oxidative stress in isolated rat distal colon cells.

Authors:  S L Abrahamse; B L Pool-Zobel; G Rechkemmer
Journal:  Carcinogenesis       Date:  1999-04       Impact factor: 4.944

2.  Effect of intestinal bacteria on formation of azoxymethane-induced aberrant crypt foci in the rat colon.

Authors:  H Arimochi; T Kinouchi; K Kataoka; T Kuwahara; Y Ohnishi
Journal:  Biochem Biophys Res Commun       Date:  1997-09-29       Impact factor: 3.575

3.  Human gut microbiome and risk for colorectal cancer.

Authors:  Jiyoung Ahn; Rashmi Sinha; Zhiheng Pei; Christine Dominianni; Jing Wu; Jianxin Shi; James J Goedert; Richard B Hayes; Liying Yang
Journal:  J Natl Cancer Inst       Date:  2013-12-06       Impact factor: 13.506

4.  A "field change" of inhibited apoptosis occurs in colorectal mucosa adjacent to colorectal adenocarcinoma.

Authors:  S Badvie; A Hanna-Morris; H J N Andreyev; P Cohen; S Saini; T G Allen-Mersh
Journal:  J Clin Pathol       Date:  2006-05-05       Impact factor: 3.411

5.  Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer.

Authors:  Ramadass Balamurugan; Ethendhar Rajendiran; Sarah George; G Vijay Samuel; Balakrishnan S Ramakrishna
Journal:  J Gastroenterol Hepatol       Date:  2008-07-08       Impact factor: 4.029

6.  Effect of dairy products on initiation of precursor lesions of colon cancer in rats.

Authors:  H Abdelali; P Cassand; V Soussotte; M Daubeze; C Bouley; J F Narbonne
Journal:  Nutr Cancer       Date:  1995       Impact factor: 2.900

7.  Emergence of permanently differentiated cell clones in a human colonic cancer cell line in culture after treatment with sodium butyrate.

Authors:  C Augeron; C L Laboisse
Journal:  Cancer Res       Date:  1984-09       Impact factor: 12.701

8.  Butyrate rapidly induces growth inhibition and differentiation in HT-29 cells.

Authors:  J A Barnard; G Warwick
Journal:  Cell Growth Differ       Date:  1993-06

9.  Mitotic aneuploidy induced by sodium deoxycholate in Aspergillus nidulans.

Authors:  S J Assinder; A Upshall
Journal:  Mutat Res       Date:  1982-03       Impact factor: 2.433

10.  Unconjugated secondary bile acids in the serum of patients with colorectal adenomas.

Authors:  E Bayerdörffer; G A Mannes; T Ochsenkühn; P Dirschedl; B Wiebecke; G Paumgartner
Journal:  Gut       Date:  1995-02       Impact factor: 23.059

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