Gut microbiota imbalance and colorectal cancer
The gut microbiota acts as a real organ. The symbioticinteractions between resident micro-organisms and thedigestive tract highly contribute to maintain the guthomeostasis. However, alterations to the microbiomecaused by environmental changes (e.g. , infection, dietand/or lifestyle) can disturb this...
Gespeichert in:
Veröffentlicht in: | World journal of gastroenterology : WJG 2016-01, Vol.22 (2), p.501-518 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The gut microbiota acts as a real organ. The symbioticinteractions between resident micro-organisms and thedigestive tract highly contribute to maintain the guthomeostasis. However, alterations to the microbiomecaused by environmental changes (e.g. , infection, dietand/or lifestyle) can disturb this symbiotic relationshipand promote disease, such as inflammatory boweldiseases and cancer. Colorectal cancer is a complexassociation of tumoral cells, non-neoplastic cells and alarge amount of micro-organisms, and the involvementof the microbiota in colorectal carcinogenesis isbecoming increasingly clear. Indeed, many changes inthe bacterial composition of the gut microbiota havebeen reported in colorectal cancer, suggesting a majorrole of dysbiosis in colorectal carcinogenesis. Somebacterial species have been identified and suspectedto play a role in colorectal carcinogenesis, such asStreptococcus bovis , Helicobacter pylori , Bacteroides fragilis , Enterococcus faecalis , Clostridium septicum ,Fusobacterium spp. and Escherichia coli . The potentialpro-carcinogenic effects of these bacteria are nowbetter understood. In this review, we discuss thepossible links between the bacterial microbiota andcolorectal carcinogenesis, focusing on dysbiosis andthe potential pro-carcinogenic properties of bacteria,such as genotoxicity and other virulence factors,inflammation, host defenses modulation, bacterialderivedmetabolism, oxidative stress and antioxidativedefenses modulation. We lastly describehow bacterial microbiota modifications could representnovel prognosis markers and/or targets for innovativetherapeutic strategies. |
---|---|
ISSN: | 1007-9327 2219-2840 |
DOI: | 10.3748/wjg.v22.i2.501 |